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Dead Genetically Modified Rats
- The mantra is: "Soy (which kills human male reproductive
cells) is good for you", not to mention Genetically Engineered "foods".
- Most Offspring Died
When Mother Rats
Ate GM Soy
By Jeffrey M. Smith
- Author of Seeds of Deception
- GMWatch.com
10-31-5
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- The Russian scientist planned a simple experiment to see if eating
genetically modified (GM) soy might influence offspring. What she got, however, was an
astounding result that may threaten a multi-billion dollar industry.
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- Irina Ermakova, a leading scientist at the Institute of Higher Nervous
Activity and Neurophysiology of the Russian Academy of Sciences (RAS), added GM soy flour
(5-7 grams) to the diet of female rats. Other females were fed non-GM soy or no soy at
all. The experimental diet began two weeks before the rats conceived and continued through
pregnancy and nursing.
-
- Ermakova's first surprise came when her pregnant rats started giving
birth. Some pups from GM-fed mothers were quite a bit smaller. After 2 weeks, 36% of them
weighed less than 20 grams compared to about 6% from the other groups (see photo below).
-
-
- (Photo of two rats from the Russian study, showing stunted growth - the
larger rat, 19 days old, is from the control group; the smaller rat, 20 days old, is from
the "GM soy" group.)
-
- But the real shock came when the rats started dying. Within three weeks,
25 of the 45 (55.6%) rats from the GM soy group died compared to only 3 of 33 (9%) from
the non-GM soy group and 3 of 44 (6.8%) from the non-soy controls.
-
- Ermakova preserved several major organs from the mother rats and
offspring, drew up designs for a detailed organ analysis, created plans to repeat and
expand the feeding trial, and promptly ran out of research money. The $70,000 needed was
not expected to arrive for a year. Therefore, when she was invited to present her research
at a symposium organized by the National Association for Genetic Security, Ermakova wrote
"PRELIMINARY STUDIES" on the top of her paper. She presented it on October 10,
2005 at a session devoted to the risks of GM food.
-
- Her findings are hardly welcome by an industry already steeped in
controversy.
-
- GM Soy's Divisive Past
-
- The soy she was testing was Monsanto's Roundup Ready variety. Its DNA
has bacterial genes added that allow the soy plant to survive applications of Monsanto's
"Roundup" brand herbicide. About 85% of the soy gown in the US is Roundup Ready.
Since soy derivatives, including oil, flour and lecithin, are found in the majority of
processed foods sold in the US, many Americans eat ingredients derived from Roundup Ready
soy everyday.
-
- The FDA does not require any safety tests on genetically modified foods.
If Monsanto or other biotech companies declare their foods safe, the agency has no further
questions. The rationale for this hands-off position is a sentence in the FDA's 1992
policy that states, "The agency is not aware of any information showing that foods
derived by these new methods differ from other foods in any meaningful or uniform
way."[1] The statement, it turns out, was deceptive. Documents made public from a
lawsuit years later revealed that the FDA's own experts agreed that GM foods are different
and might lead to hard-to-detect allergens, toxins, new diseases or nutritional problems.
They had urged their superiors to require long-term safety studies, but were ignored. The
person in charge of FDA policy was, conveniently, Monsanto's former attorney (and later
their vice president). One FDA microbiologist described the GM food policy as "just a
political document" without scientific basis, and warned that industry would
"not do the tests that they would normally do" since the FDA didn't require
any.[2] He was correct.
-
- There have been less than 20 published, peer-reviewed animal feeding
safety studies and no human clinical trials - in spite of the fact that millions of people
eat GM soy, corn, cotton, or canola daily. There are no adequate tests on
"biochemistry, immunology, tissue pathology, gut function, liver function and kidney
function,"[3] and animal feeding studies are too short to adequately test for cancer,
reproductive problems, or effects in the next generation. This makes Ermakova's research
particularly significant. It's the first of its kind.
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- Past Studies Show Significant Effects
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- Other studies on Roundup Ready soy also raise serious questions.
Research on the liver, the body's major de-toxifier, showed that rats fed GM soy developed
misshapen nuclei and other cellular anomalies.[4] This indicates increased metabolic
activity, probably resulting from a major insult to that organ. Rats also showed changes
in the pancreas, including a huge drop in the production of a major enzyme
(alpha-amylase),[5] which could inhibit digestion. Cooked GM soy contains about twice the
amount of soy lectin, which can also block nutrient assimilation.[6] And one study showed
that GM soy has 12-14% less isoflavones, which are touted as cancer fighting.[7]
-
- An animal feeding study published by Monsanto showed no apparent
problems with GM soy,[8] but their research has been severely criticized as rigged to
avoid finding problems.[9] Monsanto used mature animals instead of young, more sensitive
ones, diluted their GM soy up to 12-fold, used too much protein, never weighed the organs,
and had huge variations in starting weights. The study's nutrient comparison between GM
and non-GM soy revealed significant differences in the ash, fat, and carbohydrate content,
lower levels of protein, a fatty acid, and phenylalanine. Monsanto researchers had
actually omitted the most incriminating nutritional differences, which were later
discovered and made public. For example, the published paper showed a 27% increase in a
known allergen, trypsin inhibitor, while the recovered data raised that to a 3-fold or
7-fold increase, after the soy was cooked. This might explain why soy allergies in the UK
skyrocketed by 50% soon after GM soy was introduced.
-
- The gene that is inserted into GM soy produces a protein with two
sections that are identical to known allergens. This might also account for the increased
allergy rate. Furthermore, the only human feeding trial ever conducted confirmed that this
inserted gene transfers into the DNA of bacteria inside the intestines. This means that
long after you decide to stop eating GM soy, your own gut bacteria may still be producing
this potentially allergenic protein inside your digestive tract.
-
- The migration of genes might influence offspring. German scientists
found fragments of the DNA fed to pregnant mice in the brains of their newborn.[10]
Fragments of genetically modified DNA were also found in the blood, spleen, liver and
kidneys of piglets that were fed GM corn.[11] It was not clear if the GM genes actually
entered the DNA of the animal, but scientists speculate that if it were to integrate into
the sex organ cells, it might impact offspring.
-
- The health of newborns might also be affected by toxins, allergens, or
anti-nutrients in the mother's diet. These may be created in GM crops, due to
unpredictable alterations in their DNA. The process of gene insertion can delete one or
more of the DNA's own natural genes, scramble them, turn them off, or permanently turn
them on. It can also change the _expression levels of hundreds of genes. And growing the
transformed cell into a GM plant through a process called tissue culture can create
hundreds or thousands of additional mutations throughout the DNA.
-
- Most of these possibilities have not been properly evaluated in Roundup
Ready soy. We don't know how many mutations or altered gene expressions are found in its
DNA. Years after it was marketed, however, scientists did discover a section of natural
soy DNA that was scrambled[12] and two additional fragments of the foreign gene that had
escaped Monsanto's detection.
-
- Those familiar with the body of GM safety studies are often astounded by
their superficiality. Moreover, several scientists who discovered incriminating evidence
or even expressed concerns about the technology have been fired, threatened, stripped of
responsibilities, or censured.[13] And when problems do arise, they are not followed up.
For example, animals fed GM crops developed potentially precancerous cell growth, smaller
brains, livers and testicles, damaged immune systems, bigger livers, partial atrophy of
the liver, lesions in the livers, stomachs, and kidneys, inflammation of the kidneys,
problems with their blood cells, higher blood sugar levels, and unexplained increases in
the death rate. (See Spilling the Beans, August 2004.) None have been adequately
followed-up or accounted for.
-
- Ermakova's research, however, will likely change that. That's because
her study is easy to repeat and its results are so extreme. A 55.6% mortality rate is
enormous and very worrisome. Repeating the study is the only reasonable option.
-
- American Academy of Environmental Medicine Urges NIH to Follow Up Study
-
- I presented Dr. Ermakova's findings, with her permission, at the annual
conference of the American Academy of Environmental Medicine (AAEM) in Tucson on October
27, 2005. In response, the AAEM board passed a resolution asking the US National
Institutes of Health (NIH) to sponsor an immediate, independent follow-up of the study.
Dr. Jim Willoughby, the Academy's president, said, "Genetically modified soy, corn,
canola, and cottonseed oil are being consumed daily by a significant proportion of our
population. We need rigorous, independent and long-term studies to evaluate if these foods
put the population at risk."
-
- Unfortunately, there is a feature about GM crops that makes even
follow-up studies a problem. In 2003, a French laboratory analyzed the inserted genes in
five GM varieties, including Roundup Ready soybeans.[14] In each case, the genetic
sequence was different than that which had been described by the biotech companies years
earlier. Had all the companies made a mistake? That's unlikely. Rather, the inserted genes
probably rearranged over time. A Brussels lab confirmed that the genetic sequences were
different than what was originally listed. But the sequences discovered in Brussels didn't
all match those found by the French.[15] This suggests that the inserted genes are
unstable and can change in different ways. It also means that they are creating new
proteins-ones that were never intended or tested. The Roundup Ready soybeans used in the
Russian test may therefore be quite different from the Roundup Ready soybeans used in
follow-up studies.
-
- Unstable genes make accurate safety testing impossible. It also may
explain some of the many problems reported about GM foods. For example, nearly 25 farmers
in the US and Canada say that certain GM corn varieties caused their pigs to become
sterile, have false pregnancies, or give birth to bags of water. A farmer in Germany
claims that a certain variety of GM corn killed 12 of his cows and caused others to fall
sick. And Filipinos living next to a GM cornfield developed skin, respiratory, and
intestinal symptoms and fever, while the corn was pollinating. The mysterious symptoms
returned the following year, also during pollination, and blood tests on 39 of the
Filipinos showed an immune response to the Bt toxin-created by the GM corn.
-
- These problems may be due to particular GM varieties, or they may result
from a GM crop that has "gone bad" due to genetic rearrangements. Even GM plants
with identical gene sequences, however, might act differently. The amount of Bt toxin in
the Philippine corn study described above, for example, varied considerably from kernel to
kernel, even in the same plant.[16]
-
- With billions of dollars invested in GM foods, no adverse finding has
yet been sufficient to reverse the industry's growth in the US. It may take some dramatic,
indisputable, and life-threatening discovery. That is why Ermakova's findings are so
important. If the study holds up, it may topple the GM food industry.
-
- I urge the NIH to agree to the AAEM's request, and fund an immediate,
independent follow-up study. If NIH funding is not forthcoming, our Institute for
Responsible Technology will try to raise the money. This is not the time to wait. There is
too much at stake.
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- Click here for press release on Russian rat study.
-
- Click here for the resolution by the American Academy of
Environmental Medicine.
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- Click here for downloadable photos of the rats.
-
-
- Jeffrey M. Smith is working with a team of international scientists to
catalog all known health risks of GM foods. He is the author of Seeds of Deception , the
world's bestselling book on GM food, and the producer of the video, Hidden Dangers in
Kids' Meals.
-
- _____
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- Spilling the Beans is a monthly column available at www.responsibletechnology.org. Publishers and webmasters may offer
this article or monthly series to your readers at no charge, by emailing column@responsibletechnology.org. Individuals may read the column each
month by subscribing to a free newsletter at www.responsibletechnology.org.
-
- _____
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- [1]"Statement of Policy: Foods Derived from New Plant
Varieties," Federal Register vol. 57, no. 104 at 22991, May 29, 1992
- [2]Louis J. Pribyl, "Biotechnology Draft Document, 2/27/92,"
March 6, 1992, www.biointegrity.org
- [3]Epidemiologist Judy Carman's testimony before New Zealand's Royal
Commission of Inquiry on Genetic Modification, 2001.
- [4]Malatesta M, Caporaloni C, Gavaudan S, Rocchi MB, Serafini S, Tiberi
C, Gazzanelli G. (2002a) Ultrastructural morphometrical and immunocytochemical analyses of
hepatocyte nuclei from mice fed on genetically modified soybean. Cell Struct Funct. 27:
173-180.
- [5]Manuela Malatesta, et al, Ultrastructural analysis of pancreatic
acinar cells from mice fed on genetically modified soybean, Journal of Anatomy, Volume 201
Issue 5 Page 409 - November 2002
- [6]Stephen R. Padgette and others, "The Composition of
Glyphosate-Tolerant Soybean Seeds Is Equivalent to That of Conventional Soybeans,"
The Journal of Nutrition, vol. 126, no. 4, April 1996 (The data was taken from the journal
archives, as it had been omitted from the published study.)
- [7]Lappe, M.A., Bailey, E.B., Childress, C. and Setchell, K.D.R. (1999)
Alterations in clinically important phytoestrogens in genetically modified,
herbicide-tolerant soybeans. Journal of Medical Food 1, 241-245.
- [8]Stephen R. Padgette and others, "The Composition of
Glyphosate-Tolerant Soybean Seeds Is Equivalent to That of Conventional Soybeans,"
The Journal of Nutrition, vol. 126, no. 4, April 1996
- [9]For example, Ian F. Pryme and Rolf Lembcke, "In Vivo Studies on
Possible Health Consequences of genetically modified food and Feed-with Particular Regard
to Ingredients Consisting of Genetically Modified Plant Materials," Nutrition and
Health, vol. 17, 2003
- [10]Doerfler W; Schubbert R, "Uptake of foreign DNA from the
environment: the gastrointestinal tract and the placenta as portals of entry,"
Journal of molecular genetics and genetics Vol 242: 495-504, 1994
- [11]Raffaele Mazza1, et al, "Assessing the Transfer of Genetically
Modified DNA from Feed to Animal Tissues," Transgenic Research, October 2005, Volume
14, Number 5, pp 775 - 784
- [12]P. Windels, I. Taverniers, A. Depicker, E. Van Bockstaele, and M.
DeLoose, "Characterisation of the Roundup Ready soybean insert," European Food
Research and Technology, vol. 213, 2001, pp. 107-112
- [13]Jeffrey M. Smith, Seeds of Deception, Yes! Books, 2003
- [14] Collonier C, Berthier G, Boyer F, Duplan M-N, Fernandez S, Kebdani
N, Kobilinsky A, Romanuk M, Bertheau Y. Characterization of commercial GMO inserts: a
source of useful material to study genome fluidity. Poster presented at ICPMB:
International Congress for Plant Molecular Biology (n�VII), Barcelona, 23-28th June 2003.
Poster courtesy of Dr. Gilles-Eric Seralini, Pr�sident du Conseil Scientifique du
CRII-GEN, www.crii-gen.org; also "Transgenic lines proven unstable" by
Mae-Wan Ho, ISIS Report, 23 October 2003 www.i-sis.org.uk
- [15] http://www.i-sis.org.uk/UTLI.php
- [16] http://www.seedsofdeception.com/utility/showArticle/?objectID=36
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- � Copyright 2005 by Jeffrey M. Smith.
- Permission is granted to reproduce this in whole or in part.
-
- http://www.seedsofdeception.com/utility/showArticle/?objectID=297
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