Crit Rev Toxicol. 2013 Apr;43(4):283-315. doi: 10.3109/10408444.2013.770820. Epub 2013 Mar 12.
An earlier review of the toxicity of glyphosate and the original Roundup™-branded formulation concluded that neither glyphosate nor the formulation poses a risk for the production of heritable/somatic mutations in humans. The present review of subsequent genotoxicity publications and regulatory studies of glyphosate and glyphosate-based formulations (GBFs) incorporates all of the findings into a weight of evidence for genotoxicity. An overwhelming preponderance of negative results in well-conducted bacterial reversion and in vivo mammalian micronucleus and chromosomal aberration assays indicates that glyphosate and typical GBFs are not genotoxic in these core assays. Negative results for in vitro gene mutation and a majority of negative results for chromosomal effect assays in mammalian cells add to the weight of evidence that glyphosate is not typically genotoxic for these endpoints in mammalian systems. Mixed results were observed for micronucleus assays of GBFs in non-mammalian systems. Reports of positive results for DNA damage endpoints indicate that glyphosate and GBFs tend to elicit DNA damage effects at high or toxic dose levels, but the data suggest that this is due to cytotoxicity rather than DNA interaction with GBF activity perhaps associated with the surfactants present in many GBFs. Glyphosate and typical GBFs do not appear to present significant genotoxic risk under normal conditions of human or environmental exposures.
先前对草甘膦毒性的审查以及对原始的 Roundup™品牌制剂的审查得出结论,草甘膦和制剂都不会对人类遗传/体细胞突变的产生构成风险。本审查对随后的草甘膦和基于草甘膦的制剂(GBF)的遗传毒性出版物和监管研究进行了综合评估,将所有发现纳入遗传毒性的证据权重中。大量良好设计的细菌回复、体内哺乳动物微核和染色体畸变检测的阴性结果表明,草甘膦和典型的 GBF 在这些核心检测中没有遗传毒性。体外基因突变检测的阴性结果和哺乳动物细胞中染色体效应检测的大多数阴性结果进一步证明,草甘膦在哺乳动物系统中对于这些终点通常没有遗传毒性。GBF 的非哺乳动物系统中的微核检测结果存在混合结果。DNA 损伤终点阳性结果的报告表明,草甘膦和 GBF 往往在高剂量或毒性剂量水平下引起 DNA 损伤效应,但数据表明这是由于细胞毒性而不是 DNA 与 GBF 活性的相互作用所致,这种相互作用可能与许多 GBF 中存在的表面活性剂有关。在人类或环境暴露的正常条件下,草甘膦和典型的 GBF 似乎不会带来重大的遗传毒性风险。