HealthMasters Christmas Show

Show Description:

Must listen!

Ok - this show is probably the clearest most succinct show that I have done concerning the following topics. It is a must listen high energy show! It ties these topics together!

The Multidimensional fractal universe.

What is the purpose of black magic?

Why is there an atavistic hatred of Christ?

Who are the four horseman of banking?

Who owns the world? What is Babylonian money magic?

What is the threshold at CERN?

What is the Veil?

How does The Blood of Christ save us?

How is Jesus the Passover Lamb of God?

What does it really do when you accept Christ?

How should Christians live?

Why have contemporary churches many times removed the Blood of Christ songs?

Are they preaching the real Jesus?

What is an inter-dimensional interface?

Why is the third temple being rebuilt?

Yes this is that show! A lot of new information. This is a high energy must listen broadcast!

Hosts: Ted & Austin Broer
http://mediaarchives.gsradio.net/Ted_Broer/122519.mp3

Jim Stone Offers A Solution To The Vaccine "Problem"

HERE IS THE SOLUTION TO THE VACCINE PROBLEM

There is a despicable (replacing the original word used with SCUMBAG) who has released a major report about how YES, vaccines are triggering auto immune disorders and autism, and then he blames it all on ALUMINUM!!!!!!!!! What more do you expect?


Here is the solution: Ban ALL vaccines grown in human tissue cultures, and ban ALL vaccines that use adjuvants. How do you turn a small batch of legitimate vaccines that seldom did harm (like what we had 40+ years ago) into a huge profit making shipment that cost practically nothing, but still triggers an immune response?


ANSWER: Mix it with adjuvants - materials that cause the immune system to act against the small amount of legitimate vaccine strongly. So what if it is a critical material like Squalene, or something else the body uses as a basic building block? If you make more money and you are a total prick, one kid out of 50 being completely wiped out by autism is completely worth it, and 20 or so more out of that 50 that get nailed by auto immune disorders will be there in your pocket for life, filling it with money, buying more of your products to help them deal with the destruction you caused! Come on now, there are LOTS of people who think that way! What about the crack head who rips apart a $3,000 vending machine to get to a coin box that has $20 in it? Who cares if you do totally disproportionate damage to get a little cash if it never comes back to haunt you! And if you own the repair shop that fixes the vending machines, it would pay even more to go out and steal a few coin boxes yourself! THAT is the state of American medical. And if any report you read does not say anything about BIOLIGICAL adjuvants and human tissue and/or GMO viruses in vaccines doing the damage, no matter how well it approaches the truth, if it points at a different culprit it is a SCAM REPORT PURE AND SIMPLE, which is intentionally done to drive people away from the real reasons why vaccines are so damaging.


If the tribe can keep us diverted long enough, TRIBE CAN GET THEIR ULTIMATE VICTORY BY DESTROYING SO MANY OF US THAT WE ARE TOO CRIPPLED TO EVER ACCOMPLISH ANYTHING OF SUBSTANCE AGAIN. This is exactly one such report that I am talking about, the publisher is either rock stupid or a complete fraud! Yep, you'll NEVER see Google, Facebook, or the MSM come out against this report, because it is a diversion down a cattle trail and off a cliff! QUESTION: How can a "toxic metal" trigger an auto immune response against a key oil, protein, or cell structure? Answer: Despite the magnificent word wrangling and spewing of terms to explain it, IT CAN'T, and therefore the entire "auto immune" premise of that report is fraudulent. The only thing a toxic metal can do is DIRECT DAMAGE, that will most likely heal at least partially later.


Obviously I would not want mercury or aluminum injected into me, but I'd sure as HELL take that before I'd accept a genetically engineered attack virus or human tissue that will trigger a permanent and unrecoverable auto immune caused brain disorder, or a biologically based adjuvant that will do the same! The report says not one word about fetal cell cultures, biological adjuvants, or GMO attack viruses. All of this is provably in vaccines, and all of those are provably potentially destructive. If it does not utter a peep about that while talking about auto immune disorders, it is absolutely FRAUDULENT.


Fact: Vaccines that use peanut oil as an adjuvant will trigger peanut allergies in many people who get vaccinated with a vaccine that uses it. Vaccines grown in animal tissue can trigger allergies to dogs and cats. And vaccines grown in human tissue can trigger an immune reaction against yourself, that's a no brainer, and if you get shot up enough, you will probably not have a brain. You simply cannot inject a pathogen in the presence of any foreign human material and expect consistent, good results! My reports on this are just as certified as any Jewish doctor spewing lies and diversions, because my reports are backed up by similarly papered people, which in my case are not the enemy! Just because a web site has "green" in the title and claims to be alternative/wholistic does not mean it is not set up as a false front to push outrageous well worded fraud!


I'm having so much fun on MINDS! You really should join in the fun and education! I want to get serious regarding a clear and present danger: NAGALASE.

Nagalase is the compound directly responsible for the discomfort one feels when inflammation occurs. When the body requires Vitamin D3 in response to an immune trigger, and doesn't receive it, it instead converts the infection-fighting enzymes into nagalase, which in turn, triggers cytokines storms. You should really hear Dr. Ted Broer tell it:

Former Pro-GMO Biotech Scientist Admits GMOs are NOT Safe (Re-Post from HealthMasters)

Let's start with a piece from Austin Broer, Ted Broer's son and co-host on the HealthMasters podcast, as well as the HealthMasters store.

Former Pro-GMO Biotech Scientist Admits GMOs are NOT Safe

Submitted by Austin Broer on Fri, 07/22/2016 - 17:26

Dr. Thierry Vrain  A former GMO biotechnologist who has come out with a lot of information that should open people’s eyes about the real dangers of genetically modified foods and crops.

Vrain will be the first to admit that Monsanto has conducted a lot of studies showing that GMOs are safe, but he changed his own tune about ten years ago when he started reading scientific journals from other countries.

Vrain explains:

“I started paying attention to the flow of published studies coming from Europe, some from prestigious labs and published in prestigious scientific journals, that questioned the impact and safety of engineered food.”

Vrain was so much a supporter of GMOs (as well as a former biotech scientist for Agriculture Canada) that he used to conduct tours and tell large groups of people all about the greatness of genetically altered crops – but not anymore. Here is what he thinks about his former industry now:

“I refute the claims of the biotechnology companies that their engineered crops yield more, that they require less pesticide applications, that they have no impact on the environment and of course that they are safe to eat.

There are a number of scientific studies that have been done for Monsanto by universities in the U.S., Canada, and abroad. Most of these studies are concerned with the field performance of the engineered crops, and of course they find GMOs safe for the environment and therefore safe to eat.”

Vrain thinks the public is being swindled. He believes we should all demand that government agencies replicate tests showing that GMOs are safe rather than rely on studies paid for by the biotech companies. He continues:

“The Bt corn and soya plants that are now everywhere in our environment are registered as insecticides. But are these insecticidal plants regulated and have their proteins been tested for safety? Not by the federal departments in charge of food safety, not in Canada and not in the U.S.

There are no long-term feeding studies performed in these countries to demonstrate the claims that engineered corn and soya are safe. All we have are scientific studies out of Europe and Russia, showing that rats fed engineered food die prematurely.

These studies show that proteins produced by engineered plants are different than what they should be. Inserting a gene in a genome using this technology can and does result in damaged proteins. The scientific literature is full of studies showing that engineered corn and soya contain toxic or allergenic proteins.”

This science is actually only about 40 years old. It is all based on a theory of genetic manipulation hypothesized around 70 years ago – of the ONE GENE – meaning that each gene codes for one single protein. The Human Genome project proved this totally wrong.

Most scientists now understand that any gene can give more than one protein and that inserting a gene anywhere in a plant eventually creates rogue proteins. Some of these proteins are obviously allergenic or toxic, like Cry proteins found in GMO corn. Otherwise known as Bt toxins (Bacillus thuringiensis), Cry proteins are one of biotech’s answers for ‘safe’ food.

That’s odd; one study found them absolutely toxic for mammalian blood. Dr. Mezzomo says that Cry toxins are deathly for mice. Another study linked them to a higher rate of leukemia. Yet another study conducted at Sherbrooke University Hospital in Quebec found corn’s Bt-toxin in the blood of pregnant women and their babies, as well as in non-pregnant women. These same toxins are also associated with higher levels of inflammation in the body, allergies, MS, and cancer.

Furthermore, what ridiculous egocentricity for biotech scientists to think they can crack the code of life when there are still acres and acres of rainforest that contain medicinal herbs that they have never even studied or recognized. Every square mile lost in these forests represents a possible cancer soution or super-food source.

Why the heck do we need GMOs? We haven’t even utilized the plethora of foods and herbs Mother Nature has already provided us with, if only we would steward them sustainably. There seems to be a new wonder-extract being discovered every few days, despite our pillaging.

Additionally, Vrain once answered honestly to this question in an interview:

“Q: It is astounding that people don’t question the very idea of altering DNA. When Monsanto or others claim a genetically modified organism is “substantially equivalent” to the conventional plant, it’s illogical to me because when DNA is altered, the plant is altered. It’s not the same and it’s certainly not natural.

A: That depends on your view of the world. As a scientist, when you add a bacteria gene to a plant, or a plant gene to a fish, or a human gene to corn, or 10,000 acres of corn growing insulin – they consider it progress. So if a tomato plant has a bacterial gene, it still looks very much like a tomato plant. You couldn’t tell very much from the taste of the tomato so there is something easy about believing in “substantial equivalence” . . . but Roundup (Monsanto’s herbicide) is a chelator; it holds manganese, magnesium and a few other minerals. It holds the minerals and doesn’t let go so basically it starves the plant. It probably also starves many other creatures in the soil.” 

New evidence shows that these same important minerals are chelated from humans that eat RoundUp GMOs.

Vrain has based his research on over 500 government reports and scientific articles published in peer-reviewed journals, some of them with the highest recognition in the world.

Now tell me – how exactly are GMOs safe?

If a soil biologist and scientist of genetic engineering of 30 years revisits his stance on GMOs – shouldn’t those who are still clinging to biotech efficacy relent? We need as many GMO whistleblowers as we can get to come forward and shed light on the real truth about what is being done to our food.

Honestly, I'm spending an inordinate amount of time at MINDS, considering how much more I am able to spread the word about the things in this world that require attention. One thing I intend to do is to fact-check vitamin companies and ask as to why certain things are present in our vitamins. For example, why would Walgreens use sucralose in their version of Emergen-C product? Wouldn't that simply negate any positive aspects whatsoever?

There are Vitamin D products that use calcium carbonate, which for humans, is the equivalent of chowing down seashells from the beach. The human body cannot break it down, so you can't be possibly getting any benefit at all from the product. Check your labels.

Now, just because you may wish to ignore politics, doesn't mean that politics will ignore YOU.

James O'Keefe's explosive video:

"Hillary's America: The Secret History of the Democratic Party" 06/2016 (Dinesh D'Souza)

Published on Jul 5, 2016

NYT best-selling author and filmmaker Dinesh D'Souza spoke to a sold out crowd of conservative students at YAF's High School Conference at the Reagan Ranch.

# More "Voices of Reason":
https://www.youtube.com/playlist?list...
# Subscribe:
https://www.youtube.com/channel/UCcM3...

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• Rumours are that, if Hillary Diane Rodham Clinton cannot challenge Donald John Trump on Tuesday, November 8, 20016, that she will be replaced with...Michelle Obama.

There were additional mergers of biotech companies, by the way...listen to the HealthMasters show to get the details.

dr. Ted Broer on the Hagmann and Hagmann Report 08/26/2016

Lot of stuff going on, but for now, enjoy these three hours of Dr. Ted Broer on the Hagmann and Hagmann Report.

https://itunes.apple.com/us/podcast/hagmann-hagmann-report/id631558915?mt=2#episodeGuid=http%3A%2F%2Fwww.blogtalkradio.com%2Fcfp-radio%2F2016%2F08%2F26%2Fbreaking-news-with-dr-ted-broer-on-the-hagmann-hagmann-report

Health Is A Racket

Our health has been monetized.

There are very conscientious individuals in the field, but they are fighting against those who wish to manage our lives by addressing symptoms, rather than going to the root of the issue.

Of course, one needs to understand that health care has become an industry. It's now all about keeping you and I on myriad pills and concoctions, keeping their pockets well fed as we attempt to make it from our beds and face the ongoing maladies.

There are cures for cancer.

There are cures for diabetes.

There are cures for practically everything...but that doesn't keep the health machine fed.

Cost-benefit analyses are conducted to test the viability of their concoctions, and commercials are subtexted with serene scenery and imagery to obfuscate the verbiage that warns us of the potential dangers of their offerings.

We need a reform.

Remember laetrile? It was outlawed...but it seems to now be making a comeback.

How many other outlawed cures will we see, now that the mythology is being challenged?

I'm going to re-post the honorable General Smedley Darlington Butler's speech, War Is A Racket, following shortly.

Please listen to Ted and Austin Broer's broadcast from yesterday. If you can't wait for it, go to minute 51, and listen to the actions designed to nullify the GMO labeling laws passed in Vermont.

We need to be constantly vigilant. The bastards want for us to consume their FrankenFoods and slowly wither away mentally, physically and psychologically, while they enjoy REAL FOOD. We are actually losing the right to grow our own foods!



In this day and age, can you believe that?!?

Prejudiced against Italians...but I digress.

                              War Is A Racket

                      By Major General Smedley Butler




                                  Contents

                    Chapter 1: War Is A Racket

                    Chapter 2: Who Makes The Profits?

                    Chapter 3: Who Pays The Bills?

                    Chapter 4: How To Smash This Racket!

                    Chapter 5: To Hell With War!




     Smedley Darlington Butler

        * Born: West Chester, Pa., July 30, 1881
        * Educated: Haverford School
        * Married: Ethel C. Peters, of Philadelphia, June 30, 1905
        * Awarded two congressional medals of honor:
            1. capture of Vera Cruz, Mexico, 1914
            2. capture of Ft. Riviere, Haiti, 1917
        * Distinguished service medal, 1919
        * Major General - United States Marine Corps
        * Retired Oct. 1, 1931
        * On leave of absence to act as
          director of Dept. of Safety, Philadelphia, 1932
        * Lecturer -- 1930's
        * Republican Candidate for Senate, 1932
        * Died at Naval Hospital, Philadelphia, June 21, 1940
        * For more information about Major General Butler,
          contact the United States Marine Corps.




     CHAPTER ONE

     War Is A Racket

     WAR is a racket. It always has been.

     It is possibly the oldest, easily the most profitable, surely the
     most vicious. It is the only one international in scope. It is the
     only one in which the profits are reckoned in dollars and the
     losses in lives.

     A racket is best described, I believe, as something that is not
     what it seems to the majority of the people. Only a small "inside"
     group knows what it is about. It is conducted for the benefit of
     the very few, at the expense of the very many. Out of war a few
     people make huge fortunes.

     In the World War [I] a mere handful garnered the profits of the
     conflict. At least 21,000 new millionaires and billionaires were
     made in the United States during the World War. That many admitted
     their huge blood gains in their income tax returns. How many other
     war millionaires falsified their tax returns no one knows.

     How many of these war millionaires shouldered a rifle? How many of
     them dug a trench? How many of them knew what it meant to go
     hungry in a rat-infested dug-out? How many of them spent
     sleepless, frightened nights, ducking shells and shrapnel and
     machine gun bullets? How many of them parried a bayonet thrust of
     an enemy? How many of them were wounded or killed in battle?

     Out of war nations acquire additional territory, if they are
     victorious. They just take it. This newly acquired territory
     promptly is exploited by the few -- the selfsame few who wrung
     dollars out of blood in the war. The general public shoulders the
     bill.

     And what is this bill?

     This bill renders a horrible accounting. Newly placed gravestones.
     Mangled bodies. Shattered minds. Broken hearts and homes. Economic
     instability. Depression and all its attendant miseries.
     Back-breaking taxation for generations and generations.

     For a great many years, as a soldier, I had a suspicion that war
     was a racket; not until I retired to civil life did I fully
     realize it. Now that I see the international war clouds gathering,
     as they are today, I must face it and speak out.

     Again they are choosing sides. France and Russia met and agreed to
     stand side by side. Italy and Austria hurried to make a similar
     agreement. Poland and Germany cast sheep's eyes at each other,
     forgetting for the nonce [one unique occasion], their dispute over
     the Polish Corridor.

     The assassination of King Alexander of Jugoslavia [Yugoslavia]
     complicated matters. Jugoslavia and Hungary, long bitter enemies,
     were almost at each other's throats. Italy was ready to jump in.
     But France was waiting. So was Czechoslovakia. All of them are
     looking ahead to war. Not the people -- not those who fight and
     pay and die -- only those who foment wars and remain safely at
     home to profit.

     There are 40,000,000 men under arms in the world today, and our
     statesmen and diplomats have the temerity to say that war is not
     in the making.

     Hell's bells! Are these 40,000,000 men being trained to be
     dancers?

     Not in Italy, to be sure. Premier Mussolini knows what they are
     being trained for. He, at least, is frank enough to speak out.
     Only the other day, Il Duce in "International Conciliation," the
     publication of the Carnegie Endowment for International Peace,
     said:

          "And above all, Fascism, the more it considers and
          observes the future and the development of humanity
          quite apart from political considerations of the moment,
          believes neither in the possibility nor the utility of
          perpetual peace. . . . War alone brings up to its
          highest tension all human energy and puts the stamp of
          nobility upon the people who have the courage to meet
          it."

     Undoubtedly Mussolini means exactly what he says. His well-trained
     army, his great fleet of planes, and even his navy are ready for
     war -- anxious for it, apparently. His recent stand at the side of
     Hungary in the latter's dispute with Jugoslavia showed that. And
     the hurried mobilization of his troops on the Austrian border
     after the assassination of Dollfuss showed it too. There are
     others in Europe too whose sabre rattling presages war, sooner or
     later.

     Herr Hitler, with his rearming Germany and his constant demands
     for more and more arms, is an equal if not greater menace to
     peace. France only recently increased the term of military service
     for its youth from a year to eighteen months.

     Yes, all over, nations are camping in their arms. The mad dogs of
     Europe are on the loose. In the Orient the maneuvering is more
     adroit. Back in 1904, when Russia and Japan fought, we kicked out
     our old friends the Russians and backed Japan. Then our very
     generous international bankers were financing Japan. Now the trend
     is to poison us against the Japanese. What does the "open door"
     policy to China mean to us? Our trade with China is about
     $90,000,000 a year. Or the Philippine Islands? We have spent about
     $600,000,000 in the Philippines in thirty-five years and we (our
     bankers and industrialists and speculators) have private
     investments there of less than $200,000,000.

     Then, to save that China trade of about $90,000,000, or to protect
     these private investments of less than $200,000,000 in the
     Philippines, we would be all stirred up to hate Japan and go to
     war -- a war that might well cost us tens of billions of dollars,
     hundreds of thousands of lives of Americans, and many more
     hundreds of thousands of physically maimed and mentally unbalanced
     men.

     Of course, for this loss, there would be a compensating profit --
     fortunes would be made. Millions and billions of dollars would be
     piled up. By a few. Munitions makers. Bankers. Ship builders.
     Manufacturers. Meat packers. Speculators. They would fare well.

     Yes, they are getting ready for another war. Why shouldn't they?
     It pays high dividends.

     But what does it profit the men who are killed? What does it
     profit their mothers and sisters, their wives and their
     sweethearts? What does it profit their children?

     What does it profit anyone except the very few to whom war means
     huge profits?

     Yes, and what does it profit the nation?

     Take our own case. Until 1898 we didn't own a bit of territory
     outside the mainland of North America. At that time our national
     debt was a little more than $1,000,000,000. Then we became
     "internationally minded." We forgot, or shunted aside, the advice
     of the Father of our country. We forgot George Washington's
     warning about "entangling alliances." We went to war. We acquired
     outside territory. At the end of the World War period, as a direct
     result of our fiddling in international affairs, our national debt
     had jumped to over $25,000,000,000. Our total favorable trade
     balance during the twenty-five-year period was about
     $24,000,000,000. Therefore, on a purely bookkeeping basis, we ran
     a little behind year for year, and that foreign trade might well
     have been ours without the wars.

     It would have been far cheaper (not to say safer) for the average
     American who pays the bills to stay out of foreign entanglements.
     For a very few this racket, like bootlegging and other underworld
     rackets, brings fancy profits, but the cost of operations is
     always transferred to the people -- who do not profit.




     CHAPTER TWO

     Who Makes The Profits?

     The World War, rather our brief participation in it, has cost the
     United States some $52,000,000,000. Figure it out. That means $400
     to every American man, woman, and child. And we haven't paid the
     debt yet. We are paying it, our children will pay it, and our
     children's children probably still will be paying the cost of that
     war.

     The normal profits of a business concern in the United States are
     six, eight, ten, and sometimes twelve percent. But war-time
     profits -- ah! that is another matter -- twenty, sixty, one
     hundred, three hundred, and even eighteen hundred per cent -- the
     sky is the limit. All that traffic will bear. Uncle Sam has the
     money. Let's get it.

     Of course, it isn't put that crudely in war time. It is dressed
     into speeches about patriotism, love of country, and "we must all
     put our shoulders to the wheel," but the profits jump and leap and
     skyrocket -- and are safely pocketed. Let's just take a few
     examples:

     Take our friends the du Ponts, the powder people -- didn't one of
     them testify before a Senate committee recently that their powder
     won the war? Or saved the world for democracy? Or something? How
     did they do in the war? They were a patriotic corporation. Well,
     the average earnings of the du Ponts for the period 1910 to 1914
     were $6,000,000 a year. It wasn't much, but the du Ponts managed
     to get along on it. Now let's look at their average yearly profit
     during the war years, 1914 to 1918. Fifty-eight million dollars a
     year profit we find! Nearly ten times that of normal times, and
     the profits of normal times were pretty good. An increase in
     profits of more than 950 per cent.

     Take one of our little steel companies that patriotically shunted
     aside the making of rails and girders and bridges to manufacture
     war materials. Well, their 1910-1914 yearly earnings averaged
     $6,000,000. Then came the war. And, like loyal citizens, Bethlehem
     Steel promptly turned to munitions making. Did their profits jump
     -- or did they let Uncle Sam in for a bargain? Well, their
     1914-1918 average was $49,000,000 a year!

     Or, let's take United States Steel. The normal earnings during the
     five-year period prior to the war were $105,000,000 a year. Not
     bad. Then along came the war and up went the profits. The average
     yearly profit for the period 1914-1918 was $240,000,000. Not bad.

     There you have some of the steel and powder earnings. Let's look
     at something else. A little copper, perhaps. That always does well
     in war times.

     Anaconda, for instance. Average yearly earnings during the pre-war
     years 1910-1914 of $10,000,000. During the war years 1914-1918
     profits leaped to $34,000,000 per year.

     Or Utah Copper. Average of $5,000,000 per year during the
     1910-1914 period. Jumped to an average of $21,000,000 yearly
     profits for the war period.

     Let's group these five, with three smaller companies. The total
     yearly average profits of the pre-war period 1910-1914 were
     $137,480,000. Then along came the war. The average yearly profits
     for this group skyrocketed to $408,300,000.

     A little increase in profits of approximately 200 per cent.

     Does war pay? It paid them. But they aren't the only ones. There
     are still others. Let's take leather.

     For the three-year period before the war the total profits of
     Central Leather Company were $3,500,000. That was approximately
     $1,167,000 a year. Well, in 1916 Central Leather returned a profit
     of $15,000,000, a small increase of 1,100 per cent. That's all.
     The General Chemical Company averaged a profit for the three years
     before the war of a little over $800,000 a year. Came the war, and
     the profits jumped to $12,000,000. a leap of 1,400 per cent.

     International Nickel Company -- and you can't have a war without
     nickel -- showed an increase in profits from a mere average of
     $4,000,000 a year to $73,000,000 yearly. Not bad? An increase of
     more than 1,700 per cent.

     American Sugar Refining Company averaged $2,000,000 a year for the
     three years before the war. In 1916 a profit of $6,000,000 was
     recorded.

     Listen to Senate Document No. 259. The Sixty-Fifth Congress,
     reporting on corporate earnings and government revenues.
     Considering the profits of 122 meat packers, 153 cotton
     manufacturers, 299 garment makers, 49 steel plants, and 340 coal
     producers during the war. Profits under 25 per cent were
     exceptional. For instance the coal companies made between 100 per
     cent and 7,856 per cent on their capital stock during the war. The
     Chicago packers doubled and tripled their earnings.

     And let us not forget the bankers who financed the great war. If
     anyone had the cream of the profits it was the bankers. Being
     partnerships rather than incorporated organizations, they do not
     have to report to stockholders. And their profits were as secret
     as they were immense. How the bankers made their millions and
     their billions I do not know, because those little secrets never
     become public -- even before a Senate investigatory body.

     But here's how some of the other patriotic industrialists and
     speculators chiseled their way into war profits.

     Take the shoe people. They like war. It brings business with
     abnormal profits. They made huge profits on sales abroad to our
     allies. Perhaps, like the munitions manufacturers and armament
     makers, they also sold to the enemy. For a dollar is a dollar
     whether it comes from Germany or from France. But they did well by
     Uncle Sam too. For instance, they sold Uncle Sam 35,000,000 pairs
     of hobnailed service shoes. There were 4,000,000 soldiers. Eight
     pairs, and more, to a soldier. My regiment during the war had only
     one pair to a soldier. Some of these shoes probably are still in
     existence. They were good shoes. But when the war was over Uncle
     Sam has a matter of 25,000,000 pairs left over. Bought -- and paid
     for. Profits recorded and pocketed.

     There was still lots of leather left. So the leather people sold
     your Uncle Sam hundreds of thousands of McClellan saddles for the
     cavalry. But there wasn't any American cavalry overseas! Somebody
     had to get rid of this leather, however. Somebody had to make a
     profit in it -- so we had a lot of McClellan saddles. And we
     probably have those yet.

     Also somebody had a lot of mosquito netting. They sold your Uncle
     Sam 20,000,000 mosquito nets for the use of the soldiers overseas.
     I suppose the boys were expected to put it over them as they tried
     to sleep in muddy trenches -- one hand scratching cooties on their
     backs and the other making passes at scurrying rats. Well, not one
     of these mosquito nets ever got to France!

     Anyhow, these thoughtful manufacturers wanted to make sure that no
     soldier would be without his mosquito net, so 40,000,000
     additional yards of mosquito netting were sold to Uncle Sam.

     There were pretty good profits in mosquito netting in those days,
     even if there were no mosquitoes in France. I suppose, if the war
     had lasted just a little longer, the enterprising mosquito netting
     manufacturers would have sold your Uncle Sam a couple of
     consignments of mosquitoes to plant in France so that more
     mosquito netting would be in order.

     Airplane and engine manufacturers felt they, too, should get their
     just profits out of this war. Why not? Everybody else was getting
     theirs. So $1,000,000,000 -- count them if you live long enough --
     was spent by Uncle Sam in building airplane engines that never
     left the ground! Not one plane, or motor, out of the billion
     dollars worth ordered, ever got into a battle in France. Just the
     same the manufacturers made their little profit of 30, 100, or
     perhaps 300 per cent.

     Undershirts for soldiers cost 14¢ [cents] to make and uncle Sam
     paid 30¢ to 40¢ each for them -- a nice little profit for the
     undershirt manufacturer. And the stocking manufacturer and the
     uniform manufacturers and the cap manufacturers and the steel
     helmet manufacturers -- all got theirs.

     Why, when the war was over some 4,000,000 sets of equipment --
     knapsacks and the things that go to fill them -- crammed
     warehouses on this side. Now they are being scrapped because the
     regulations have changed the contents. But the manufacturers
     collected their wartime profits on them -- and they will do it all
     over again the next time.

     There were lots of brilliant ideas for profit making during the
     war.

     One very versatile patriot sold Uncle Sam twelve dozen 48-inch
     wrenches. Oh, they were very nice wrenches. The only trouble was
     that there was only one nut ever made that was large enough for
     these wrenches. That is the one that holds the turbines at Niagara
     Falls. Well, after Uncle Sam had bought them and the manufacturer
     had pocketed the profit, the wrenches were put on freight cars and
     shunted all around the United States in an effort to find a use
     for them. When the Armistice was signed it was indeed a sad blow
     to the wrench manufacturer. He was just about to make some nuts to
     fit the wrenches. Then he planned to sell these, too, to your
     Uncle Sam.

     Still another had the brilliant idea that colonels shouldn't ride
     in automobiles, nor should they even ride on horseback. One has
     probably seen a picture of Andy Jackson riding in a buckboard.
     Well, some 6,000 buckboards were sold to Uncle Sam for the use of
     colonels! Not one of them was used. But the buckboard manufacturer
     got his war profit.

     The shipbuilders felt they should come in on some of it, too. They
     built a lot of ships that made a lot of profit. More than
     $3,000,000,000 worth. Some of the ships were all right. But
     $635,000,000 worth of them were made of wood and wouldn't float!
     The seams opened up -- and they sank. We paid for them, though.
     And somebody pocketed the profits.

     It has been estimated by statisticians and economists and
     researchers that the war cost your Uncle Sam $52,000,000,000. Of
     this sum, $39,000,000,000 was expended in the actual war itself.
     This expenditure yielded $16,000,000,000 in profits. That is how
     the 21,000 billionaires and millionaires got that way. This
     $16,000,000,000 profits is not to be sneezed at. It is quite a
     tidy sum. And it went to a very few.

     The Senate (Nye) committee probe of the munitions industry and its
     wartime profits, despite its sensational disclosures, hardly has
     scratched the surface.

     Even so, it has had some effect. The State Department has been
     studying "for some time" methods of keeping out of war. The War
     Department suddenly decides it has a wonderful plan to spring. The
     Administration names a committee -- with the War and Navy
     Departments ably represented under the chairmanship of a Wall
     Street speculator -- to limit profits in war time. To what extent
     isn't suggested. Hmmm. Possibly the profits of 300 and 600 and
     1,600 per cent of those who turned blood into gold in the World
     War would be limited to some smaller figure.

     Apparently, however, the plan does not call for any limitation of
     losses -- that is, the losses of those who fight the war. As far
     as I have been able to ascertain there is nothing in the scheme to
     limit a soldier to the loss of but one eye, or one arm, or to
     limit his wounds to one or two or three. Or to limit the loss of
     life.

     There is nothing in this scheme, apparently, that says not more
     than 12 per cent of a regiment shall be wounded in battle, or that
     not more than 7 per cent in a division shall be killed.

     Of course, the committee cannot be bothered with such trifling
     matters.




     CHAPTER THREE

     Who Pays The Bills?

     Who provides the profits -- these nice little profits of 20, 100,
     300, 1,500 and 1,800 per cent? We all pay them -- in taxation. We
     paid the bankers their profits when we bought Liberty Bonds at
     $100.00 and sold them back at $84 or $86 to the bankers. These
     bankers collected $100 plus. It was a simple manipulation. The
     bankers control the security marts. It was easy for them to
     depress the price of these bonds. Then all of us -- the people --
     got frightened and sold the bonds at $84 or $86. The bankers
     bought them. Then these same bankers stimulated a boom and
     government bonds went to par -- and above. Then the bankers
     collected their profits.

     But the soldier pays the biggest part of the bill.

     If you don't believe this, visit the American cemeteries on the
     battlefields abroad. Or visit any of the veteran's hospitals in
     the United States. On a tour of the country, in the midst of which
     I am at the time of this writing, I have visited eighteen
     government hospitals for veterans. In them are a total of about
     50,000 destroyed men -- men who were the pick of the nation
     eighteen years ago. The very able chief surgeon at the government
     hospital; at Milwaukee, where there are 3,800 of the living dead,
     told me that mortality among veterans is three times as great as
     among those who stayed at home.

     Boys with a normal viewpoint were taken out of the fields and
     offices and factories and classrooms and put into the ranks. There
     they were remolded; they were made over; they were made to "about
     face"; to regard murder as the order of the day. They were put
     shoulder to shoulder and, through mass psychology, they were
     entirely changed. We used them for a couple of years and trained
     them to think nothing at all of killing or of being killed.

     Then, suddenly, we discharged them and told them to make another
     "about face" ! This time they had to do their own readjustment,
     sans [without] mass psychology, sans officers' aid and advice and
     sans nation-wide propaganda. We didn't need them any more. So we
     scattered them about without any "three-minute" or "Liberty Loan"
     speeches or parades. Many, too many, of these fine young boys are
     eventually destroyed, mentally, because they could not make that
     final "about face" alone.

     In the government hospital in Marion, Indiana, 1,800 of these boys
     are in pens! Five hundred of them in a barracks with steel bars
     and wires all around outside the buildings and on the porches.
     These already have been mentally destroyed. These boys don't even
     look like human beings. Oh, the looks on their faces! Physically,
     they are in good shape; mentally, they are gone.

     There are thousands and thousands of these cases, and more and
     more are coming in all the time. The tremendous excitement of the
     war, the sudden cutting off of that excitement -- the young boys
     couldn't stand it.

     That's a part of the bill. So much for the dead -- they have paid
     their part of the war profits. So much for the mentally and
     physically wounded -- they are paying now their share of the war
     profits. But the others paid, too -- they paid with heartbreaks
     when they tore themselves away from their firesides and their
     families to don the uniform of Uncle Sam -- on which a profit had
     been made. They paid another part in the training camps where they
     were regimented and drilled while others took their jobs and their
     places in the lives of their communities. The paid for it in the
     trenches where they shot and were shot; where they were hungry for
     days at a time; where they slept in the mud and the cold and in
     the rain -- with the moans and shrieks of the dying for a horrible
     lullaby.

     But don't forget -- the soldier paid part of the dollars and cents
     bill too.

     Up to and including the Spanish-American War, we had a prize
     system, and soldiers and sailors fought for money. During the
     Civil War they were paid bonuses, in many instances, before they
     went into service. The government, or states, paid as high as
     $1,200 for an enlistment. In the Spanish-American War they gave
     prize money. When we captured any vessels, the soldiers all got
     their share -- at least, they were supposed to. Then it was found
     that we could reduce the cost of wars by taking all the prize
     money and keeping it, but conscripting [drafting] the soldier
     anyway. Then soldiers couldn't bargain for their labor, Everyone
     else could bargain, but the soldier couldn't.

     Napoleon once said,

          "All men are enamored of decorations . . . they
          positively hunger for them."

     So by developing the Napoleonic system -- the medal business --
     the government learned it could get soldiers for less money,
     because the boys liked to be decorated. Until the Civil War there
     were no medals. Then the Congressional Medal of Honor was handed
     out. It made enlistments easier. After the Civil War no new medals
     were issued until the Spanish-American War.

     In the World War, we used propaganda to make the boys accept
     conscription. They were made to feel ashamed if they didn't join
     the army.

     So vicious was this war propaganda that even God was brought into
     it. With few exceptions our clergymen joined in the clamor to
     kill, kill, kill. To kill the Germans. God is on our side . . . it
     is His will that the Germans be killed.

     And in Germany, the good pastors called upon the Germans to kill
     the allies . . . to please the same God. That was a part of the
     general propaganda, built up to make people war conscious and
     murder conscious.

     Beautiful ideals were painted for our boys who were sent out to
     die. This was the "war to end all wars." This was the "war to make
     the world safe for democracy." No one mentioned to them, as they
     marched away, that their going and their dying would mean huge war
     profits. No one told these American soldiers that they might be
     shot down by bullets made by their own brothers here. No one told
     them that the ships on which they were going to cross might be
     torpedoed by submarines built with United States patents. They
     were just told it was to be a "glorious adventure."

     Thus, having stuffed patriotism down their throats, it was decided
     to make them help pay for the war, too. So, we gave them the large
     salary of $30 a month.

     All they had to do for this munificent sum was to leave their dear
     ones behind, give up their jobs, lie in swampy trenches, eat
     canned willy (when they could get it) and kill and kill and kill .
     . . and be killed.

     But wait!

     Half of that wage (just a little more than a riveter in a shipyard
     or a laborer in a munitions factory safe at home made in a day)
     was promptly taken from him to support his dependents, so that
     they would not become a charge upon his community. Then we made
     him pay what amounted to accident insurance -- something the
     employer pays for in an enlightened state -- and that cost him $6
     a month. He had less than $9 a month left.

     Then, the most crowning insolence of all -- he was virtually
     blackjacked into paying for his own ammunition, clothing, and food
     by being made to buy Liberty Bonds. Most soldiers got no money at
     all on pay days.

     We made them buy Liberty Bonds at $100 and then we bought them
     back -- when they came back from the war and couldn't find work --
     at $84 and $86. And the soldiers bought about $2,000,000,000 worth
     of these bonds!

     Yes, the soldier pays the greater part of the bill. His family
     pays too. They pay it in the same heart-break that he does. As he
     suffers, they suffer. At nights, as he lay in the trenches and
     watched shrapnel burst about him, they lay home in their beds and
     tossed sleeplessly -- his father, his mother, his wife, his
     sisters, his brothers, his sons, and his daughters.

     When he returned home minus an eye, or minus a leg or with his
     mind broken, they suffered too -- as much as and even sometimes
     more than he. Yes, and they, too, contributed their dollars to the
     profits of the munitions makers and bankers and shipbuilders and
     the manufacturers and the speculators made. They, too, bought
     Liberty Bonds and contributed to the profit of the bankers after
     the Armistice in the hocus-pocus of manipulated Liberty Bond
     prices.

     And even now the families of the wounded men and of the mentally
     broken and those who never were able to readjust themselves are
     still suffering and still paying.




     CHAPTER FOUR

     How To Smash This Racket!

     WELL, it's a racket, all right.

     A few profit -- and the many pay. But there is a way to stop it.
     You can't end it by disarmament conferences. You can't eliminate
     it by peace parleys at Geneva. Well-meaning but impractical groups
     can't wipe it out by resolutions. It can be smashed effectively
     only by taking the profit out of war.

     The only way to smash this racket is to conscript capital and
     industry and labor before the nations manhood can be conscripted.
     One month before the Government can conscript the young men of the
     nation -- it must conscript capital and industry and labor. Let
     the officers and the directors and the high-powered executives of
     our armament factories and our munitions makers and our
     shipbuilders and our airplane builders and the manufacturers of
     all the other things that provide profit in war time as well as
     the bankers and the speculators, be conscripted -- to get $30 a
     month, the same wage as the lads in the trenches get.

     Let the workers in these plants get the same wages -- all the
     workers, all presidents, all executives, all directors, all
     managers, all bankers -- yes, and all generals and all admirals
     and all officers and all politicians and all government office
     holders -- everyone in the nation be restricted to a total monthly
     income not to exceed that paid to the soldier in the trenches!

     Let all these kings and tycoons and masters of business and all
     those workers in industry and all our senators and governors and
     majors pay half of their monthly $30 wage to their families and
     pay war risk insurance and buy Liberty Bonds.

     Why shouldn't they?

     They aren't running any risk of being killed or of having their
     bodies mangled or their minds shattered. They aren't sleeping in
     muddy trenches. They aren't hungry. The soldiers are!

     Give capital and industry and labor thirty days to think it over
     and you will find, by that time, there will be no war. That will
     smash the war racket -- that and nothing else.

     Maybe I am a little too optimistic. Capital still has some say. So
     capital won't permit the taking of the profit out of war until the
     people -- those who do the suffering and still pay the price --
     make up their minds that those they elect to office shall do their
     bidding, and not that of the profiteers.

     Another step necessary in this fight to smash the war racket is
     the limited plebiscite to determine whether a war should be
     declared. A plebiscite not of all the voters but merely of those
     who would be called upon to do the fighting and dying. There
     wouldn't be very much sense in having a 76-year-old president of a
     munitions factory or the flat-footed head of an international
     banking firm or the cross-eyed manager of a uniform manufacturing
     plant -- all of whom see visions of tremendous profits in the
     event of war -- voting on whether the nation should go to war or
     not. They never would be called upon to shoulder arms -- to sleep
     in a trench and to be shot. Only those who would be called upon to
     risk their lives for their country should have the privilege of
     voting to determine whether the nation should go to war.

     There is ample precedent for restricting the voting to those
     affected. Many of our states have restrictions on those permitted
     to vote. In most, it is necessary to be able to read and write
     before you may vote. In some, you must own property. It would be a
     simple matter each year for the men coming of military age to
     register in their communities as they did in the draft during the
     World War and be examined physically. Those who could pass and who
     would therefore be called upon to bear arms in the event of war
     would be eligible to vote in a limited plebiscite. They should be
     the ones to have the power to decide -- and not a Congress few of
     whose members are within the age limit and fewer still of whom are
     in physical condition to bear arms. Only those who must suffer
     should have the right to vote.

     A third step in this business of smashing the war racket is to
     make certain that our military forces are truly forces for defense
     only.

     At each session of Congress the question of further naval
     appropriations comes up. The swivel-chair admirals of Washington
     (and there are always a lot of them) are very adroit lobbyists.
     And they are smart. They don't shout that "We need a lot of
     battleships to war on this nation or that nation." Oh no. First of
     all, they let it be known that America is menaced by a great naval
     power. Almost any day, these admirals will tell you, the great
     fleet of this supposed enemy will strike suddenly and annihilate
     125,000,000 people. Just like that. Then they begin to cry for a
     larger navy. For what? To fight the enemy? Oh my, no. Oh, no. For
     defense purposes only.

     Then, incidentally, they announce maneuvers in the Pacific. For
     defense. Uh, huh.

     The Pacific is a great big ocean. We have a tremendous coastline
     on the Pacific. Will the maneuvers be off the coast, two or three
     hundred miles? Oh, no. The maneuvers will be two thousand, yes,
     perhaps even thirty-five hundred miles, off the coast.

     The Japanese, a proud people, of course will be pleased beyond
     expression to see the united States fleet so close to Nippon's
     shores. Even as pleased as would be the residents of California
     were they to dimly discern through the morning mist, the Japanese
     fleet playing at war games off Los Angeles.

     The ships of our navy, it can be seen, should be specifically
     limited, by law, to within 200 miles of our coastline. Had that
     been the law in 1898 the Maine would never have gone to Havana
     Harbor. She never would have been blown up. There would have been
     no war with Spain with its attendant loss of life. Two hundred
     miles is ample, in the opinion of experts, for defense purposes.
     Our nation cannot start an offensive war if its ships can't go
     further than 200 miles from the coastline. Planes might be
     permitted to go as far as 500 miles from the coast for purposes of
     reconnaissance. And the army should never leave the territorial
     limits of our nation.

     To summarize: Three steps must be taken to smash the war racket.

       1. We must take the profit out of war.

       2. We must permit the youth of the land who would bear arms to
          decide whether or not there should be war.

       3. We must limit our military forces to home defense purposes.




     CHAPTER FIVE

     To Hell With War!

     I am not a fool as to believe that war is a thing of the past. I
     know the people do not want war, but there is no use in saying we
     cannot be pushed into another war.

     Looking back, Woodrow Wilson was re-elected president in 1916 on a
     platform that he had "kept us out of war" and on the implied
     promise that he would "keep us out of war." Yet, five months later
     he asked Congress to declare war on Germany.

     In that five-month interval the people had not been asked whether
     they had changed their minds. The 4,000,000 young men who put on
     uniforms and marched or sailed away were not asked whether they
     wanted to go forth to suffer and die.

     Then what caused our government to change its mind so suddenly?

     Money.

     An allied commission, it may be recalled, came over shortly before
     the war declaration and called on the President. The President
     summoned a group of advisers. The head of the commission spoke.
     Stripped of its diplomatic language, this is what he told the
     President and his group:

          "There is no use kidding ourselves any longer. The cause
          of the allies is lost. We now owe you (American bankers,
          American munitions makers, American manufacturers,
          American speculators, American exporters) five or six
          billion dollars.

          If we lose (and without the help of the United States we
          must lose) we, England, France and Italy, cannot pay
          back this money . . . and Germany won't.

          So . . . "

     Had secrecy been outlawed as far as war negotiations were
     concerned, and had the press been invited to be present at that
     conference, or had radio been available to broadcast the
     proceedings, America never would have entered the World War. But
     this conference, like all war discussions, was shrouded in utmost
     secrecy. When our boys were sent off to war they were told it was
     a "war to make the world safe for democracy" and a "war to end all
     wars."

     Well, eighteen years after, the world has less of democracy than
     it had then. Besides, what business is it of ours whether Russia
     or Germany or England or France or Italy or Austria live under
     democracies or monarchies? Whether they are Fascists or
     Communists? Our problem is to preserve our own democracy.

     And very little, if anything, has been accomplished to assure us
     that the World War was really the war to end all wars.

     Yes, we have had disarmament conferences and limitations of arms
     conferences. They don't mean a thing. One has just failed; the
     results of another have been nullified. We send our professional
     soldiers and our sailors and our politicians and our diplomats to
     these conferences. And what happens?

     The professional soldiers and sailors don't want to disarm. No
     admiral wants to be without a ship. No general wants to be without
     a command. Both mean men without jobs. They are not for
     disarmament. They cannot be for limitations of arms. And at all
     these conferences, lurking in the background but all-powerful,
     just the same, are the sinister agents of those who profit by war.
     They see to it that these conferences do not disarm or seriously
     limit armaments.

     The chief aim of any power at any of these conferences has not
     been to achieve disarmament to prevent war but rather to get more
     armament for itself and less for any potential foe.

     There is only one way to disarm with any semblance of
     practicability. That is for all nations to get together and scrap
     every ship, every gun, every rifle, every tank, every war plane.
     Even this, if it were possible, would not be enough.

     The next war, according to experts, will be fought not with
     battleships, not by artillery, not with rifles and not with
     machine guns. It will be fought with deadly chemicals and gases.

     Secretly each nation is studying and perfecting newer and
     ghastlier means of annihilating its foes wholesale. Yes, ships
     will continue to be built, for the shipbuilders must make their
     profits. And guns still will be manufactured and powder and rifles
     will be made, for the munitions makers must make their huge
     profits. And the soldiers, of course, must wear uniforms, for the
     manufacturer must make their war profits too.

     But victory or defeat will be determined by the skill and
     ingenuity of our scientists.

     If we put them to work making poison gas and more and more
     fiendish mechanical and explosive instruments of destruction, they
     will have no time for the constructive job of building greater
     prosperity for all peoples. By putting them to this useful job, we
     can all make more money out of peace than we can out of war --
     even the munitions makers.

     So...I say,

     TO HELL WITH WAR!




       http://www.ratical.org/ratville/CAH/warisaracket.html (hypertext)
       http://www.ratical.org/ratville/CAH/warisaracket.txt  (text only)
       http://www.ratical.org/ratville/CAH/warisaracket.pdf (print ready)

I Declare WAR!

Happy Friday, dear readers!



The profanity was part of the FB posting, just so you understand. This is not going to turn into the Potty Mouth Picture Show.



Rehab facility has accepted me for treatment for the next two weeks -  it's a wonderful facility and now I have my laptop, so I can clean up the spelling errors within).



You'll note (only if you are part of my FB family) that I was on a bit of a tear for the last couple of days...and then I disappeared rather abruptly last night.



I embarked on a Candy Crush marathon; waiting for lives to be replenished at Level 28. Will go back to a couple of levels (now 37!).



So, I awaken this morning, and I put on the Ted Broer show. Ted and his family runs Healthmasters.com - this is an ultra high-end nutrition and wellness company. Ted is 62 and totally kick-ASS!



So imagine my surprise when the show begins, and it sounds as if they are reading my postings of the last couple of days live!!!



WOW!



What an affirmation that I am doing the right thing!!!



Here's the URL of the show in question: https://itunes.apple.com/us/podcast/the-ted-broer-show-mp3-edition/id1050535625?mt=2#episodeGuid=http%3A%2F%2Fmediaarchives.gsradio.net%2FTed_Broer%2F060216.mp3



Now, you could surmise that I'm utterly full of shite (one change I have made is using the actual invective instead of FCUK...people drop the F-bomb like girls drop a Beej - but that doesn't mean that a liberal use of the word 'shite' without the 'e' is warranted), but I have that posting archived and date stamped.



Anyone familiar with my work will actually gasp in astonishment - just imagine that the show you're hearing is the show as always performed by Ted and Austin Broer...but that the first fifteen minutes have been scripted by yours truly.



Here's some of that data:



Okay...are you ready for some information?


I currently write a blog regarding the dangers of GMOs,and while I haven't personally performed the experiments upon the FrankenFoods I strive to avoid, I can follow along on the research performed by the likes of Dr. Don Huber, Professor Stephanie Seneff​​, Anthony Samsel and others.


One of the methods used by their pesticides is chelation. Chelation works by binding with vitamins and nutrients so that organisms cannot absorb them.


(that means US, as well).
GMOs, simply by nature of this function, cannot possibly provide the same level of nutrition as conventional and/or organic crops.


There are a line of products that go by the designation BT, and they have been modified to create a toxin within their cells that explode the stomach of the insects that ingest them. Two problems with this:


1. Stomachs are stomachs. Why would one suppose that our stomachs aren't affected by the BT toxin? Traces have been found in human intestines;


2. These people cannot be serious scientists...how is it that one would go in and change the functionality of a cell, and yet not expect that some functionality not directly related to said function to be affected?


Lastly, adaptation. Flora and fauna adapt, or they die.


We now have superweeds and superbugs.


Thanks, Monsanto.


(this was typed on an iPhone with huge sausage-like fingers, so i hope you appreciate this.)



To the scumbags and utter MOTHERFUCKERS of our world - I just want you to know that you are now irrevocably and throroughly FUCKED...and I mean porn-style, all orifices, money shot FUCKED!



I will NEVER GIVE UP on making our world a better place.



NEVER.



So, FUCK OFF right now to a coffin, get in that bitch, close the lid and nail it shut from the inside, or, rest assured, I will be there to take a hammer to your rotten skulls, and a 2x4 to your holes.



I am not kidding, FUCKTARDS - the MOTHERFUCKING MAIN MAN HAS DECLARED ALL-OUT WAR ON SHITHEADS, SCUMBAGS AND UTTER DOUCHEBAGGERY.



Feel that spiked glove across your cheek...that's the love tap before the fisting...and I don't use lube.

Update:  Here's a great blog - It Is What It Is - Dr. Rex

Just a teaser:

Glyphosate, pathways to modern diseases II: Celiac sprue and gluten intolerance (Re-Post from NCBI)

Ted Broer of Healthmasters mention on his latest broadcast as to how glyphosate interferes with the small intestine, and I thought I should look it up:

Glyphosate, pathways to modern diseases II: Celiac sprue and gluten intolerance

Anthony Samsel¹ and Stephanie Seneff²

¹Independent Scientist and Consultant, Deerfield, NH 03037, USA

²Computer Science and Artificial Intelligence Laboratory, MIT, Cambridge, MA, USA

Corresponding author.

Correspondence address:Stephanie Seneff, PhD., Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Rm G-438 MIT Stata Center, 32 Vassar Street, Cambridge, MA 02139, USA. TEL.: +1-617-253-0451. FAX: +1-617-258-8642. E-MAIL: ude.tim.liasc@ffenes

Author information ► Article notes ► Copyright and License information ►

Received 2013 Sep 24; Revised 2013 Nov 10; Accepted 2013 Nov 12.

Copyright © 2013 Slovak Toxicology Society SETOX

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

This article has been cited by other articles in PMC.

Abstract

Celiac disease, and, more generally, gluten intolerance, is a growing problem worldwide, but especially in North America and Europe, where an estimated 5% of the population now suffers from it. Symptoms include nausea, diarrhea, skin rashes, macrocytic anemia and depression. It is a multifactorial disease associated with numerous nutritional deficiencies as well as reproductive issues and increased risk to thyroid disease, kidney failure and cancer. Here, we propose that glyphosate, the active ingredient in the herbicide, Roundup^®, is the most important causal factor in this epidemic. Fish exposed to glyphosate develop digestive problems that are reminiscent of celiac disease. Celiac disease is associated with imbalances in gut bacteria that can be fully explained by the known effects of glyphosate on gut bacteria. Characteristics of celiac disease point to impairment in many cytochrome P450 enzymes, which are involved with detoxifying environmental toxins, activating vitamin D3, catabolizing vitamin A, and maintaining bile acid production and sulfate supplies to the gut. Glyphosate is known to inhibit cytochrome P450 enzymes. Deficiencies in iron, cobalt, molybdenum, copper and other rare metals associated with celiac disease can be attributed to glyphosate's strong ability to chelate these elements. Deficiencies in tryptophan, tyrosine, methionine and selenomethionine associated with celiac disease match glyphosate's known depletion of these amino acids. Celiac disease patients have an increased risk to non-Hodgkin's lymphoma, which has also been implicated in glyphosate exposure. Reproductive issues associated with celiac disease, such as infertility, miscarriages, and birth defects, can also be explained by glyphosate. Glyphosate residues in wheat and other crops are likely increasing recently due to the growing practice of crop desiccation just prior to the harvest. We argue that the practice of “ripening” sugar cane with glyphosate may explain the recent surge in kidney failure among agricultural workers in Central America. We conclude with a plea to governments to reconsider policies regarding the safety of glyphosate residues in foods.

Keywords: celiac disease, gluten, glyphosate, food, cytochrome P450, deficiency

1 Introduction

Gluten intolerance is a growing epidemic in the U.S. and, increasingly, worldwide. Celiac sprue is a more specific disorder, characterized by gluten intolerance along with autoantibodies to the protein, transglutaminase, which builds crosslinks in undigested fragments of gliadin, a major constituent of gluten (Green & Cellier, 2007). The autoantibodies are produced as an immune response to undegraded fragments of proteins in gluten. A remarkable set of symptoms develop over time in association with celiac disease, including weight loss, diarrhea, chronic fatigue, neurological disorders, anemia, nausea, skin rashes, depression, and nutrient deficiencies. Usually, but not always, a strict gluten-free diet can alleviate many of the symptoms. A key associated pathology is an inflammatory response in the upper small intestine, leading to villous atrophy, a flattening of the microvilli which impairs their ability to function in their important role in absorbing nutrients.

Some have suggested that the recent surge in celiac disease is simply due to better diagnostic tools. However, a recent study tested frozen sera obtained between 1948 and 1954 for antibodies to gluten, and compared the results with sera obtained from a matched sample from people living today (Rubio-Topia et al., 2009). They identified a four-fold increase in the incidence of celiac disease in the newer cohort compared to the older one. They also determined that undiagnosed celiac disease is associated with a 4-fold increased risk of death, mostly due to increased cancer risk. They concluded that the prevalence of undiagnosed celiac disease has increased dramatically in the United States during the past 50 years.

Transglutaminases play many important roles in the body, as they form covalent crosslinks in complex proteins in connection with blood coagulation, skin-barrier formation, extracellular matrix assembly, and fertilization, endowing the substrate with protection from degradation by proteases (Lorand & Graham, 2003). They also form crosslinks in undigested fragments of gliadin derived from wheat, and sensitivity to certain of these fragments leads to the development of autoantibodies to tissue transglutaminase (Esposito et al., 2002) that inhibit its activity.

Glyphosate is the active ingredient in the herbicide Roundup. It is a broad-spectrum herbicide, considered to be nearly nontoxic to humans (Williams et al., 2000). However, a recent paper (Samsel & Seneff, 2013), argued that glyphosate may be a key contributor to the obesity epidemic and the autism epidemic in the United States, as well as to several other diseases and conditions, such as Alzheimer's disease, Parkinson's disease, infertility, depression, and cancer. Glyphosate suppresses 5-enolpyruvylshikimic acid-3-phosphate synthase (EPSP synthase), the rate-limiting step in the synthesis of the aromatic amino acids, tryptophan, tyrosine, and phenylalanine, in the shikimate pathway of bacteria, archaea and plants (de María et al., 1996). In plants, aromatic amino acids collectively represent up to 35% of the plant dry mass (Franz, 1997). This mode of action is unique to glyphosate among all emergent herbicides. Humans do not possess this pathway, and therefore we depend upon our ingested food and our gut microbes to provide these essential nutrients. Glyphosate, patented as an antimicrobial (Monsanto Technology LLC, 2010), has been shown to disrupt gut bacteria in animals, preferentially killing beneficial forms and causing an overgrowth of pathogens. Two other properties of glyphosate also negatively impact human health – chelation of minerals such as iron and cobalt, and interference with cytochrome P450 (CYP) enzymes, which play many important roles in the body. We will have much more to say about these aspects in later sections of this paper.

A recent study on glyphosate exposure in carnivorous fish revealed remarkable adverse effects throughout the digestive system (Senapati et al., 2009). The activity of protease, lipase, and amylase were all decreased in the esophagus, stomach, and intestine of these fish following exposure to glyphosate. The authors also observed “disruption of mucosal folds and disarray of microvilli structure” in the intestinal wall, along with an exaggerated secretion of mucin throughout the alimentary tract. These features are highly reminiscent of celiac disease. Gluten peptides in wheat are hydrophobic and therefore resistant to degradation by gastric, pancreatic and intestinal proteases (Hershko & Patz, 2008). Thus, the evidence from this effect on fish suggests that glyphosate may interfere with the breakdown of complex proteins in the human stomach, leaving larger fragments of wheat in the human gut that will then trigger an autoimmune response, leading to the defects in the lining of the small intestine that are characteristic of these fish exposed to glyphosate and of celiac patients. As illustrated in Figure 1, the usage of glyphosate on wheat in the U.S. has risen sharply in the last decade, in step with the sharp rise in the incidence of Celiac disease. We explain the reasons for increased application of glyphosate to wheat in Section 13.

Figure 1

Hospital discharge diagnosis (any) of celiac disease ICD-9 579 and glyphosate applications to wheat (R=0.9759, p≤1.862e-06). Sources: USDA:NASS; CDC. (Figure courtesy of Nancy Swanson).

In the remainder of this paper, we will first show that gut dysbiosis, brought on by exposure to glyphosate, plays a crucial role in the development of celiac disease. Many CYP enzymes are impaired in association with celiac disease, and we show that glyphosate's known suppression of CYP enzyme activity in plants and animals plausibly explains this effect in humans. In Section 4, we describe the role of excess retinoic acid in celiac disease, and show how this ties also to reproductive problems. We link this to the known effects of glyphosate on retinoic acid, mediated by its suppression of CYP enzymes. Section 5 addresses cobalamin deficiency, a known pathology associated with celiac disease that leads to macrocytic anemia. We argue that this follows as a direct consequence of glyphosate's ability to chelate cobalt. Section 6 discusses in more depth the role of anemia in celiac disease, a consequence of both cobalamin and iron deficiency. Section 7 discusses molybdenum deficiency and its link to microcephaly, which is associated with celiac disease. Section 8 discusses the link between selenium deficiency and autoimmune thyroid disease. Section 9 discusses kidney disease in connection with celiac disease and glyphosate. Section 10 discusses various nutritional deficiencies associated with celiac disease, and shows how these can directly be explained by glyphosate. Section 11 discusses the link between celiac disease and certain rare cancers that have also been linked to glyphosate. Section 12 goes into an in-depth discussion of how glyphosate might promote autoantibodies to transglutaminase. Following a section which presents compelling evidence that glyphosate residues in wheat, sugar and other crops are likely increasing in recent decades, and a section discussing the increased risk to kidney failure in agricultural workers exposed to excess glyphosate occupationally, we close with a discussion section that summarizes our findings, and a conclusion which implores governments to pay more attention to the damaging consequences of the escalation in chemical warfare on weeds that characterizes current agricultural practices.

2 Gut bacteria

In this section, we first discuss the role of pathogens in inducing the breakdown of tight junctions in enterocytes lining the small intestinal wall. We then show that glyphosate is associated with an overgrowth of pathogens along with an inflammatory bowel disease in animal models. A parallel exists with celiac disease where the bacteria that are positively and negatively affected by glyphosate are overgrown or underrepresented respectively in association with celiac disease in humans. We also discuss how the beneficial bacteria that are negatively impacted by glyphosate can protect from celiac disease through their enzymatic activities on gluten, and point to several articles recommending treatment plans based on probiotics.

Pathogens, through their activation of a potent signaling molecule called zonulin, induce a breakdown of the tight junctions in cells lining the gut, leading to “leaky gut” syndrome (Fasano, 2011). Concentrations of zonulin were sharply elevated (p<0.000001) in subjects with celiac disease during the acute phase (Fasano et al., 2000). As many as 30% of celiac patients continue to experience GI symptoms after adopting a gluten-free diet, despite optimal adherence, a condition that was attributed to bacterial overgrowth in the small intestine (Tursi et al., 2003). Figure 2 shows that there is a correlation between glyphosate application to wheat and the incidence of intestinal infections.

Figure 2

Deaths due to intestinal infections ICD A04, A09; 008, 009 with glyphosate applications to wheat (R=0.9834, p≤3.975e-09). Sources: USDA:NASS; CDC. (Figure courtesy of Nancy Swanson).

Evidence of disruption of gut bacteria by glyphosate is available for poultry (Shehata et al., 2013), cattle (Krüger et al., 2013), and swine (Carman et al., 2013). Glyphosate disrupts the balance of gut bacteria in poultry (Shehata et al., 2013), increasing the ratio of pathogenic bacteria to other commensal microbes. Salmonella and Clostridium are highly resistant to glyphosate, whereas Enterococcus, Bifidobacteria, and Lactobacillus are especially susceptible. Glyphosate was proposed as a possible factor in the increased risk to Clostridium botulinum infection in cattle in Germany over the past ten to fifteen years (Krüger et al., 2013b). Pigs fed GMO corn and soy developed widespread intestinal inflammation that may have been due in part to glyphosate exposure (Carman et al., 2013).

Celiac disease is associated with reduced levels of Enterococcus, Bifidobacteria and Lactobacillus in the gut and an overgrowth of pathogenic gram negative bacteria (Sanz et al., 2011; Di Cagno et al., 2011; Collado et al., 2007). In (Di Cagno et al., 2011), Lactobacillus, Enterococcus and Bifidobacteria were found to be significantly lower in fecal samples of children with celiac disease compared to controls, while levels of the pathogens, Bacteroides, Staphylococcus, Salmonella, a Shighella were elevated. In (Collado et al., 2007), another study comparing the fecal material of celiac infants to healthy controls, Bacteroides, Clostridium and Staphylococcus were all found to be significantly higher (p<0.05). Sulfate-reducing bacterial counts were also elevated (p<0.05) (Nadal et al., 2007; Collado et al., 2007), an interesting observation which we will return to later in this paper. A significant reduction in Bifidobacteria was also found in (Nadal et al., 2007). An increased excretion of the bacterial metabolites p-Cresol and phenol has also been recognized in association with celiac disease (Tamm, 1984). p-Cresol is produced via anaerobic metabolism of tyrosine by pathogenic bacteria such as Clostridium difficile (D'Ari and Barker, 1985). It is a highly toxic carcinogen, which also causes adverse effects on the central nervous system, the cardiovascular system, lungs, kidney and liver (Kelly et al., 1994).

Probiotic treatments are recommended to aid in digestive healing in celiac disease. The proteolytic activity of Lactobacilli aids the breakdown of wheat into less allergenic forms. Ongoing research aims to produce gluten-containing sourdough breads fermented by Lactobacilli that can then serve as probiotics to help ameliorate the symptoms of celiac disease and allow celiac patients to consume wheat (Gobbetti et al., 2007). Probiotic Lactobacilli produce the enzyme phytase which breaks down phytates that would otherwise deplete important minerals and other cations through chelation (Famularo et al., 2005). Their activities would therefore improve absorption of these micronutrients, a known problem in celiac patients (Cavallaro et al., 2004). Glyphosate itself also chelates rare minerals, a subject we will address in the section on nutritional deficiencies.

Probiotic treatment with Bifidobacteria has been shown to alleviate symptoms associated with celiac disease (Smecuol et al., 2013; Whorwell et al., 2006). Bifidobacteria suppress the pro-inflammatory milieu triggered by the microbiota of celiac patients (Medina et al., 2008). Live cultures of Bifidobacterium lactis would promote healing of the gut if offered as treatment in conjunction with the gluten-free diet, or might even allow the celiac patient to consume modest amounts of gluten without damaging effects (Lindfors et al., 2008). In this in vitro study, it was demonstrated that B. lactis reduced epithelial permeability and improved the integrity of the tight junctions in human colon cells.

In summary, celiac disease is associated with a reduced presence in the gut of commensal bacteria such as Lactobacilli and Bifidobacteria, which are known to be preferentially killed by glyphosate, and with an overabundance of C. difficile, which is known to be promoted by glyphosate exposure. Bifidobacteria and Lactobacilli are both capable of modifying gluten in such a way as to make it less allergenic, a feature that is being exploited in recent efforts to develop gluten-containing foods that may be safe for consumption by celiac patients. Probiotics containing live forms of these bacteria are also being actively marketed today.

3 CYP Enzyme impairment and sulfate depletion

As mentioned previously, glyphosate has been shown to suppress CYP enzymes in plants (Lamb et al., 1998) and animals (Hietanen et al., 1983). A study on rats demonstrated that glyphosate decreased the levels of CYP enzymes and monooxygenase activities in the liver and the intestinal activity of aryl hydrocarbon hydroxylase (Hietanen et al., 1983).

CYP enzymes are essential for detoxification of many compounds in the liver (Lindros, 1997). Intraperitoneal exposure of rats to Roundup in acute doses over a short time interval induced irreversible damage to hepatocytes and elevated urinary markers of kidney disease. This was associated with lipid peroxidation and elevated levels of the inflammatory cytokine tumor necrosis factor (TNF-α) (El-Shenawy, 2009). CYP3A is constitutively expressed in human intestinal villi and plays an important role in drug metabolism (Cupp & Tracy, 1998). Celiac disease is associated with a decrease in the intestinal CYP3A (Lang et al., 1996). This defect is restored by a gluten free diet.

Impaired gallbladder bile acid production (Colombato et al., 1977) and biliary cirrhosis, an inflammatory liver disease characterized by obstruction of the bile duct (Dickey et al., 1997), have been shown to co-occur with celiac disease. CYP enzymes are crucial in the production of bile acids (Lorbek et al., 2012). An obligatory CYP enzyme in bile acid synthesis, CYP27A, has been identified as being identical to the mitochondrial vitamin D3 activating enzyme (Wikvall, 2001). In (Kemppainen et al., 1999), 64% of men and 71% of women with celiac disease were found to be vitamin D3 deficient, manifested as low spinal bone mineral density. Celiac disease is associated with impaired gall bladder function and decreased pancreatic secretions (Brown et al., 1987; Benini et al., 2012) along with recurrent pancreatitis (Patel et al., 1999). Abnormalities in bile acid secretion have been found in children suffering from celiac disease (Ejderhamn et al., 1992). Celiac patients exhibit abnormally low synthesis of cholecystokinin (Deprez et al., 2002), but it has also become apparent that the gall bladder is less responsive to stimulation of contraction by cholecystokinin (Brown et al., 1987). A reversible defect of gallbladder emptying and cholecystokinin release has been identified in association with celiac disease (Maton et al., 1985). These pathologies may be related to impaired CYP enzyme activity induced by glyphosate.

While it is clear that CYP enzymes play an important role in bile acid synthesis and in cholesterol homeostasis, the details have not yet been worked out (Lorbek et al., 2012). However, some mouse knockout experiments produce embryonically lethal effects, pointing to the importance of these enzymes to biological systems. Disruption of Cyp7A1, involved in bile acid synthesis in mice, induces elevated serum cholesterol and early death.

A link has been established between celiac disease and non-alcoholic fatty liver, which is likely due to the liver's inability to export cholesterol sulfate through the bile acids due to impaired CYP enzymes (Lorbek et al., 2012). This requires a private store of fats to house the excess cholesterol that cannot be exported in bile. This would also likely lead to insufficient sulfate supplies to the small intestine, and could result in impaired heparan sulfate synthesis in the glycosaminoglycans and subsequent pathologies. Heparan sulfate populating the glycosaminoglycans (GAGs) surrounding enterocytes is essential for the proper functioning of the small intestines. Leakage of both albumin and water in both the vasculature and tissues results when the negative charge is reduced due to insufficient sulfation of the polysaccharide units (Sunergren et al., 1987). Vascular leakage may be a consequence of degradation of sulfated GAGs due to inflammatory agents (Klein et al., 1992). A similar problem may occur in the kidneys leading to albumin loss into urine during nephrosis (Vernier et al., 1983). Intestinal protein loss in inflammatory enteropathy associated with celiac disease may also be due to a deficiency in the sulfated GAGs (Murch et al., 1993; Murch, 1995). A case study of three infants with congenital absence of enterocyte heparan sulfate demonstrated profound enteric protein loss with secretory diarrhoea and absorption failure, even though their intestines were not inflamed (Murch et al., 1996).

In (Samsel and Seneff, 2013), a hypothesis was developed that glyphosate disrupts the transport of sulfate from the gut to the liver and pancreas, due to its competition as a similarly kosmotropic solute that also increases blood viscosity. (Kosmotropes are ions that induce “structure ordering” and “salting out” of suspended particles in colloids). Insufficient sulfate supply to the liver is a simple explanation for reduced bile acid production. The problem is compounded by impaired CYP enzymatic action and impaired cycling of bile acids through defective enterocytes in the upper small intestine. The catastrophic effect of loss of bile acids to the feces due to impaired reuptake compels the liver to adopt a conservative approach of significantly reduced bile acid synthesis, which, in turn, leads to gall bladder disease.

The protein, Nuclear factor κ-lightchain-enhancer of activated B cells (NF-κB) controls DNA transcription of hundreds of genes and is a key regulator of the immune response to infection (Tieri et al., 2012). Light chains are polypeptide subunits of immunoglobulins. NF-κB responds to stimulation from bacterial and viral antigens, inflammatory cytokines like TNF-α, free radicals, oxidized LDL, DNA damage and UV light. The incidence of acute pancreatitis has been increasing in recent years (Bhatia, 2012), and it often follows billiary disease. A local inflammatory reaction at the site of injury coincides with an increase in the synthesis of hydrogen sulfide (H₂S) gas. H₂S regulates the inflammatory response by exciting the extracellular signal regulated (ERK) pathway, leading to production of NF-κB (Bhatia, 2012). We hypothesize that H₂S, while toxic, is a source of both energy and sulfate for the pancreas, derived from sulfur-containing amino acids such as cysteine and homocysteine. Dehydroepiandrosterone (DHEA) sulfate, but not DHEA, inhibits NF-κB synthesis, suggesting that sulfate deficiency is a driver of inflammation (Iwasaki et al., 2004).

While H₂S is well known as a toxic gas through its inhibition of aerobic respiration, a recent paradigm shift in the research surrounding H₂S has been inspired by the realization that it is an important signaling gas in the vasculature, on par with nitric oxide (Li et al., 2011). H₂S can serve as an inorganic source of energy to mammalian cells (Módis et al., 2013). 3-mercaptopyruvate sulfurtransferae (3MST) is expressed in the vascular endothelium, and it produces H₂S from mercaptopyruvate, an intermediary in the breakdown of cysteine (Kimura, 2011). Endogenously produced H₂S derived from 3-mercaptopyruvate stimulates additional mitochondrial H₂S production, which then is oxidized to thiosulfate via at least three different pathways (Ingenbleek and Kimura, 2013; Hildebrandt and Grieshaber, 2008; Goubern et al., 2007), producing ATP. The inflammatory agent superoxide can act as substrate for the oxidation of H₂S to sulfite and subsequently sulfate and the activated form, PAPS (Seneff et al., 2012), but will likely induce oxidative damage in the pancreas, particularly, as we will see in section 7, if molybdenum deficiency impairs sulfite-to-sulfate synthesis.

Pancreatic beta cells express extraordinarily high levels of heparan sulfate, which is essential for their survival (Ziolkowski et al., 2012), since it protects them from ROS-induced cell death. Because sulfate transport via the hepatic portal vein is likely disrupted by glyphosate, H₂S, whether derived from sulfur-containing amino acids or supplied via diffusion following its production by sulfur-reducing bacteria in the gut, can become an important source of sulfur for subsequent sulfate production locally in the pancreatic cells. Pancreatic elastase is a serine protease that is needed to assist in protein degradation, but an overabundance can lead to autolysis of tissues (Ito et al., 1998). Cholesterol sulfate inhibits pancreatic elastase (Ito et al., 1998), so a deficiency in cholesterol sulfate supply due to impaired sulfate supply to the liver and impaired CYP function should increase the risk of tissue digestion by pancreatic enzymes, contributing to the loss of villi in the upper small intestine observed in celiac disease.

In the early 1990's a newly recognized disease began to appear, characterized by eosinophil infiltration into the esophagus, which manifested as dysphagia in adults and refractory reflux symptoms in children (Lucendo & Sánchez-Cazalilla, 2012). This disease, termed eosinophilic esophagitis (EOE), is associated with a Th2 immune profile and synthesis of the cytokine IL-13, which has direct cytotoxic effects on epithelial cells. A dose-dependent induction of eosinophilia by intratracheal delivery of IL-13 confirms its association with EOE (Mishra and Rothenberg, 2003). An association has been found between EOE and celiac disease (Leslie et al., 2010). Patients with refractory celiac disease that is not corrected by dietary gluten restriction show an increased production of IL-13 in the gut (Gross et al., 2013). The incidence of EOE has increased at alarming rates in Western countries in the last three decades (Furuta et al., 2007; Liacouras et al., 2011; Prasad et al., 2009).

Glyphosate is highly corrosive to the esophageal epidermal lining, with upper GI tract injury observed in 94% of patients following glyphosate ingestion (Chang et al., 1999). In (Zouaoui et al., 2013), the most common symptoms in an acute response from glyphosate poisoning were oropharyngeal ulceration, nausea and vomiting. We hypothesize that glyphosate induces EOE via a systemic response as well as through direct contact. The pathogenesis of EOE is related to food sensitivities, but airborne exposure to chemicals in the lungs can also induce it, so it does not require physical contact to the allergen (Blanchard & Rothenberg, 2008). It is conceivable that glyphosate is responsible for the emergence of EOE.

The cytochrome P450 reductase (CPR) and cytochrome P450 (CP) enzyme system is essential for inducing nitric oxide release from organic nitrates (Li, 2006). The nitrate moiety is reduced while simultaneously oxidizing NADPH to NADP+. This system is invoked in organic nitrate drug treatment for cardiovascular therapy. The reaction depends on anaerobic, acidic conditions, a feature of venous rather than arterial blood. Since L-arginine is substrate for NO synthesis by endothelial nitric oxide synthase (eNOS) under oxidative conditions (Förstermann and Münze, 2006), it is likely that CPR and CP play an important role mainly in stimulating venous smooth muscle relaxation. Impaired venous relaxation would likely contribute to venous thrombosis, which is a well-established complication of celiac disease (Zenjari et al., 1995; Marteau et al., 1994, Grigg, 1999, Halfdanarson et al., 2007).

In summary, celiac disease is associated with multiple pathologies in the digestive system, including impaired gall bladder function, fatty liver, pancreatitis, and EOE. We have argued here that many of these problems can be traced to impaired CYP function in the liver due to glyphosate exposure, leading to insufficient flow of bile acids through the circular pathway between the liver and the gut. This results in a system-wide depletion in sulfate, which induces inflammation in multiple organs to produce sulfate locally. A potential sulfur source for sulfate synthesis could be hydrogen sulfide gas, provided in part by the local breakdown of sulfur-containing amino acids like cysteine and homocysteine and in part by diffusion of the gas produced from inorganic dietary sources by sulfur-reducing bacteria in the large intestine. Impaired CYP enzyme function may also contribute to venous thrombosis, for which celiac disease is an established risk factor.

4 Retinoic acid, celiac disease and reproductive issues

In this section, we first establish that excess retinoic acid (RA) is a risk factor for celiac disease. We then show that excess RA leads to complications in pregnancy and teratogenic effects in offspring. Glyphosate has been shown to exhibit teratogenic effects in line with known consequences of excess RA exposure to the embryo, and we propose that the mechanism for this effect may be glyphosate's known disruption of CYP enzymes (Samsel & Seneff, 2013), which are involved in RA catabolism. This then links glyphosate to increased risk to celiac disease via its direct effects on RA. And it identifies a possibly important factor in the association of celiac disease with reproductive issues. We also discuss other adverse effects of excess retinoic acid and a possible relationship to impaired sulfate supply to the gut.

In celiac disease, T cells develop antibody responses against dietary gluten, a protein present in wheat (Jabri & Sollid, 2009). RA, a metabolite of vitamin A, has been shown to play a critical role in the induction of intestinal regulatory responses (Mora et al., 2008; Coombes et al., 2007; Mucida et al., 2007). The peptide in gluten, A-gliadin p31-43, induces interleukin 15 (IL-15), a key cytokine promoting T-cell activation (Hershko & Patz, 2008). RA synergizes with high levels of IL-15 to promote JNK phosphorylation (Nanda, 2011; DePaolo et al., 2011), which potentiates cellular apoptosis (Putcha et al., 2003). IL-15 is a causative factor driving the differentiation of precursor cells into anti-gluten CD4+ and CD8+ Th1 cells in the intestinal mucosa. Furthermore, in (DePaolo et al., 2011), it was discovered that RA exhibits an unanticipated co-adjuvant property to induce Th1 immunity to antigens during infection of the intestinal mucosa with pathogens. Retinoic acid has also been shown to directly suppress transglutaminase activity, another way in which it would negatively impact celiac disease (Thacher et al., 1985). Thus, it is becoming clear that excess exposure to RA would increase risk to celiac disease, and warnings have been issued regarding potential adverse effects of RA supplements on celiac disease.

It is well established that high RA levels leads to teratogenic effects both in human and experimental models. Brain abnormalities such as microcephaly, impairment of hindbrain development, mandibular and midfacial underdevelopment, and cleft palate are all implicated (Sulik et al., 1988; Clotman et al., 1998). Women with celiac disease are known to have higher rates of infertility, miscarriages, and birth defects in their offspring (Freeman, 2010; Martinelli et al., 2000; Dickey et al., 1996; Collin et al., 1996). Excess RA could be a significant factor in these complications.

A possible mechanism by which glyphosate might induce excess RA is via its interference with the CYP enzymes that metabolize RA. There are at least three known CYPs (CYP26A1, CYP26B1 and CYP26C1) that catabolize RA, and they are active in both the embryo and the adult (Taimi et al., 2004). A 1/5000 dilution of glyphosate was sufficient to induce reproducible malformations characteristic of RA exposure in frog embryos (Paganelli et al., 2010). Pathologies included shortening of the trunk, reduction in the size of the head, abnormally small eyes or the presence of only one eye (cyclopia), and other craniofacial malformations in the tadpole. Glyphosate's toxicity to tadpoles has been well demonstrated, as it killed nearly 100% of larval amphibians exposed in experimental outdoor pond mesocosms (Relyea, 2005).

According to official records, there has been a recent 4-fold increase in developmental malformations in the province of Chaco, Argentina, where glyphosate is used massively on GMO monocrops of soybeans (Carrasco, 2013). In Paraguay, 52 cases of malformations were reported in the offspring of women exposed during pregnancy to agrochemicals, including anencephaly, microcephaly, facial defects, cleft palate, ear malformations, polydactily, and syndactily (Benítez-Leite et al., 2009). In in vitro studies on human cell lines, DNA strand breaks, plasma membrane damage and apoptosis were observed following exposure to glyphosate-based herbicides (Gasnier et al., 2009). Another factor in teratogenetic effects of glyphosate may be the suppression of the activity of androgen-to-estrogen conversion by aromatase, a CYP enzyme (Gasnier et al., 2009).

Ingested vitamin A, a fat-soluble vitamin, is delivered to the blood via the lymph system in chylomicrons, and excess vitamin A is taken up by the liver as retinoic acid for catabolism by CYP enzymes (Russell, 2000). Any remaining retinoic acid that is not catabolized is exported inside LDL particles, and it lingers much longer as retinyl esters in the vasculature in this form (Krasinski et al., 1990). Excess retinoic acid is more readily stored in this way in LDL particles in the elderly. Vitamin A toxicity can lead to fatty liver and liver fibrosis (Russell, 2000) as well as hypertriglyceridemia (Ellis et al., 1986). Vitamin A has a negative effect on cholesterol sulfate synthesis (Jetten et al., 1989), which might negatively impact the liver's ability to maintain adequate supplies of cholesterol sulfate for the bile acids, and therefore also interfere with the supply of cholesterol sulfate to the gastrointestinal tract.

In summary, glyphosate's disruption of the CYP enzymes responsible for RA catabolism could lead to an excess bioavailability of RA that could contribute adversely to celiac disease, as well as damaging the liver and leading to teratogenic effects in offspring of exposed individuals.

In addition to higher risk to birth defects, individuals with celiac disease have increased risk to infertility (Meloni et al., 1999; Farthing et al., 1982). Increased incidence of hypogonadism, infertility and impotence was observed in a study of 28 males with celiac disease (Farthing et al., 1982). Marked abnormalities of sperm morphology and motility were noted, and endocrine dysfunction was suggested as a probable cause. In studies conducted on Sertoli cells in prepubertal rat testis, exposure to Roundup induced oxidative stress leading to cell death (de Liz Oliveira Cavalli et al., 2013). Roundup induced the opening of L-type voltage dependent calcium channels as well as ryanodine receptors, initiating ER stress and leading to calcium overload and subsequent necrosis. Glutathione was depleted due to upregulation of several glutathione-metabolizing enzymes. This suggests that Roundup would interfere with spermatogenesis, which would impair male fertility.

5 Cobalamin deficiency

Untreated celiac disease patients often have elevated levels of homocysteine, associated with folate and/or cobalamin deficiency (Saibeni et al., 2005; Dickey et al., 2008). Species of Lactobacillus and Bifidobacterium have the capability to biosynthesize folate (Rossi et al., 2011), so their disruption by glyphosate could contribute to folate deficiency. Malabsorption in the proximal small intestine could also lead to iron and folate deficiencies. Cobalamin was originally thought to be relatively spared in celiac disease because its absorption is mostly through the terminal ileum, which is unaffected by celiac disease. However, a recent study found that cobalamin deficiency is prevalent in celiac patients. 41% of the patients studied were found to be deficient in cobalamin (<220 ng/L), and 31% of these cobalamin-deficient patients also had folate deficiency (Dahele & Ghosh, 2001). Either cobalamin or folate deficiency leads directly to impaired methionine synthesis from homocysteine, because these two vitamins are both required for the reaction to take place. This induces hyperhomocysteinemia (Refsum et al., 2001), an established risk factor in association with celiac disease (Hadithi et al., 2009). Long-term cobalamin deficiency also leads to neurodegenerative diseases (Herrmann & Obeid, 2012).

Because a deficiency in cobalamin can generate a large pool of methyl-tetrahydrofolate that is unable to undergo reactions, cobalamin deficiency will often mimic folate deficiency. Cobalamin requires cobalt, centered within its corrin ring, to function. We depend upon our gut bacteria to produce cobalamin, and impaired cobalt supply would obviously lead to reduced synthesis of this critical molecule. Glyphosate is known to chelate +2 cations such as cobalt. Glyphosate complexes with cobalt as a dimer [Co(glyphosate)2]3 in fifteen different stereoisomeric configurations, and it is facile at switching among the different stereoisomers, an unusual kinetic property compared to most Co(III) systems (Cusiel, 2005).

In fact, studies have revealed that glyphosate inhibits other cytosolic enzymes besides EPSP synthase in plants and microbes that also activate steps in the shikimate pathway (Ganson and Jensen, 1988; Bode et al., 1984). Glyphosate potently inhibits three enzymes in the shikimate pathway in yeast (Bode et al., 1984). It has been confirmed that these other enzymes depend upon cobalt as a catalyst, and glyphosate inhibition works through competitive cobalt binding and interference with cobalt supply (Ganson and Jensen, 1988). It has also been proposed that chelation by glyphosate of both cobalt and magnesium contributes to impaired synthesis of aromatic amino acids in Escherichia coli bacteria (Hoagland and Duke, 1982). Thus, it is plausible that glyphosate similarly impairs cobalamin function in humans by chelating cobalt.

6 Anemia and iron

Anemia is one of the most common manifestations of celiac disease outside of the intestinal malabsorption issues (Halfdanarson et al., 2007; Bottaro et al., 1999), and is present in up to half of diagnosed celiac patients. Celiac patients often have both cobalamin and folate deficiency, which can cause anemia, but iron deficiency may be the most important factor (Hershko & Patz, 2008). Celiac patients often don't respond well to iron treatment.

Glyphosate's chelating action can have profound effects on iron in plants (Eker et al., 2006; Bellaloui et al., 2009). Glyphosate interferes with iron assimilation in both glyphosate-resistant and glyphosate-sensitive soybean crops (Bellaloui et al., 2009). It is therefore conceivable that glyphosate's chelation of iron is responsible for the refractory iron deficiency present in celiac disease.

Erythropoietin (EPO), also called hematopoietin, is a cytokine produced by interstitial fibroblasts in the kidney that regulates red blood cell production. Low EPO levels, leading to a low turnover rate of red blood cells, is a feature of celiac disease (Bergamaschi et al., 2008; Hershko & Patz, 2008). This can lead to megaloblastic anemia, where red blood cells are large (macrocytic) and reduced in number due to impaired DNA synthesis. A recent hematological study on mice exposed to Roundup at subacute levels for just 15 days revealed an anemic syndrome in both male and female mice, with a significant reduction in the number of erythrocytes and in hemoglobin, reduced hematocrit and increased mean corpuscular volume, indicative of macrocytic anemia (Jasper et al., 2012).

7 Molybdenum deficiency

Molybdenum deficiency is rarely considered in diagnoses, as it is only needed in trace amounts. However, molybdenum is essential for at least two very important enzymes: sulfite oxidase and xanthine oxidase. Sulfite oxidase converts sulfite, a highly reactive anion, to sulfate, which is much more stable. Sulfite is often present in foods such as wine and dried fruits as a preservative. Sulfate plays an essential role in the sulfated proteoglycans that populate the extracellular matrices of nearly all cell types (Turnbull et al., 2001; Murch et al., 1993; Murch, 1995). So, impaired sulfite oxidase activity leads to both oxidative damage and impaired sulfate supplies to the tissues, such as the enterocytes in the small intestine. The excess presence of sulfur-reducing bacteria such as Desulfovibrio in the gut in association with celiac disease (Collado et al., 2007; Nadal et al., 2007) could be protective, because these bacteria can reduce dietary sulfite to hydrogen sulfide, a highly diffusable gas that can migrate through tissues to provide a source of sulfur for sulfate regeneration at a distant site, as previously discussed. These distal sites could reoxidize the H₂S through an alternative pathway that does not require molybdenum for sulfur oxidation (Ingenbleek and Kimura, 2013).

Xanthine oxidase (XO) produces uric acid from xanthine and hypoxanthine, which are derived from purines. It is activated by iron, which, as we have seen, is often intractably deficient in association with celiac disease. Impaired XO activity would be expected to drive purines towards other degradation pathways. Adenosine deaminase (ADA), a cytoplasmic enzyme that is involved in the catabolism of purine bases, is elevated in celiac disease, and is therefore a useful diagnostic marker (Cakal et al., 2010). In fact, elevation of ADA is correlated with an increase in several inflammatory conditions. Impaired purine synthesis is expected in the context of cobalamin deficiency as well, because methyl melonlyl CoA mutase depends on catalytic action by cobalamin (Allen et al., 1993). Decreased purine synthesis results in impaired DNA synthesis, which then leads to megaloblastic anemia (Boss, 1985), due to slowed renewal of RBC's from multipotent progenitors, a problem that is compounded by suppressed EPO activity (Bergamaschi et al., 2008), a feature of celiac disease.

A remarkable recent case of a three-month old infant suffering from molybdenum deficiency links several aspects of glyphosate toxicity together, although glyphosate exposure was not considered as a possible cause in this case (Boles et al., 1993). This child presented with microcephaly, developmental delay, severe irritability, and lactic acidosis. Lactic acidosis is a striking feature of intentional glyphosate poisoning induced by drinking Roundup (Zouaoui et al., 2013; Beswick & Millo, 2011), and it suggests impaired oxidative respiration, as is seen in E. coli exposed to glyphosate (Lu et al., 2013). In vitro studies of glyphosate in the formulation Roundup have demonstrated an ability to disrupt oxidative respiration by inducing mitochondrial swelling and inhibiting mitochondrial complexes II and III (Peixoto, 2005). This would explain a massive build-up of lactic acid following ingestion of Roundup, due to a switch to anaerobic metabolism. Glyphosate has also been shown to uncouple mitochondrial phosphorylation in plants (Haderly et al., 1977; Ali & Fletcher, 1977).

As has been stated previously, microcephaly is a feature of excess RA, which could be induced by glyphosate due to its inhibitory action on CYP enzymes. In the case study on molybdenum deficiency (Boles et al., 1993), urinary sulfite levels were high, indicative of defective sulfite oxidase activity. Serum hypouricemia was also present, indicative of impaired XO activity. So, the induction of excess RA, depletion of molybdenum, and lactic acidosis by glyphosate provide a plausible environmental factor in this case.

One final aspect of molybdenum deficiency involves nitrate metabolism. As a source of nitric oxide, inorganic nitrite regulates tissue responses to ischemia. While nitrate reductase activity has been known to be a capability of microbes for many years, it has only recently been realized that mammals also possess a functioning nitrate reductase capability, utilizing a molybdenum-dependent enzyme to produce nitrite from nitrate (Jansson et al., 2008). Molybdenum deficiency would impair this capability, likely contributing to the higher risk to venous thrombosis observed in celiac disease (Zenjari et al., 1995; Marteau et al., 1994, Grigg, 1999). This could also explain the excess nitrates in the urine observed in association with celiac disease (Högberg et al., 2011).

8 Selenium and thyroid disorders

Autoimmune thyroid disease is associated with celiac disease (Collin et al., 2002; Valentino et al., 2002). In (Valentino et al., 2002), up to 43% of patients with Hashimoto's thyroiditis showed signs of mucosal T-cell activation typical of celiac disease. Selenium, whose deficiency is associated with celiac disease (Hinks et al., 1984), plays a significant role in thyroid hormone synthesis, secretion and metabolism, and selenium deficiency is therefore a significant factor in thyroid diseases (Sher, 2000; Chanoine et al., 2001; Khrle, 2013).

Selenium is required for the biosynthesis of the “twenty first amino acid,” selenocysteine. Twenty five specific selenoproteins are derived from this amino acid. Selenium deficiency can lead to an impairment in immune function and spermatogenesis in addition to thyroid function (Papp et al., 2007). One very important selenoprotein is glutathione peroxidase, which protects cell membranes and cellular components against oxidative damage by both hydrogen peroxide and peroxynitrite (ONOO^–) (Prabhakar et al., 2006).

Wheat can be a good source of selenoproteins. However, the content of selenium in wheat can range from sufficient to very low, depending upon soil physical conditions. Soil compaction, which results from modern practices of “no till” agriculture (Huggins & Reganold, 2008), can lead to both reduced selenium content and a significant increase in arsenic content in the wheat (Zhao et al., 2007). Since glyphosate has been shown to deplete sulfur in plants (Saes Zobiole et al., 2010), and selenium is in the same column of the periodic table as sulfur, it is likely that glyphosate also disrupts selenium uptake in plants. A gluten-free diet will guarantee, however, that no selenium is available from wheat, inducing further depletion of selenoproteins, and therefore increasing the risk to immune system, thyroid and infertility problems in treated celiac patients.

The gut bacterium Lactobacillus, which is negatively impacted by glyphosate (Shehata et al., 2013) and depleted in association with celiac disease (Di Cagno et al., 2011), is able to fix inorganic selenium into more bioavailable organic forms like selenocysteine and selenomethionine (Pessione, 2012). Selenocysteine is present in the catalytic center of enzymes that protect the thyroid from free radical damage (Triggiani et al., 2009). Free radical damage would lead to apoptosis and an autoimmune response (Tsatsoulis, 2002). Glyphosate's disruption of these bacteria would lead to a depletion in the supply of selenomethionine and selenocysteine. Methionine depletion by glyphosate (Nafziger et al., 1984) would further compound this problem.

Thus, there are a variety of ways in which glyphosate would be expected to interfere with the supply of selenoproteins to the body, including its effects on Lactobacillus, its depletion of methionine, the no-till farming methods that are possible because weeds are killed chemically, and the likely interference with plant uptake of inorganic selenium. This aligns well with the observed higher risk of thyroid problems in association with celiac disease, in addition to infertility problems and immune issues, which are discussed elsewhere in this paper. Further support for an association between glyphosate and thyroid disease comes from plots over time of the usage of glyphosate in the U.S. on corn and soy time-aligned with plots of the incidence rate of thyroid cancer in the U.S., as shown in Figure 3.

Figure 3

Thyroid cancer incidence rate plotted against glyphosate applied to U.S. corn & soy crops (R=0.988, p≤7.612e-09) along with % GE corn & soy crops (R=0.9377, p≤2.152e-05). Sources: USDA:NASS; SEER. (Figure courtesy of Nancy ...

9 Indole and kidney disease

The prevalence of kidney disease and resulting dialysis is increasing worldwide, and kidney disease is often associated with increased levels of celiac disease autoantibodies. Kidney disease and thyroid dysfunction are intimately connected (Iglesias & Díez, 2009). A population-based study in Sweden involving nearly 30,000 people with diagnosed celiac disease determined that there was nearly a three-fold increased risk for kidney failure in this population group (Welander et al., 2012).

Inflammation plays a crucial role in kidney disease progression (Tonelli et al., 2005; Bash et al., 2009; Rodriguez-Iturbe et al., 2010). Chronic kidney disease develops as a consequence of assaults on the kidney from inflammatory agents, brought on by the induction of pro-inflammatory cytokines and chemokines in the kidney. The toxic phenol p-Cresol sulfate, as well as indoxyl sulfate, a molecule that is chemically similar to p-Cresol, have been shown to induce activation of many of these cytokines and chemokines (Sun et al., 2012). p-Cresol and indoxyl sulfate both decrease endothelial proliferation and interfere with wound repair (Dou et al., 2004). p-Cresol is produced by the pathogenic bacterium C. difficile, and indoxyl sulfate, derived from indole through sulfation in the liver (Banoglu & King, 2002), accumulates at high levels in association with chronic kidney disease (Niwa, 2010).

The aromatic amino acid tryptophan contains an indole ring, and therefore disruption of tryptophan synthesis might be expected to generate indole as a by-product. Indeed, glyphosate has been shown to induce a significant increase in the production of indole-3-acetic acid in yellow nutsedge plants (Caal et al., 1987). Indole is produced by coliform microorganisms such as E. coli under anaerobic conditions. Glyphosate induces a switch in E. coli from aerobic to anaerobic metabolism due to impaired mitochondrial ATP synthesis (Lu et al., 2013; Samsel & Seneff, 2013), which would likely result in excess production of indole. Besides, E. coli, many other pathogenic bacteria can produce indole, including Bacillus, Shigella, Enterococcus, and V. cholerae (Lee & Lee, 2010). At least 85 different species of both Gram-positive and Gram-negative bacteria produce indole, and its breakdown by certain bacterial species depends on CYP enyzmes (Lee & Lee, 2010). Feeding indole to rats deprived of sulfur metabolites leads to macrocytic anemia (Roe, 1971). Indole is an important biological signaling molecule among microbes (Lee & Lee, 2010). Indole acetic acid inhibits the growth of cobalamin-dependent microorganisms, which then causes macrocytic (pernicious) anemia in the host due to cobalamin deficiency (Drexler, 1958).

Experiments on exposure of mouse fetuses to indole-3-acetic acid have shown that it dramatically induces microcephaly in developing fetuses exposed at critical times in development (Furukawa et al., 2007). A case study found celiac disease associated with microcephaly and developmental delay in a 15-month-old girl (Bostwick et al., 2001; Lapunzina, 2002). A gluten-free diet restored head growth. The authors suggested that poor head growth might precede other manifestations of celiac disease in infants. A study on plants demonstrated a concentration gradient of indole-3-acetic acid in the plant embryo, similar to the gradient in retinoic acid that controls fetal development in mammals (Uggla et al., 1996). This alternative may be another way in which glyphosate would promote microcephaly.

Thus, solely through its effect on indole production and indole catabolism in gut bacteria, chronic glyphosate exposure would be expected to lead to cobalamin deficiency, pernicious anemia, microcephaly in a fetus during pregnancy, and kidney failure. p-Cresol supply by overgrown pathogens like C. difficile would likely contribute in a similar way as indole, due to its similar biochemical and biophysical properties.

10 Nutritional deficiencies

The damaged villi associated with celiac disease are impaired in their ability to absorb a number of important nutrients, including vitamins B6, B12 (cobalamin) and folate, as well as iron, calcium and vitamins D and K (Hallert et al., 2002). Thus, long-term celiac disease leads to major deficiencies in these micronutrients. Cobalamin deficiency has been well addressed previously. We have also already mentioned the chelation of trace minerals by phytates and by glyphosate. However, other factors may be at play as well, as discussed here.

Glyphosate disrupts the synthesis of tryptophan and tyrosine in plants and in gut bacteria, due to its interference with the shikimate pathway (Lu et al., 2013; María et al., 1996), which is its main source of toxicity to plants. Glyphosate also depletes methionine in plants and microbes. A study on serum tryptophan levels in children with celiac disease revealed that untreated children had significantly lower ratios of tryptophan to large neutral amino acids in the blood, and treated children also had lower levels, but the imbalance was less severe (Hernanz & Polanco, 1991). The authors suggested a metabolic disturbance in tryptophan synthesis rather than impaired absorption, as other similar amino acids were not deficient in the serum. It was proposed that this could lead to decreased synthesis of the monoamine neurotransmitter, serotonin, in the brain associated with behavior disorders in children with celiac disease, such as depression (Koyama & Melzter, 1986). Deficiencies in tyrosine and methionine were also noted (Hernanz & Polanco, 1991). “Functional dyspepsia” is an increasing and mainly intractable problem in the Western world, which is estimated to affect 15% of the U.S. population (Saad & Chey, 2006). Dyspepsia, a clinical symptom of celiac disease, is likely mediated by excess serotonin synthesis following ingested tryptophan-containing foods (Manocha et al., 2012).

Serotonin (5-hydroxytryptamine or 5-HT) is produced by enterochromaffin (EC) cells in the gut and is an important signaling molecule for the enteric mucosa (Kim et al., 2001). EC cells are the most numerous neuroendocrine cell type in the intestinal lumen, and they regulate gut secretion, motility, pain and nausea by activating primary afferent pathways in the nervous system (Chin et al., 2012). Serotonin plays an important role in activating the immune response and inflammation in the gut, and also induces nausea and diarrhea when it is overexpressed. Anaerobic bacteria in the colon convert sugars into short-chain fatty acids, which can stimulate 5-HT release from EC cells (Fukumoto et al., 2003; Grider & Piland, 2007). This is likely an important source of fats to the body in the case of a low-fat diet induced by impaired fatty acid metabolism due to insufficient bile acids.

The number of 5-HT expressing EC cells in the small intestine is increased in association with celiac disease, along with crypt hyperplasia (Wheeler & Challacombe, 1984; Challacombe et al., 1977), and, as a consequence, serotonin uptake from dietary sources of tryptophan is greatly increased in celiac patients (Erspamer, 1986). Postprandial dyspepsia is associated in celiac disease with increased release of 5-HT, and this may account for the digestive symptoms experienced by celiac patients (Coleman et al., 2006). An explanation for these observations is that a chronic tryptophan insufficiency due to the impaired ability of gut bacteria to produce tryptophan induces aggressive uptake whenever dietary tryptophan is available.

Glyphosate forms strong complexes with transition metals, through its carboxylic, phosphonic, and amino moieties, each of which can coordinate to metal ions, and it can also therefore form complexes involving two or three atoms of the targeted transition metal (Madsen et al., 1978; Motekaitis & Martell, 1985; Undabeytia et al., 2002). This means that it is a metal chelator par excellence. One can expect, therefore, deficiencies in multiple transition (trace) metals, such as iron, copper, cobalt, molybdenum, zinc and magnesium in the presence of glyphosate. Glyphosate has been shown to reduce levels of iron, magnesium, manganese and calcium in non-GMO soybean plants (Cakmak et al., 2009). We have already discussed iron, selenium, cobalt and molybdenum deficiencies in association with celiac disease.

Zinc deficiency seems to be a factor in celiac disease, as a recent study of 30 children with celiac disease demonstrated a significantly reduced serum level of zinc (0.64 vs 0.94 µg/mL in controls) (Singhal et al., 2008). Copper deficiency is a feature of celiac disease (Halfdanarson et al., 2009), and copper is one of the transition metals that glyphosate binds to and chelates (Madsen, 1978; Undabeytia, 2002). Confirmed magnesium deficiency in celiac disease has been shown to be due to significant loss through the feces (Goldman et al., 1962). This would be expected through binding to phytates and/or glyphosate. A study of 23 patients with gluten-sensitive enteropathy to assess magnesium status revealed that only one had serum magnesium levels below the normal range, whereas magnesium levels in erythrocytes and lymphocytes was markedly below normal, and this was associated with evidence of osteoporosis due to malabsorption (Rude and Olerich, 1996). Daily treatment with MgCl₂ or Mg lactate led to a significant increase in bone mineral density, and was correlated with a rise in RBC Mg²⁺.

A recent study investigated the status of 25(OH) vitamin D3 in adults and children with celiac disease (Lerner et al., 2012). It was determined that vitamin D3 deficiency was much more prevalent in the adults than in the children, suggesting a deterioration in vitamin D3 serum levels with age. This could be explained by a chronic accumulation of glyphosate, leading to increasingly impaired vitamin D3 activation in the liver. The liver converts 1,25(OH) vitamin D3 to the active form, 25(OH) vitamin D3, using CYP27A (Ponchon et al., 1969; Sakaki et al., 2005), which might be disrupted by glyphosate exposure, given its known interference with CYP function in mice (Hietanen et al., 1983). On a broader level, this might also explain the recent epidemic in the U.S. in vitamin D3 deficiency (Holick, 2005).

Another issue to consider is whether the food being consumed by celiac patients is itself depleted in nutrients. This is likely the case for the transgenic Roundup-Ready crops that increasingly supply the processed food industry. A recent study on the effects of glyphosate on Roundup-Ready soy revealed a significant effect on growth, as well as an interference with the uptake of both macronutrients and micronutrients (Saes Zobiole et al., 2010). Transgenic soybeans exposed to glyphosate are often affected by a “yellow flashing” or yellowing of the upper leaves, and an increased sensitivity to water stress. An inverse linear relationship was observed between glyphosate dosage and levels of the macronutrients, sodium, calcium, sulfur, phosphorus, potassium, magnesium, and nitrogen, as well as the micronutrients, iron, zinc, manganese, copper, cobalt, molybdenum, and boron. Glyphosate's ability to form insoluble metal complexes likely mediates these depletions (Glass, 1984). Glyphosate also interferes with photosynthesis, as reflected in several measures of photosynthesis rate (Saes et al., 2010) and reductions in chlorophyll (Ali & Fletcher, 1977; Kitchen et al., 1981). This could be due to depletion of zinc and manganese, since chloroplasts require these micronutrients to function well (Homann, 1967; Thompson & Weier, 1962).

11 Cancer

Chronic inflammation, such as occurs in celiac disease, is a major source of oxidative stress, and is estimated to account for 1/3 of all cancer cases worldwide (Ames et al., 1993; Coussens & Werb, 2002). Oxidative stress leads to DNA damage and increased risk to genetic mutation. Several population-based studies have confirmed that patients with celiac disease suffer from increased mortality, mainly due to malignancy (Nielsen et al., 1985; Logan et al., 1989; Pricolo et al., 1998; Cottone et al., 1999; Corrao et al., 2001; Green et al., 2003). These include increased risk to non-Hodgkin's lymphoma, adenocarcinoma of the small intestine, and squamous cell carcinomas of the esophagus, mouth, and pharynx, as well as melanoma. The non-Hodgkin's lymphoma was not restricted to gastrointestinal sites, and the increased risk remained following a gluten-free diet (Green et al., 2003).

Celiac disease is associated with a lifelong risk of any malignancy between 8.1 and 13.3%, with the risk for non-Hodgkin's lymphoma alone being 4.3 to 9.6% (Matheus-Vliezen et al., 1994; Egan et al., 1995). This risk is 19-fold higher than the risk in the general population. Selenium deficiency in association with celiac disease may be a significant factor in the increased cancer risk. Selenium deficiency is associated with increased risk to several cancers, and selenium supplements are beneficial in reducing the incidence of liver cancer and decreasing mortality in colorectal, lung and prostate cancer (Nelson et al., 1999; Björnstedt et al., 2010).

Children with celiac disease, whether or not they are on a gluten-free diet, exhibit elevated urinary biomarkers of DNA damage (Zaflarska-Popawska et al., 2010). Human colon carcinoma cells exposed to peptides extracted from wheat responded with a sharp increase in the GSSG/GSH ratio (ratio of oxidized to reduced glutathione), a well-established indicator of oxidative stress (Rivabene, 1999). The authors did not provide information as to whether the wheat plants were exposed to glyphosate, but they did suggest that this effect could explain the increased risk to intestinal cancer associated with celiac. Intriguingly, studies on pea plants have shown that glyphosate induces a sharp increase in the GSSG/GSH ratio in plants (Miteva et al., 2003), which suggests that glyphosate contamination could explain the results observed in (Rivabene, 1999).

Interestingly, it was noted in 1996 that the incidence of both non-Hodgkin's lymphoma and melanoma had been rising sharply worldwide in recent decades, and so it was decided to investigate whether there might be a link between the two cancers associated with sunlight exposure. Surprisingly, the authors found an inverse relationship between non-Hodgkin's lymphoma and UV exposure. More recently, such UV protection has been reaffirmed in a review of epidemiologic studies on the subject (Negri, 2010). This suggests that vitamin D3 is protective, so vitamin D3 deficiency due to impaired CYP function in the liver could be contributory to increased risk in celiac disease.

The incidence of non-Hodgkins lymphoma has increased rapidly in most Western countries over the last few decades. Statistics from the American Cancer Society show an 80% increase since the early 1970's, when glyphosate was first introduced on the market.

While there have been only a few studies of lymphoma and glyphosate, nearly all have indicated a potential relationship (Vigfusson & Vyse, 1980; Pavkov & Turnier, 1986; Hardell & Eriksson, 1999; McDuffie et al., 2001; De Roos et al., 2003). A dose-response relationship for non-Hodgkin's lymphoma was demonstrated in a cross-Canada study of occupational exposure to glyphosate in men (McDuffie et al., 2001), and a larger study in the U.S. noted a similar result (De Roos et al., 2003). A population-based study in Sweden showed an increased risk to non-Hodgkins lymphoma upon prior exposure to herbicides and fungicides but not insecticides (Hardell & Eriksson, 1999). Glyphosate exposure resulted in an odds ratio of 2.3, although the number of samples was small, and the authors suggested that further study is necessary. A study on mice showed increases in carcinoma, leukemia and lymphoma (Pavkov & Turnier, 1986) and an in vitro mutagenic test on human lymphocytes revealed increased sister-chromatid exchanges (Vigfusson & Vyse, 1980) upon exposure to glyphosate.

12 Proposed transglutaminase-glyphosate interactions

Establishing the mechanism by which glyphosate might promote autoantibodies to transglutaminase is a challenging task, not because this possibility seems unlikely but rather because multiple disruptions are plausible. In this section, we present evidence from the research literature that supports various hypotheses for the interaction of glyphosate with the transglutaminase enzymatic pathways. The definitive studies that clarify which of these hypotheses is correct have yet to be conducted.

Celiac disease is thought to be primarily caused by ingestion of wheat gluten proteins, particularly gliadin, due to a high concentration of proline- and glutamine-rich sequences, which imparts resistance to degradation by proteases. Transglutaminase autoimmunity arises when specific epitopes of wheat gliadin activate sensitized T-cells which then stimulate B-cell synthesis of IgA or IgM autoantibodies to transglutaminase. Transglutaminase bound to gliadin can induce false recognition by a T-cell.

Transglutaminase acts on gluten in wheat to form crosslinks between glutamine residues and lysine residues, producing ammonia as a by-product. Ammonia is known to induce greater sensitivity to glyphosate in plants, and it is common practice to apply ammonium sulfate simultaneously with glyphosate for this reason (Nalewaja & Matysiak, 1993). This enhanced effect is due to ammonium binding to glyphosate at three sites – one on the carbonyl group and two on the phosphonyl group, which displaces cations such as calcium and endows glyphosate with enhanced reactivity.

Transglutaminase sometimes only achieves half of its intended reaction product, by converting a glutamine residue to glutamate, and leaving lysine intact, thus not producing the desired crosslink. It has been established that gluten fragments containing “deamidated glutamine” residues instead of the crosslinks are much more highly allergenic than those that contain the crosslinks (Dørum et al., 2010; Qiao et al., 2005). These have been referred to as “celiac disease T-Cell epitopes.” T-cells of celiac patients preferentially recognize epitopes that are augmented with negatively charged deamidated glutamine residues – the product of the reaction when the lysine linkage does not occur. Thus, if there is a mechanism by which glyphosate interferes with crosslink formation, this would explain its ability to enhance gluten sensitivity.

A clue can be found from the research literature on glyphosate sensitivity in plants, where it has been determined that the substitution of a lysine residue in a critical locale in EPSP synthase greatly increases sensitivity to glyphosate (Selvapandiyan et al., 1995). Lysine's NH3+ group is highly reactive with negatively charged ions, and this makes it a common constituent of DNA binding proteins due to its ability to bind to phosphates in the DNA backbone. Glyphosate contains a phosphonyl group that binds easily to ammonia and behaves as a phosphate mimetic. It also contains a carboxyl group that substitutes well for the carboxyl group of glutamate, the intended reaction partner.

Thus, it seems possible that glyphosate would be drawn to the ammonia released when the glutamine residue is deamidated by transglutaminase, and then the ammonium glyphosate would react with the lysine residue, releasing the ammonia and resulting in the binding of glyphosate to the lysine residue. This would yield a gluten fragment bound to glyphosate that is likely highly allergenic. An analogous EPSP synthase-EPSP-glyphosate ternary complex has been identified in numerous studies on the physiology of glyphosate in plants (Sammons et al., 1995).

Research in the food industry has concerned producing breads that, while not gluten free, may contain forms of gluten to which celiac patients are less sensitive. Such research has revealed that enzymatic modification to promote methionine binding to glutamine reduces IgA immunoreactivity (Cabrera-Chávez et al., 2010). Whether methionine binding to glutamine residues in wheat takes place in vivo is not known, but it is established that glyphosate depletes methionine by 50 to 65 percent in plants, as well as the aromatic amino acids (Nafziger et al., 1984; Haderlie et al., 1977). As we have already discussed, glyphosate interferes with cobalt bioavailability for cobalamin synthesis, and cobalamin is an essential catalyst for the conversion of cysteine to methionine.

Transglutaminase also cross-links proteins in the extracellular matrix, and therefore is important for wound healing, tissue remodeling, and stabilization of the extracellular matrix. Thus, autoimmunity to transglutaminase leads to destabilization of the microvilli lining the small intestines. Transglutaminase has 18 free cysteine residues which are targets for S-nitrosylation. A cysteine residue is also involved in the catalytic active site. A unique Ca²⁺ dependent mechanism regulates nitrosylation by NO, mediated by CysNO (S-nitrosocysteine). It was shown experimentally that up to 15 cysteines of transglutaminase were nitrosylated by CysNO in the presence of Ca²⁺, and this inhibited its enzymatic activity (Lai et al., 2001).

Thus, another plausible mechanism by which glyphosate might enhance the development of autoantibodies to transglutaminase is by nitrosylating its cysteines, acting similarly to CysNO. A precedent for this idea is set with research proposing nitrosylation as the means by which glyphosate interferes with the heme active site in CYP enzymes (Lamb et al., 1998). It is conceivable that cysteine nitrosylation by glyphosate at the active site inactivates the molecule, in which case glyphosate is itself acting as an “antibody.”

13 Evidence of glyphosate exposure in humans and animals

The US EPA has accepted Monsanto's claim that glyphosate is essentially harmless to humans. Due to this position, there have been virtually no studies undertaken in the US to assess glyphosate levels in human blood or urine. However, a recent study involving multiple countries in Europe provides disturbing confirmation that glyphosate residues are prevalent in the Western diet (Hoppe, 2013). This study involved exclusively city dwellers, who are unlikely to be exposed to glyphosate except through food sources. Despite Europe's more aggressive campaign against GMO foods than that in the Americas, 44% of the urine samples contained quantifiable amounts of glyphosate. Diet seems to be the main source of exposure. One can predict that, if a study were undertaken in the U.S., the percentage of the affected population would be much larger.

A recent study conducted on dairy cows in Denmark shows conclusively that the cows’ health is being adversely affected by glyphosate (Krüger et al., 2013a). All of the cows had detectable levels of glyphosate in their urine, and it was estimated that from 0.1 to 0.3 mg of glyphosate was excreted daily from each cow. More importantly, all of the cows had serum levels of cobalt and manganese that were far below the minimum reference level for nutrient sufficiency. Half of the cows had high serum urea, and there was a positive linear relationship between serum urea and glyphosate excretion. High serum urea is indicative of nephrotoxicity. Blood serum levels of enzymes indicative of cytotoxicity such as creatine kinase (CK) and alkaline phosphatase (ALP) were also elevated. CK is indicative of rhabdomyolysis or kidney failure. High levels of ALP indicate liver damage, and it is often used to detect blocked bile ducts (Kaplan et al., 1983).

Thus, the low cobalt levels and the indicators of liver, kidney, and gall bladder stress are all consistent with our previous discussion. The results of this study were also consistent with results of a study on rats exposed experimentally to glyphosate (Beuret et al., 2005) in which Roundup was shown to be even more toxic than its active ingredient, glyphosate.

Glyphosate-metal complexes serve to reduce glyphosate's toxicity in the soil to plants, but they also protect glyphosate from attack by microorganisms that could decompose it (Cusiel, 2005). The degree of reactivity of the complex depends on which metals glyphosate binds to, which in turn depends upon the particular soil conditions (Nomura & Hilton, 1977). Glyphosate usually degrades relatively quickly (Vencill, 2002); however, a half-life of up to 22 years has also been reported in conditions where pH is low and organic matter contents are high (Nomura & Hilton, 1977). Therefore, glyphosate may survive much longer in certain soils than has been claimed by the industry, and could be taken up by crops planted subsequent to glyphosate application to kill weeds.

A disturbing trend of crop desiccation by glyphosate pre-harvest (O'Keeffe, 1980; O'Keeffe, 1981; Stride et al., 1985; Darwent et al., 1994; Orson & Davies, 2007) may be a key factor in the increased incidence of celiac disease. According to Monsanto, glyphosate was used on some 13% of the wheat area pre-harvest in the UK in 2004. However, by 2006 and 2007, some 94% of UK growers used glyphosate on at least 40% of cereal and 80% of oilseed crops for weed control or harvest management (Monsanto International Sàrl, 2010).

An increasing number of farmers now consider the benefits of desiccating their wheat and sugar cane crops with glyphosate shortly before the harvest (Monsanto International Sàrl, 2010). The advantage is improved harvesting efficiency because the quantity of materials other than grain or cane is reduced by 17%, due to a shutdown of growth following glyphosate treatment. Treated sugar cane crops produce drier stalks which can be baled more easily. There is a shorter delay before the next season's crop can be planted, because the herbicide was applied pre-harvest rather than post-harvest. Several pests can be controlled due to the fact that glyphosate is a broad-spectrum herbicide. These include Black grass, Brome grasses, and Rye grasses, and the suggestion is that this would minimize the risk of these weeds developing resistance to other herbicides.

A complete list of the latest EPA residue levels for glyphosate as of September 18, 2013 are shown in Table 1. Tolerances are established on all crops for both human and animal consumption resulting from the application of glyphosate.

Table 1

Complete list of glyphosate tolerances for residues in food crops in the U.S. as of September 18, 2013, as reported in: EPA: Title 40: Protection of Environment.

As glyphosate usage continues unabated, glyphosate resistance among weeds is becoming a growing problem (Waltz, 2010), necessitating a strategy that either involves an increase in the amount of glyphosate that is applied or a supplementation with other herbicides such as glufosinate, dicampa, 2-4D, or atrazine. Agrochemical companies are now actively developing crops with resistance to multiple herbicides (Culpepper, 2000), a disturbing trend, especially since glyphosate's disruption of CYP enzymes leads to an impaired ability to break down many other environmental chemicals in the liver.

14 Kidney disease in agricultural workers

Chronic kidney disease is a globally increasing problem (Ramirez-Rubio et al., 2013), and glyphosate may be playing a role in this epidemic. A plot showing recent trends in hospitalization for acute kidney injury aligned with glyphosate usage rates on corn and soy shows strong correlation, as illustrated in Figure 4, and a similar correlation is seen for deaths due to end-stage renal disease in Figure 5. Recently, it has been noted that young men in Central America are succumbing in increasing numbers to chronic kidney disease (Trabanino et al., 2002; Cerdas, 2005; Torres et al., 2010; Peraza et al., 2012; Ramirez-Rubio et al., 2013; Sanoff et al., 2010). The problem appears to be especially acute among agricultural workers, mainly in sugar cane fields (Cerdas, 2005; Torres et al., 2010; Peraza et al., 2012). Since we have shown in Section 8 how glyphosate can produce toxic effects on the kidneys through its disruption of gut bacteria, it is fruitful to consider whether glyphosate could be playing a role in the fate of Central American workers in the sugar cane fields.

Figure 4

Number of hospitalizations for acute kidney injury plotted against glyphosate applied to com & soy (in 1000 tons). (Figure courtesy of Nancy Swanson).

Figure 5

End stage renal disease deaths (ICD N18.0 & 585.6) plotted against % GE corn & soy planted (R=0.9585, p<4.03e-6) and glyphosate applied to corn & soy (R=0.9844, p≤3.704e-09). Sources: USDA:NASS; CDC. (Figure courtesy ...

In attempting to explain this phenomenon, physicians and pharmacists have proposed that it may be due to dehydration caused by over-exertion in high temperature conditions, combined with an acute reaction to commonly administered non-steroidal anti-inflammatory drugs (NSAIDs) to treat pain and/or antibiotics to treat infection (Ramirez-Rubio et al., 2013). NSAIDs require CYP enzymes in the liver for detoxification (Agúndez et al., 2009), so impaired CYP function by glyphosate would lead to a far more toxic effect of excessive NSAID administration. Kidney disease among agricultural workers tends to be associated with chronic glomerulonephritis and interstial nephritis, which was proposed in (Soderland et al., 2010) to be due to environmental toxins such as heavy metals or toxic chemicals. Glomerulonephritis is also found in association with celiac disease (Katz et al., 1979; Peters et al., 2003). A Swedish study showed a five-fold increase in nephritis risk in celiac patients (Peters et al., 2003).

A strong hint comes from epidemiological studies conducted in Costa Rica (Cerdas, 2005). The demographic features of those with chronic renal failure revealed a remarkably specific pattern of young men, between 20 and 40 years old, with chronic interstitial nephritis. All of them were sugar-cane workers. These authors wrote: ”A specific study of their work environment is needed to determine what in their daily activities puts them at increased risk for chronic renal failure.”

Agriculture is an important part of the economy of the state of Louisiana in the United States, and sugar cane is a significant agricultural product. Chemical methods to ripen sugar cane are commonly used, because they can substantially increase the sucrose content of the harvest (Richard & Dalley, 2009). Glyphosate, in particular, has been the primary ripener used in Louisiana since 1980 (Orgeron, 2012). As of 2001, Louisiana had the highest rate of kidney failure in the U.S. (State-Specific Trends in Chronic Kidney Failure – United States, 1990–2001). Louisiana's death rate per 100,000 from nephritis/kidney disease is 26.34 as compared to a U.S. rate of 14.55 (Network Coordinating Council, 2013). The number of patients on dialysis has risen sharply in the last few years.

By 2005, it is estimated that 62% of the total harvested hectares of sugar cane in Louisiana were ripened with glyphosate (Legendre et al., 2005). A paper published in 1990 showed that glyphosate applied as a ripener on three different sugar cane varieties grown in Costa Rica produced up to a 15% increase in the sucrose content of the harvested sugar cane (Subiros, 1990). Glyphosate applied before the harvest is the only sugarcane ripener currently registered for use in the U.S.

A disturbing recent trend is the repeated application of glyphosate over the course of the season with the hope of further increasing yields (Richard & Dalley, 2009). Responses to the standard application rate (0.188 lb/acre) of glyphosate have been inconsistent, and so farmers are increasing both the amount and the frequency of application. In (Richard & Dalley, 2009), growers are encouraged not to apply glyphosate beyond mid-October, as results are counterproductive, and not to use higher rates in an attempt to improve yield. But it is doubtful that these recommendations are being followed. It is likely, although we have not been able to confirm this, that glyphosate usage has expanded in scope on the sugar cane fields in Central America since 2000, when the expiration of Monsanto's patent drove prices down, and that the practices of multiple applications of glyphosate in the U.S. are also being followed in Central America. Several other ripening agents exist, such as Ethephon, Trinexapacethyl, and Sulfometuron-methyl, but glyphosate is likely growing in popularity recently due to its more favorable pricing and perceived non-toxicity. Larger amounts are needed for effective ripening in regions that are hot and rainy, which matches the climate of Costa Rica and Nicaragua.

15 Discussion

In this paper, we have developed an argument that the alarming rise in the incidence of celiac disease in the United States and elsewhere in recent years is due to an increased burden of herbicides, particularly glyphosate exposure in the diet. We suggest that a principal factor is the use of glyphosate to desiccate wheat and other crops prior to the harvest, resulting in crop residue and increased exposure. Strong evidence for a link between glyphosate and celiac disease comes from a study on predatory fish, which showed remarkable effects in the gut that parallel the features of celiac disease (Shenapati et al., 2009).

More generally, inflammatory bowel disease has been linked to several environmental factors, including a higher socioeconomic status, urban as opposed to rural dwelling, and a “Westernized” cultural context (Shapira et al., 2010). Disease incidence is highest in North America and Europe, and is higher in northern latitudes than in southern latitudes within these regions, suggesting a beneficial role for sunlight. According to the most recent statistics from the U.S. Environmental Protection Agency (EPA) (Grube et al., 2011), the U.S. currently represents 25% of the total world market on herbicide usage. Glyphosate has been the most popular herbicide in the U.S. since 2001, whereas it was the 17th most popular herbicide in 1987 (Kiely et al., 2004). Since 2001, glyphosate usage has grown considerably, due to increased dosing of glyphosate-resistant weeds and in conjunction with the widespread adoption of “Roundup-Ready” genetically modified crops. Glyphosate is probably now the most popular herbicide in Europe as well (Kimmel et al., 2013). Glyphosate has become the number one herbicide worldwide, due to its perceived lack of toxicity and its lower price after having become generic in 2000 (Duke & Powles, 2008).

A recent estimate suggests that one in twenty people in North America and Western Europe suffer from celiac disease (Koning, 2005; Fasano et al., 2003). Outdoor occupational status is protective (Sonnenberg et al., 1991). First generation immigrants into Europe or North America are generally less susceptible, although second generation non-Caucasian immigrants statistically become even more susceptible than native Caucasians (Shapira et al., 2010). This may in part stem from the increased need for sunlight exposure given darker skin pigmentation.

Table 2 summarizes our findings relating glyphosate to celiac disease. All of the known biological effects of glyphosate – cytochrome P450 inhibition, disruption of synthesis of aromatic amino acids, chelation of transition metals, and antibacterial action – contribute to the pathology of celiac disease.

Table 2

Illustration of the myriad ways in which glyphosate can be linked to celiac disease or its associated pathologies.

(b) Transition metal chelation

(c) CYP enzyme inhibition

(d) Shikimate pathway suppression

Celiac disease is associated with deficiencies in several essential micronutrients such as vitamin D3, cobalamin, iron, molybdenum, selenium and the amino acids, methionine and tryptophan, all of which can be explained by glyphosate. Glyphosate depletes multiple minerals in both genetically modified soybeans (Saes et al., 2010) and conventional soybeans (Cakmak et al., 2009), which would translate into nutritional deficiencies in foods derived from these crops. This, together with further chelation in the gut by any direct glyphosate exposure, could explain deficiencies in cobalt, molybdenum and iron. Glyphosate's effect on CYP enzymes should lead to inadequate vitamin D3 activation in the liver (Hietanen et al., 1983; Ponchon et al., 1969). Cobalamin depends on cobalt, and cobalt-dependent enzymes in plants and microbes have been shown to be inhibited by glyphosate (Bode et al., 1984; Ganson and Jensen, 1988). Glyphosate has been shown to severely impair methionine and tryptophan synthesis in plants (Nafziger et al., 1984), which would reduce the bioavailability of these nutrients in derived foods.

There are multiple intriguing connections between celiac disease and microcephaly, all of which can be linked to glyphosate. Celiac disease is found in association with microcephaly in infants (Bostwick et al., 2001; Lapunzina, 2002), and teratogenic effects are also observed in children born to celiac mothers (Dickey et al., 1996; Martinelli et al., 2000). Microcephaly in an infant where confirmed molybdenum deficiency was present (Boles et al., 1993) suggests that molybdenum deficiency could be causal. However, elevated RA also induces microcephaly, as does indole-3-acetic acid, which has been dramatically linked to microcephaly in mice (Furukawa et al., 2007). Elevated RA is predicted as a response to glyphosate due to its expected inhibition of CYP enzymes which catabolize RA in the liver (Lamb et al., 1998; Hietanen et al., 1983). Molybdenum deficiency is expected due to glyphosate's ability to chelate cationic minerals. Glyphosate has been shown to induce indole-3-acetic acid synthesis in plants (Caal et al., 1987), and it induces a shift to anaerobic metabolism in E. coli (Lu et al., 2013), which is associated with indole synthesis.

Celiac disease is associated with impaired serotonin metabolism and signaling in the gut, and this feature leads us to propose a novel role for serotonin in transporting sulfate to the tissues. It is a curious and little known fact that glucose and galactose, but not fructose or mannose, stimulate 5-HT synthesis by EC cells in the intestinal lumen (Kim et al., 2001), suggesting a role for EC cells as “glucose sensors.” Glucose and galactose are the two sugars that make up the heparan sulfate chains of the syndecans and glypicans that attach to the membrane-bound proteins in most cells, serving as the innermost constituency of the extracellular matrix (Bernfield et al., 1999). In (Seneff et al., 2012), it was proposed that part of the post-prandial glucose that is taken up by the tissues is temporarily stored in the extracellular matrix as heparan sulfate, and that a deficiency in sulfate supply impairs this process, which impedes glucose uptake in cells. These heparan sulfate units have a high turnover rate, as they are typically broken down within three hours of their initial placement (Turnbull et al., 2001). This provides the cells with a convenient temporary buffer for glucose and galactose that can allow them to more efficiently remove these sugars from the serum. Insufficient sulfate supplies would impair this process and lead to insulin resistance.

As is the case for other monoamine neurotransmitters as well as most sterols, 5-HT is normally transported in the serum in a sulfated form. The sulfate moiety must be removed for the molecule to activate it. Therefore, 5-HT, as well as these other monoamine neurotransmitters and sterols, can be viewed as a sulfate “escort” in the plasma. In (Samsel & Seneff, 2013), it was argued that such carbon-ring-containing molecules are necessary for safe sulfate transport, especially in the face of co-present kosmotropes like glyphosate, in order to protect the blood from excess viscosity during transport. Support for the concept that glyphosate gels the blood comes from the observation that disseminated coagulation is a characteristic feature of glyphosate poisoning (Zouaoui et al., 2013). Since glyphosate disrupts sterol sulfation and it disrupts monoamine neurotransmitter synthesis, in addition to its physical kosmotropic feature, it can be anticipated that a chronic exposure to even a small amount of glyphosate over the course of time will lead to a system-wide deficiency in the supply of sulfate to the tissues. We believe that this is the most important consequence of glyphosate's insidious slow erosion of health.

An interesting consideration regarding a known link between celiac disease and hypothyroidism (Collins et al., 2012) emerges when one considers that iodide is one of the few chaotropic (structure breaking) anions available to biological systems: another important one being nitrate, which is elevated in the urine in association with celiac disease (Laurin et al., 2003). It is intriguing that the conversion of T4 to T3 (the active form of thyroid hormone) involves selenium as an essential cofactor. Furthermore, iodide is released in the process, thus providing chaotropic buffering in the blood serum. Therefore, impaired conversion due to deficient selenium results in an inability to buffer this significant chaotrope in the blood, despite the fact that chaotropic buffering is likely desperately needed in the context of the kosmotropic effects of glyphosate. While speculative, it is possible that the autoimmune thyroid disease that develops in association with celiac disease is a direct consequence of the inability to activate thyroid hormone due to insufficient selenium. Indeed, celiac patients with concurrent hypothyroidism require an elevated dose of levothyroxine (T4) compared to non-celiac hypothyroid patients (Collins et al., 2012), which could be due to impaired activation to T3.

The link between autoimmune (type 1) diabetes and autoimmune thyroiditis is likely tied to deficiencies in selenoproteins leading to apoptosis. Diabetic rats produce significantly less glomerular heparan sulfate in the kidneys than controls, and this is associated with increased albuminurea (Jaya et al., 1993). However, children with type-1 diabetes and celiac disease excrete lower levels of albumin than type-1 diabetic children without celiac disease, suggesting a protective role for celiac disease (Gopee et al., 2013). Wheat is a good source of tryptophan, so it is likely that tryptophan-derived serotonin induces the symptoms of diarrhea and nausea associated with wheat ingestion, but, at the same time, transports available sulfate through the vasculature, to help maintain adequate supplies of heparan sulfate to the glomerulus. Thus, the increased metabolism of dietary tryptophan to serotonin observed in association with celiac disease may help ameliorate the sulfate deficiency problem. Glyphosate's interference with CYP enzymes links to impaired bile-acid production in the liver, which in turn impairs sterol-based sulfate transport, placing a higher burden on serotonin for this task.

We have argued here that kidney failure, a known risk factor in celiac disease, is a consequence of depleted sulfate supplies to the kidneys. An alarming increase in kidney failure in young male agricultural workers in sugar cane fields in South America can be directly linked to the recent increase in the practice of using Roundup to “ripen” the crop just prior to the harvest. Furthermore, glyphosate's interference with selenoprotein supply would lead to thyroid dysfunction, which greatly increases risk to kidney disease. We propose here that glyphosate is the key environmental factor contributing to this epidemic, but further investigation is warranted.

While we have covered a broad range of pathologies related to celiac disease in this paper, and have shown how they can be explained by glyphosate exposure, there are likely still other aspects of the disease and the connection to glyphosate that we have omitted. For example, in a remarkable case study (Barbosa, 2001), a 54-year-old man who accidentally sprayed himself with glyphosate developed skin lesions six hours later. More significantly, one month later he exhibited symptoms of Parkinson's disease. Movement disorders such as Parkinsonism are associated with gluten intolerance (Baizabal-Carvallo, 2012). Figure 6 shows plots of glyphosate application to corn and soy alongside plots of deaths due to Parkinson's disease. These and other connections will be further explored in future research.

Figure 6

Deaths from Parkinson's disease (ICD G20 & 332.0) plotted against glyphosate use on corn & soy (R=0.9006, p≤5.063e-07) and % GE corn & soy planted (R=0.9676, p≤2.714e-06). Sources: USDA:NASS; CDC. (Figure courtesy ...

16 Conclusion

Celiac disease is a complex and multifactorial condition associated with gluten intolerance and a higher risk to thyroid disease, cancer and kidney disease, and there is also an increased risk to infertility and birth defects in children born to celiac mothers. While the principal diagnostic is autoantibodies to tissue transglutaminase, celiac disease is associated with a spectrum of other pathologies such as deficiencies in iron, vitamin D3, molybdenum, selenium, and cobalamin, an overgrowth of pathogens in the gut at the expense of beneficial biota, impaired serotonin signaling, and increased synthesis of toxic metabolites like p-Cresol and indole-3-acetic acid. In this paper, we have systematically shown how all of these features of celiac disease can be explained by glyphosate's known properties. These include (1) disrupting the shikimate pathway, (2) altering the balance between pathogens and beneficial biota in the gut, (3) chelating transition metals, as well as sulfur and selenium, and (4) inhibiting cytochrome P450 enzymes. We argue that a key system-wide pathology in celiac disease is impaired sulfate supply to the tissues, and that this is also a key component of glyphosate's toxicity to humans.

The monitoring of glyphosate levels in food and in human urine and blood has been inadequate. The common practice of desiccation and/or ripening with glyphosate right before the harvest ensures that glyphosate residues are present in our food supply. It is plausible that the recent sharp increase of kidney failure in agricultural workers is tied to glyphosate exposure. We urge governments globally to reexamine their policy towards glyphosate and to introduce new legislation that would restrict its usage.

Acknowledgements

The authors would like to thank Nancy Swanson for her gracious effort in the creation of the informative pictorial graphs included with the text. Her statistical research for glyphosate usage and disease over time is an invaluable contribution to our paper. Stephanie Seneff would also like to personally thank Jennifer Moeny for her most informative discussions concerning current associative prognosis, research and trends in Celiac disease and gluten intolerance. This work was funded in part by Quanta Computers, Taipei, Taiwan, under the auspices of the Qmulus Project.

Disclosures: The authors have nothing to disclose.

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