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Nrf2 和 PPAR 激活剂对代谢和药物诱导的氧化损伤的协同作用。

Collaborative Power of Nrf2 and PPAR Activators against Metabolic and Drug-Induced Oxidative Injury.

机构信息

College of Pharmacy, Dongguk University, Goyang 10326, Republic of Korea.

出版信息

Oxid Med Cell Longev. 2017;2017:1378175. doi: 10.1155/2017/1378175. Epub 2017 Aug 27.

Abstract

Mammalian cells have evolved a unique strategy to protect themselves against oxidative damage induced by reactive oxygen species (ROS). Especially, two transcription factors, nuclear factor erythroid 2p45-related factor 2 (Nrf2) and peroxisome proliferator-activated receptor (PPAR), have been shown to play key roles in establishing this cellular antioxidative defense system. Recently, several researchers reported ameliorating effects of pharmacological activators for these Nrf2 and PPAR pathways on the progression of various metabolic disorders and drug-induced organ injuries by oxidative stress. In this review, general features of Nrf2 and PPAR pathways in the context of oxidative protection will be summarized first. Then, a number of successful applications of natural and synthetic Nrf2 and PPAR activators to the alleviation of pathological and drug-related oxidative damage will be discussed later.

摘要

哺乳动物细胞进化出一种独特的策略来保护自己免受活性氧(ROS)诱导的氧化损伤。特别是,两种转录因子,核因子红细胞 2p45 相关因子 2(Nrf2)和过氧化物酶体增殖物激活受体(PPAR),已被证明在建立这种细胞抗氧化防御系统中发挥关键作用。最近,一些研究人员报道了这些 Nrf2 和 PPAR 途径的药理学激活剂对各种代谢紊乱和氧化应激诱导的药物性器官损伤的进展的改善作用。在这篇综述中,首先总结了 Nrf2 和 PPAR 途径在氧化保护方面的一般特征。然后,讨论了一些天然和合成的 Nrf2 和 PPAR 激活剂在减轻病理性和药物相关氧化损伤方面的成功应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e913/5591982/dd61ce601eee/OMCL2017-1378175.001.jpg

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