Hypothetical adjustment of the acceptable daily intake and correction of the underrated risk: A case study of glyphosate-based herbicides

Y. A. Ibrahim
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引用次数: 5

Abstract

Following the introduction of genetically-engineered glyphosate-resistant (GEGR) crops, commercially known as Roundup Ready (RR), no pesticide’s active principle has been used as much as glyphosate; yet its safety measures have been sternly disputed.  After its classification by the International Agency for Research on Cancer (IARC) as probably carcinogenic to humans in 2015, scientists, activists, regulators and the general public revisited voluminous studies that outweighed the risk of this herbicide and raised ferocious concerns that warranted serious attention.  Recently published studies on glyphosate established at least four toxicological principles. First, glyphosate exhibited severe mammalian toxicity at concentrations orders of magnitude lower than its regulatory-promulgated ‘No Observed Adverse Effect Level’ (NOAEL) or even its ‘Chronic Reference Dose’ (cRfD) and ‘Acceptable Daily Intake’ (ADI).  Second, even though not transparently scrutinized or officially required for toxicological testing and risk assessment, glyphosate co-formulants and glyphosate-based herbicides (GBHs) are orders of magnitude more toxic than the principle active ingredient alone. Third, glyphosate and GBHs are cytotoxic and endocrine disruptors, and the latter explains why ultra low concentrations - yet environmentally relevant-cause severe chronic toxicity. Fourth, the endocrine disruption likely leads to epigenotoxicity that may be extended to offspring and unexposed descending generations.  Taken all together, it can be fairly said that confidence in the regulatory-certified ADI values is highly eroded. To resolve the paradoxical discrepancy between regulatory safety measures and elicited toxicities at concentrations far below these measures, ADI was refined using two safety or adjustment factors.  Together, these two factors scale down ADI by four orders of magnitude and bring it to an Adjusted ADI (AADI) value of 2.5 ng/kg bw/day. Contrary to regulatory ADI, the new AADI successfully explains many research findings which demonsted severe mammalian toxicity at concentrations in the neighborhood of nanograms a.i./kg bw/day. This distills confidence in the new AADI value, as well as the magnitude of the proposed safety factors.  Glyphosate uses as per human capita, in two countries representing the extremes of adopting RR crops (the USA) or not-adopting these crops (Egypt), were compared. The comparison confirms the association between growing RR crops and the escalated use of glyphosate, and shows that the American public is likely exposed to glyphosate residue at forty times higher levels than the Egyptian public.   Key words: Acceptable daily intake, adjuvant, chronic reference dose, co-formulants, food quality protection act, hazard, glyphosate, glyphosate-based herbicides, no observed adverse effect level, risk, roundup, roundup ready crops.
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假设每日可接受摄入量的调整和低估风险的纠正:草甘膦除草剂的案例研究
在引入抗草甘膦(GEGR)转基因作物(商业上称为抗农达(RR))之后,没有任何一种农药的活性原理能像草甘膦那样被大量使用;然而,它的安全措施一直备受争议。2015年,国际癌症研究机构(International Agency for Research on Cancer, IARC)将其列为可能对人类致癌的物质,此后,科学家、活动人士、监管机构和公众重新审视了大量的研究,这些研究超越了这种除草剂的风险,引发了强烈的担忧,值得认真关注。最近发表的关于草甘膦的研究至少确立了四项毒理学原则。首先,草甘膦表现出严重的哺乳动物毒性,其浓度低于监管机构颁布的“无观察到的不良影响水平”(NOAEL),甚至低于其“慢性参考剂量”(cRfD)和“可接受的每日摄入量”(ADI)。其次,即使没有经过透明的审查,也没有正式要求进行毒理学测试和风险评估,草甘膦共制剂和草甘膦除草剂(GBHs)的毒性比主要活性成分单独的毒性要高几个数量级。第三,草甘膦和GBHs具有细胞毒性和内分泌干扰物,后者解释了为什么超低浓度(但与环境相关)会导致严重的慢性毒性。第四,内分泌紊乱可能导致表观遗传毒性,并可能延伸到后代和未暴露的后代。总的来说,可以公平地说,对监管机构认证的ADI值的信心受到了严重的侵蚀。为了解决监管安全措施与远低于这些措施的浓度引起的毒性之间的矛盾差异,ADI使用两个安全或调整因素进行了改进。综上所述,这两个因素将ADI降低了四个数量级,并使其达到2.5 ng/kg bw/day的调整后ADI (AADI)值。与规范的每日推荐摄入量相反,新的每日推荐摄入量成功地解释了许多研究结果,这些研究结果表明,在接近纳克a.i./kg bw/天的浓度下,哺乳动物具有严重的毒性。这使人们对新的AADI值以及所建议的安全系数的大小产生了信心。比较了采用抗草甘膦作物(美国)和不采用抗草甘膦作物(埃及)这两个极端国家的人均草甘膦使用量。这一比较证实了种植抗草甘膦作物与草甘膦使用量增加之间的联系,并表明美国公众接触到的草甘膦残留量可能是埃及公众的40倍。关键词:每日可接受摄入量,佐剂,慢性参考剂量,共制剂,食品质量保护法,危害,草甘膦,草甘膦基除草剂,未观察到的不良影响水平,风险,农达,抗农达作物。
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