Global Regulatory Science, Bayer Crop Science, Chesterfield, MO, USA.
Pest Manag Sci. 2020 Sep;76(9):2886-2906. doi: 10.1002/ps.5983. Epub 2020 Jul 17.
Glyphosate was recently evaluated for its potential to interact with the estrogen, androgen and thyroid (EAT) hormone pathways, including steroidogenesis, under the United States Environmental Protection Agency's (USEPA) Endocrine Disruptor Screening Program (EDSP), then by Germany, the rapporteur Member State who led the European Annex 1 renewal for glyphosate, and then by the European Food Protection Agency (EFSA) also as part of the Annex 1 renewal for glyphosate. Under the EDSP, 11 Tier 1 assays were run following the USEPA's validated 890-series test guidelines and included five in vitro and six in vivo assays to evaluate the EAT pathways. Steroidogenesis was evaluated as part of the estrogen and androgen pathways. An up-to-date critical review has been conducted that considered results from the EDSP Tier 1 battery, guideline regulatory studies and an in-depth analysis of the literature studies that informed an endocrine assessment. A strength of this evaluation was that it included data across multiple levels of biological organization, and mammalian and nonmammalian test systems. There was strong agreement across the in vitro and in vivo Tier 1 battery, guideline studies and relevant literature studies, demonstrating that glyphosate does not interact with EAT pathways including steroidogenesis. Based on an analysis of the comprehensive toxicology database for glyphosate and the literature, this review has concluded that glyphosate does not have endocrine-disrupting properties through estrogen, androgen, thyroid and steroidogenic modes of action. © 2020 Society of Chemical Industry.
草甘膦最近在美国环境保护署(USEPA)内分泌干扰物筛选计划(EDSP)下,根据德国的提议,作为对草甘膦的欧盟附件 1 续展的一部分,以及欧洲食品安全局(EFSA)的要求,进行了评估,以确定其是否有可能与雌激素、雄激素和甲状腺(EAT)激素途径相互作用,包括类固醇生成,在德国,作为对草甘膦的欧盟附件 1 续展的报告成员国,领导了这一评估。在 EDSP 下,根据 USEPA 验证的 890 系列测试指南进行了 11 项一级测试,其中包括 5 项体外和 6 项体内测试,以评估 EAT 途径。类固醇生成是雌激素和雄激素途径的一部分。进行了一次最新的批判性审查,考虑了 EDSP 一级电池、指导方针监管研究和内分泌评估所依据的文献研究的结果。这项评估的一个优点是它包括了多个层次的生物学组织、哺乳动物和非哺乳动物测试系统的数据。在体外和体内一级电池、指导方针研究和相关文献研究中都有强烈的一致性,表明草甘膦不会与 EAT 途径相互作用,包括类固醇生成。基于对草甘膦全面毒理学数据库和文献的分析,本综述得出结论,草甘膦通过雌激素、雄激素、甲状腺和类固醇生成作用模式没有内分泌干扰特性。© 2020 化学工业协会。