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基于假设的证据权重分析评估全氟己酸的潜在内分泌干扰活性。

A hypothesis-driven weight-of-evidence analysis to evaluate potential endocrine activity of perfluorohexanoic acid.

机构信息

ToxStrategies, Cary, NC, USA.

ToxStrategies, Katy, TX, USA.

出版信息

Regul Toxicol Pharmacol. 2018 Nov;99:168-181. doi: 10.1016/j.yrtph.2018.09.001. Epub 2018 Sep 18.

DOI:10.1016/j.yrtph.2018.09.001
PMID:30240830
Abstract

Perfluorohexanoic acid (PFHxA) is a potential impurity and environmental degradation product of C6-based fluorotelomer products. Considering the potential endocrine activity of perfluoroalkyl acids, a hypothesis-driven weight-of-evidence (WoE) analysis was conducted to evaluate the potential endocrine disruptor activity of PFHxA, as defined by World Health Organization (WHO), across estrogen (E), androgen (A), thyroid (T), and steroidogenesis (S) pathways. A comprehensive literature search identified primary and secondary studies across species for review. The ToxCast/Tox21 database provided in vitro data. Studies identified were reviewed for reliability, and relevance, with endocrine endpoints ranked, and lines of evidence evaluated across pathways. Overall, PFHxA showed no endocrine effects in Japanese medaka, juvenile rainbow trout, chickens or reproductive parameters in northern bobwhite with no significant activity in rodent repeated-dose toxicity, lifetime cancer, or reproductive and developmental studies. In vitro, there was weak or negative activity for T transport protein or activation of E, A or T receptors. PFHxA was also negative in vitro and in vivo for disrupting steroidogenesis. Based on this WoE endocrine analysis, PFHxA exposure did not cause adverse effects associated with alterations in endocrine activity in these models, as such would not be characterized as an endocrine disruptor according to the WHO definition.

摘要

全氟己酸(PFHxA)是基于 C6 的氟调聚物产品的潜在杂质和环境降解产物。考虑到全氟烷基酸的潜在内分泌活性,进行了基于假设的证据权重(WoE)分析,以评估世界卫生组织(WHO)定义的 PFHxA 在雌激素(E)、雄激素(A)、甲状腺(T)和类固醇生成(S)途径中的潜在内分泌干扰物活性。全面的文献检索确定了跨物种的主要和次要研究以供审查。ToxCast/Tox21 数据库提供了体外数据。对研究进行了可靠性和相关性审查,对内分泌终点进行了排序,并对途径中的证据进行了评估。总体而言,PFHxA 在日本青鳉、幼年虹鳟鱼、鸡或北方鹌鹑的生殖参数中没有表现出内分泌效应,在啮齿动物重复剂量毒性、终生癌症或生殖和发育研究中也没有显著活性。在体外,T 转运蛋白或 E、A 或 T 受体的激活呈弱或阴性活性。PFHxA 在体外和体内也没有干扰类固醇生成的作用。基于这种 WoE 内分泌分析,PFHxA 暴露不会导致这些模型中与内分泌活性改变相关的不良影响,因此根据 WHO 的定义,不会被定性为内分泌干扰物。

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