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干扰女性青春期启动的疑似不良结局途径网络,以改善内分泌干扰化学物质的测试和监管。

A Putative Adverse Outcome Pathway Network for Disrupted Female Pubertal Onset to Improve Testing and Regulation of Endocrine Disrupting Chemicals.

机构信息

Neuroendocrinology Unit, GIGA Neurosciences, University of Liège, Liège, Belgium.

Division of Diet, Disease Prevention and Toxicology, National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.

出版信息

Neuroendocrinology. 2022;112(2):101-114. doi: 10.1159/000515478. Epub 2021 Feb 26.

DOI:10.1159/000515478
PMID:33640887
Abstract

The average age for pubertal onset in girls has declined over recent decades. Epidemiological studies in humans and experimental studies in animals suggest a causal role for endocrine disrupting chemicals (EDCs) that are present in our environment. Of concern, current testing and screening regimens are inadequate in identifying EDCs that may affect pubertal maturation, not least because they do not consider early-life exposure. Also, the causal relationship between EDC exposure and pubertal timing is still a matter of debate. To address this issue, we have used current knowledge to elaborate a network of putative adverse outcome pathways (pAOPs) to identify how chemicals can affect pubertal onset. By using the AOP framework, we highlight current gaps in mechanistic understanding that need to be addressed and simultaneously point towards events causative of pubertal disturbance that could be exploited for alternative test methods. We propose 6 pAOPs that could explain the disruption of pubertal timing by interfering with the central hypothalamic trigger of puberty, GnRH neurons, and by so doing highlight specific modes of action that could be targeted for alternative test method development.

摘要

近年来,女孩青春期开始的平均年龄有所下降。人类流行病学研究和动物实验研究表明,环境中存在的内分泌干扰化学物质(EDCs)可能起因果作用。值得关注的是,目前的测试和筛选方案不足以识别可能影响青春期成熟的 EDC,尤其是因为它们没有考虑到生命早期的暴露。此外,EDC 暴露与青春期时间的因果关系仍然存在争议。为了解决这个问题,我们利用现有知识详细阐述了一个假定的不良结局途径(pAOP)网络,以确定化学物质如何影响青春期开始。通过使用 AOP 框架,我们强调了目前在机制理解方面存在的差距,需要加以解决,同时指出可能导致青春期紊乱的事件,这些事件可用于替代测试方法。我们提出了 6 个 pAOP,这些途径可能通过干扰青春期的中枢下丘脑触发 GnRH 神经元来解释青春期时间的扰乱,并突出可能作为替代测试方法开发目标的特定作用模式。

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