Suppr超能文献

作用机制信息在风险评估中的应用:用于模拟关键事件剂量反应的定量关键事件/剂量反应框架

The use of mode of action information in risk assessment: quantitative key events/dose-response framework for modeling the dose-response for key events.

作者信息

Simon Ted W, Simons S Stoney, Preston R Julian, Boobis Alan R, Cohen Samuel M, Doerrer Nancy G, Fenner-Crisp Penelope A, McMullin Tami S, McQueen Charlene A, Rowlands J Craig

机构信息

Ted Simon LLC , Winston, GA , USA.

出版信息

Crit Rev Toxicol. 2014 Aug;44 Suppl 3:17-43. doi: 10.3109/10408444.2014.931925.

Abstract

The HESI RISK21 project formed the Dose-Response/Mode-of-Action Subteam to develop strategies for using all available data (in vitro, in vivo, and in silico) to advance the next-generation of chemical risk assessments. A goal of the Subteam is to enhance the existing Mode of Action/Human Relevance Framework and Key Events/Dose Response Framework (KEDRF) to make the best use of quantitative dose-response and timing information for Key Events (KEs). The resulting Quantitative Key Events/Dose-Response Framework (Q-KEDRF) provides a structured quantitative approach for systematic examination of the dose-response and timing of KEs resulting from a dose of a bioactive agent that causes a potential adverse outcome. Two concepts are described as aids to increasing the understanding of mode of action-Associative Events and Modulating Factors. These concepts are illustrated in two case studies; 1) cholinesterase inhibition by the pesticide chlorpyrifos, which illustrates the necessity of considering quantitative dose-response information when assessing the effect of a Modulating Factor, that is, enzyme polymorphisms in humans, and 2) estrogen-induced uterotrophic responses in rodents, which demonstrate how quantitative dose-response modeling for KE, the understanding of temporal relationships between KEs and a counterfactual examination of hypothesized KEs can determine whether they are Associative Events or true KEs.

摘要

HESI风险21项目组建了剂量反应/作用模式子团队,以制定策略,利用所有可用数据(体外、体内和计算机模拟数据)推动下一代化学物质风险评估的发展。该子团队的一个目标是完善现有的作用模式/人体相关性框架和关键事件/剂量反应框架(KEDRF),以便充分利用关键事件(KEs)的定量剂量反应和时间信息。由此产生的定量关键事件/剂量反应框架(Q-KEDRF)提供了一种结构化的定量方法,用于系统检查生物活性剂剂量导致潜在不良后果时KEs的剂量反应和时间情况。文中描述了两个有助于增进对作用模式理解的概念——关联事件和调节因素。这两个概念在两个案例研究中得到了说明:1)农药毒死蜱对胆碱酯酶的抑制作用,该案例说明了在评估调节因素(即人类中的酶多态性)的影响时考虑定量剂量反应信息的必要性;2)雌激素诱导的啮齿动物子宫肥大反应,该案例展示了如何对KE进行定量剂量反应建模、理解KE之间的时间关系以及对假设的KE进行反事实检验,从而确定它们是关联事件还是真正的KE。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验