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他汀类药物通过调节Nrf2和Nrf2/HO-1信号通路在不同疾病中的抗氧化作用

Antioxidant Effects of Statins by Modulating Nrf2 and Nrf2/HO-1 Signaling in Different Diseases.

作者信息

Mansouri Atena, Reiner Željko, Ruscica Massimiliano, Tedeschi-Reiner Eugenia, Radbakhsh Shabnam, Bagheri Ekta Mariam, Sahebkar Amirhossein

机构信息

Cellular and Molecular Research Center, Birjand University of Medical Sciences, Birjand 9717853577, Iran.

Biotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad 9177948954, Iran.

出版信息

J Clin Med. 2022 Feb 27;11(5):1313. doi: 10.3390/jcm11051313.

Abstract

Statins are competitive inhibitors of hydroxymethylglutaryl-CoA (HMG-CoA) reductase and have been used to treat elevated low-density lipoprotein cholesterol (LDL-C) for almost four decades. Antioxidant and anti-inflammatory properties which are independent of the lipid-lowering effects of statins, i.e., their pleiotropic effects, might be beneficial in the prevention or treatment of many diseases. This review discusses the antioxidant effects of statins achieved by modulating the nuclear factor erythroid 2 related factor 2/ heme oxygenase-1 (Nrf2/HO-1) pathway in different organs and diseases. Nrf2 and other proteins involved in the Nrf2/HO-1 signaling pathway have a crucial role in cellular responses to oxidative stress, which is a risk factor for ASCVD. Statins can significantly increase the DNA-binding activity of Nrf2 and induce the expression of its target genes, such as HO-1 and glutathione peroxidase) GPx, (thus protecting the cells against oxidative stress. Antioxidant and anti-inflammatory properties of statins, which are independent of their lipid-lowering effects, could be partly explained by the modulation of the Nrf2/HO-1 pathway.

摘要

他汀类药物是羟甲基戊二酰辅酶A(HMG-CoA)还原酶的竞争性抑制剂,已用于治疗低密度脂蛋白胆固醇(LDL-C)升高近四十年。他汀类药物具有独立于其降脂作用的抗氧化和抗炎特性,即其多效性作用,可能对许多疾病的预防或治疗有益。本综述讨论了他汀类药物通过调节不同器官和疾病中的核因子红细胞2相关因子2/血红素加氧酶-1(Nrf2/HO-1)途径所实现的抗氧化作用。Nrf2和参与Nrf2/HO-1信号通路的其他蛋白质在细胞对氧化应激的反应中起关键作用,氧化应激是动脉粥样硬化性心血管疾病(ASCVD)的一个危险因素。他汀类药物可显著增加Nrf2的DNA结合活性并诱导其靶基因的表达,如HO-1和谷胱甘肽过氧化物酶(GPx),从而保护细胞免受氧化应激。他汀类药物独立于其降脂作用的抗氧化和抗炎特性,可能部分是由Nrf2/HO-1途径的调节来解释的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cc0/8911353/962db3de7891/jcm-11-01313-g001.jpg

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