Department of Medical Biochemistry, Graduate School of Medicine, Tohoku University, 2-1 Seiryo-machi, Aoba, Sendai, 980-8575, Japan.
Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N, Seattle, WA, 98109, USA.
Arch Pharm Res. 2020 Mar;43(3):337-349. doi: 10.1007/s12272-019-01192-3. Epub 2019 Nov 28.
Liver plays essential roles in the metabolism of many endogenous chemicals and exogenous toxicants. Mechanistic studies in liver have been at the forefront of efforts to probe the roles of bioactivation and detoxication of environmental toxins and toxicants in hepatotoxicity. Moreover, idiosyncratic hepatoxicity remains a key barrier in the clinical development of drugs. The now vast Nrf2 field emerged in part from biochemical and molecular studies on chemical inducers of hepatic detoxication enzymes and subsequent characterization of the modulation of drug/toxicant induced hepatotoxicities in mice through disruption of either Nrf2 or Keap1 genes. In general, loss of Nrf2 increases the sensitivity to such toxic chemicals, highlighting a central role of this transcription factor and its downstream target genes as a modifier to chemical stress. In this review, we summarize the impact of Nrf2 on the toxicology of multiple hepatotoxicants, and discuss efforts to utilize the Nrf2 response in predictive toxicology.
肝脏在许多内源性化学物质和外源性毒物的代谢中发挥着重要作用。肝脏的机制研究一直处于探索环境毒素和毒物的生物活化和解毒作用以及肝毒性作用的前沿。此外,药物的特发性肝毒性仍然是临床开发的一个关键障碍。现在庞大的 Nrf2 领域部分源于对肝解毒酶的化学诱导物的生化和分子研究,以及通过破坏 Nrf2 或 Keap1 基因来随后表征对药物/毒物诱导的肝毒性的调节。一般来说,Nrf2 的缺失会增加对这些有毒化学物质的敏感性,突出了该转录因子及其下游靶基因作为化学应激调节剂的核心作用。在这篇综述中,我们总结了 Nrf2 对多种肝毒物毒理学的影响,并讨论了利用 Nrf2 反应进行预测毒理学的努力。