de Peyster Ann, Mihaich Ellen
Graduate School of Public Health, San Diego State University, 5500 Campanile Drive, San Diego, CA 92182, United States.
Environmental and Regulatory Resources, LLC, 6807 Lipscomb Drive, Durham, NC 27712, United States.
Regul Toxicol Pharmacol. 2014 Aug;69(3):348-70. doi: 10.1016/j.yrtph.2014.04.017. Epub 2014 May 6.
Endocrine-related endpoints in animals have been reported to respond to high doses of methyl tertiary-butyl ether (MTBE), however, a systematic and transparent evaluation of endocrine potential has not been published. Resolving whether MTBE exhibits endocrine activity is important given regulatory and public interest in endocrine disrupting substances and their potential for causing adverse effects in humans or wildlife. A weight-of-evidence (WoE) analysis was conducted, focusing on hypotheses related to the potential for MTBE to interact with estrogen, androgen, and thyroid pathways, and steroidogenesis. To reach scientifically justified conclusions based on the totality of evidence, this WoE procedure involved a semi-quantitative relevance weighting of each endpoint for each hypothesis and systematic consideration of each endpoint in various study designs. This procedure maximized use of an extensive body of relevant and reliable literature on MTBE with evidence supporting or opposing a given mode of action hypothesis. Evaluating the strength and consistency of observations from many MTBE studies also provided a way to assess whether high doses used in experiments with MTBE confound identification of direct endocrine system responses. Based on results of studies using mammalian and fish models and in vitro screening assays, this WoE assessment reveals that MTBE lacks direct endocrine activity.
据报道,动物体内与内分泌相关的终点指标会对高剂量的甲基叔丁基醚(MTBE)产生反应,然而,尚未发表对其内分泌潜能的系统且透明的评估。鉴于监管机构和公众对内分泌干扰物质及其对人类或野生动物造成不利影响的可能性的关注,确定MTBE是否具有内分泌活性至关重要。进行了证据权重(WoE)分析,重点关注与MTBE与雌激素、雄激素、甲状腺途径以及类固醇生成相互作用的可能性相关的假设。为了基于全部证据得出科学合理的结论,此WoE程序涉及对每个假设的每个终点指标进行半定量相关性加权,并系统考虑各种研究设计中的每个终点指标。该程序最大限度地利用了大量关于MTBE的相关且可靠的文献,这些文献提供了支持或反对给定作用模式假设的证据。评估来自许多MTBE研究的观察结果的强度和一致性,也提供了一种方法来评估在MTBE实验中使用的高剂量是否混淆了直接内分泌系统反应的识别。基于使用哺乳动物和鱼类模型以及体外筛选试验的研究结果,此WoE评估表明MTBE缺乏直接内分泌活性。