环境化学物质对线粒体功能障碍的影响

M. Xia
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引用次数: 0

摘要

Tox21项目由美国国立卫生研究院、美国环境保护局和美国食品和药物管理局合作,利用定量高通量筛选(qHTS)方法,通过一系列与生物相关的细胞或生化分析,对成千上万种环境化学物质进行了分析。Tox21筛选产生的数据可用于确定化合物作用机制,优先考虑化学物质进行更广泛的毒理学评估,并建立体内生物反应的预测模型。作为Tox21项目的一部分,我们使用qHTS方法筛选了Tox21 10K化合物抗线粒体膜电位(MMP)测定。从初步筛选(1),一组已知的和新的化学物质(如对羟基苯甲酸酯),降低了MMP已被确定。鉴定出的化合物已经在人和大鼠肝细胞中进行了测试,以测量MMP的变化,线粒体相关的细胞通路,包括p53和Nrf2/ARE,以及线粒体呼吸。这些结果将有助于为进一步深入的基于机制的毒性试验确定化学品的优先次序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Profiling of Environmental Chemicals for Mitochondrial Dysfunction
The Tox21 program, a collaboration of the National Institutes of Health, Environmental Protection Agency, and Food and Drug Administration, has utilized a quantitative high throughput screening (qHTS) approach to profile thousands and thousands of environmental chemicals against a battery of biologically relevant cell- or biochemical-based assays. The data generated from Tox21 screening can be used to identify mechanisms of compound action, prioritize chemicals for more extensive toxicological evaluation, and develop the predictive models of in vivo biological responses. As the part of Tox21 program, we have screened the Tox21 10K compounds against mitochondrial membrane potential (MMP) assay using a qHTS approach. From the primary screening (1), a group of known and novel chemicals (e.g. parabens) that decreased the MMP have been identified. The identified compounds have been tested in the human and rat hepatocytes to measure MMP changes, mitochondria related cellular pathways including p53 and Nrf2/ARE, and mitochondrial respiration. These results will be useful for prioritizing chemicals for further in-depth mechanism-based toxicity testing.
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