Friday, August 27, 2010

Rounding up the evidence on glyphosate

We've blogged a few times (here, e.g.) about the unintended consequences of the widespread use of genetically modified Roundup-resistant plants and, consequently, Roundup (Roundup is an herbicide, and its active ingredient is glyphosate).  Not surprisingly to anyone except Monsanto--the original producers of the stuff, who said this wouldn't happen--Roundup is encouraging the growth of herbicide-resistant weeds wherever it's liberally used, and thus the need for farmers to use more, and more toxic, herbicides, or more labor-intensive horticultural practices to deal with these newly stubborn weeds.  That's evolution for ya.

But other effects are getting some attention too.  A quick check on Google and Google Scholar provides evidence that for more than a decade there have been anecdotal and scientific journal reports of neural, craniofacial, limb and other anomalies in infants born in regions with intensive Roundup use, as well as effects on amphibians and other vertebrates living in or near the fields.  Any organism exposed to water that contains glyphosate-laced runoff apparently is also at risk.

Among many other reports, a 2009 paper finds that glyphosate alone is toxic to cells, and that other chemicals added to the herbicide, supposedly inert, exacerbate the effect.
We have evaluated the toxicity of four glyphosate (G)-based herbicides in Roundup (R) formulations, from 105 times dilutions, on three different human cell types. This dilution level is far below agricultural recommendations and corresponds to low levels of residues in food or feed. The formulations have been compared to G alone and with its main metabolite AMPA or with one known adjuvant of R formulations, POEA. HUVEC primary neonate umbilical cord vein cells have been tested with 293 embryonic kidney and JEG3 placental cell lines. All R formulations cause total cell death within 24 h, through an inhibition of the mitochondrial succinate dehydrogenase activity, and necrosis, by release of cytosolic adenylate kinase measuring membrane damage. They also induce apoptosis via activation of enzymatic caspases 3/7 activity. 
The real threshold of G toxicity must take into account the presence of adjuvants but also G metabolism and time-amplified effects or bioaccumulation. This should be discussed when analyzing the in vivo toxic actions of R. This work clearly confirms that the adjuvants in Roundup formulations are not inert. Moreover, the proprietary mixtures available on the market could cause cell damage and even death around residual levels to be expected, especially in food and feed derived from R formulation-treated crops.
Now a paper in the journal Chemical Research in Toxicology (Aug 9, 2010) reports the teratogenic effects of incubating frog and chick embryos with a 1/5000 dilution of glyphosate, and suggests a mechanism to explain the effect.
The treated embryos were highly abnormal with marked alterations in cephalic and neural crest development and shortening of the anterior−posterior (A-P) axis. Alterations on neural crest markers were later correlated with deformities in the cranial cartilages at tadpole stages. Embryos injected with pure glyphosate showed very similar phenotypes. Moreover, GBH [glyphosate based herbicides] produced similar effects in chicken embryos, showing a gradual loss of rhombomere domains, reduction of the optic vesicles, and microcephaly......  A reporter gene assay revealed that GBH treatment increased endogenous retinoic acid (RA) activity in Xenopus embryos and cotreatment with a RA antagonist rescued the teratogenic effects of the GBH. Therefore, we conclude that the phenotypes produced by GBH are mainly a consequence of the increase of endogenous retinoid activity..... The direct effect of glyphosate on early mechanisms of morphogenesis in vertebrate embryos opens concerns about the clinical findings from human offspring in populations exposed to GBH in agricultural fields.
Retinoic acid is a signaling factor that is essential for cell differentiation in the developing embryo, as a regulator of major stages in growth and patterning.  If glyphosate is confirmed to interfere with retinoic acid levels in developing vertebrate embryos, as this study suggests, it's a serious problem for farm workers, people who live in regions where glyphosate is used heavily, or who use water from sources contaminated with glyphosate runoff, as well as any other vertebrate exposed to this stuff.

The point here is not to take political sides, but to stress that evaluating the evidence independently, regardless of commercial interest (or, for that matter, tree-hugger interests) is the only way to even have a good chance of preventing major calamities--or, to become confident that they won't occur.  But what we know about evolution and development make it quite conceivable that the problems are real.


Jennifer said...

just for the record, we don't use it so anyone downstream is currently safe. Did you know that farmers have to be licensed to apply that stuff but that regular people can go to the store and get some to apply to their own yards, unregulated? Not just farmers and farm workers needing to be careful

Anne Buchanan said...

Can farmers use only a limited amount per acre or something? What does the licensing involve?

John said...

We all know that this is a completely twisted environment involving stupid patent law, and even stupider patents. There is no sensible justification for these restrictions, especially in light of simple evolutionary science. We always hear: "but if not for the the guarantee of years of exploitative profits, nobody would develop the next ..." First, there is little evidence other than capitalist bias to support that contention, and, second, who the fuck cares? What has this process produced, really, that matters at all for the general public, that would not otherwise have happened, anyway? I want real evidence, not the "but it is as good as aspirin" apologies that we have seen for the past 20 years.