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Mode of action frameworks: a critical analysis.

机译:行动模式框架:批判性分析。

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Mode of action (MOA) information is increasingly being applied in human health risk assessment. The MOA can inform issues such as the relevance of observed effects in laboratory animals to humans, and the variability of response within the human population. Several collaborative groups have developed frameworks for analyzing and utilizing MOA information in human health risk assessment of environmental carcinogens and toxins, including the International Programme on Chemical Safety, International Life Sciences Institute, and U.S. Environmental Protection Agency. With the goal of identifying gaps and opportunities for progress, we critically evaluate several of these MOA frameworks. Despite continued improvement in incorporating biological data in human health risk assessment, several notable challenges remain. These include articulation of the significant role of scientific judgment in establishing an MOA and its relevance to humans. In addition, binary (yeso) decisions can inappropriately exclude consideration of data that may nonetheless be informative to the overall assessment of risk. Indeed, the frameworks lack a broad consideration of known causes of human disease and the potential for chemical effects to act additively with these as well as endogenous background processes. No integrated analysis of the impact of multiple MOAs over the same dose range, or of varying MOAs at different life stages, is included. Separate consideration of each MOA and outcome limits understanding of how multiple metabolites, modes, and toxicity pathways contribute to the toxicological profile of the chemical. An extension of the analyses across outcomes with common modes is also needed.
机译:行动模式(MOA)信息越来越多地应用于人类健康风险评估中。 MOA可以告知一些问题,例如实验动物中观察到的效果与人类的相关性以及人群中反应的变异性。几个合作小组已经开发出了用于分析和利用MOA信息进行环境致癌物和毒素的人类健康风险评估的框架,包括国际化学安全计划,国际生命科学研究所和美国环境保护署。为了找出差距和进步机会,我们对这些MOA框架进行了严格评估。尽管在将生物数据纳入人类健康风险评估方面继续取得了进步,但仍存在一些明显的挑战。其中包括阐明科学判断在建立MOA中的重要作用及其与人类的关系。此外,二元(是/否)决策可能会不适当地排除对数据的考虑,而这些数据可能仍有助于整体风险评估。确实,这些框架没有广泛考虑人类疾病的已知原因以及化学效应与这些以及内源性背景过程相加作用的可能性。没有包括对同一剂量范围内多种MOA的影响或不同生命阶段中不同MOA的影响的综合分析。对每种MOA和结果的单独考虑限制了对多种代谢物,模式和毒性途径如何促进化学物质毒理学特性的理解。还需要将分析扩展到具有通用模式的结果。

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