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OECD approaches and considerations for regulatory evaluation of endocrine disruptors

机译:内分泌破坏者监管评估的经合组织方法和注意事项

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Identifying the potential endocrine disruptor hazard of environmental chemicals is a regulatory mandate for many countries. However, due to the adaptive nature of the endocrine system, absence of a single method capable of identifying endocrine disruption, and the latency between exposure to endocrine disrupting chemical during sensitive life stages and the manifestation of adverse responses, satisfying the regulatory requirement needed to identify a chemical as an endocrine disruptor is a challenge. There are now a variety of validated regulatory tests that can be used in combination to provide evidence that a chemical affects the oestrogen, androgen, thyroid, and steroidogenic pathways of vertebrates, but most rely (at least to some extent) on animal testing and require considerable cost and time to produce the necessary data. Emerging research methods are able to evaluate other endocrine pathways, incorporate more sensitive endpoints, and combine multiple alternative methods to predict in vivo outcomes. Some research approaches may also bridge gaps that have been identified in current endocrine regulatory testing. For the near term, considering new endpoints in a regulatory context may require adding them to existing test methods in order to establish relationships between the traditional and the innovative. From the outset, endocrine testing has always required integration of multiple methods that provide data on different levels of biological organisation, thus, the area of endocrine disruption is particularly adaptable to adverse outcome pathway (AOP) frameworks and integrated test methods built around AOPs. Herein, we provide a review of the status of endocrine disruptors in the OECD context, examples where innovation from research is needed to improve or bridge gaps in endocrine testing, and suggestions for regulators and researchers to facilitate uptake of innovate methods for endocrine disruptor regulatory testing. The increase in several human complex human disorders that include an endocrine component and the alarming decrease in wildlife biodiversity are commanding directives to include the best, most informative, innovative approaches to accelerate the rate and throughput of chemical evaluation for endocrine disruption.
机译:确定环境化学品的潜在内分泌干扰危害是许多国家的监管授权。然而,由于内分泌系统的适应性,不存在能够鉴定内分泌破坏的单一方法,以及暴露于敏感寿命期间的内分泌破坏化学物质的潜伏期和不良反应的表现,满足识别所需的监管要求作为内分泌破坏器的化学品是挑战。现在有各种经过验证的监管测试,可以组合使用,以提供脊椎动物的雌激素,雄激素,甲状腺和类化途径的证据,但最依赖于动物测试和要求产生必要数据的大量成本和时间。新兴的研究方法能够评估其他内分泌途径,包括更敏感的终点,并结合多种替代方法来预测体内结果。一些研究方法还可以在目前的内分泌调节测试中识别出来的差距。对于近期,考虑到监管环境中的新终点可能需要将它们添加到现有的测试方法中,以便在传统和创新之间建立关系。从一开始,内分泌测试始终需要提供多种方法的集成,这些方法提供不同水平的生物组织的数据,因此,内分泌破坏的面积特别适应在AOP周围构建的不利结果途径(AOP)框架和集成测试方法。在此,我们提供了对经合组织背景中内分泌干扰者的状态的审查,其中需要改进或桥接内分泌测试中的缺席或弥补内分泌测试中的缺口,以及监管机构和研究人员的建议,以促进对内分泌干扰监管检测的创新方法的建议。几种人类复杂人类疾病的增加包括内分泌组件和野生动物生物多样性的惊人减少,指挥指令包括最佳,最具信息丰富的创新方法,以加速内分泌中断的化学评价的速率和吞吐量。

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