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机遇危害:NADPH 氧化酶作为心血管疾病治疗靶点的未来。

Opportunity nox: the future of NADPH oxidases as therapeutic targets in cardiovascular disease.

机构信息

Departments of Anatomy and Cell Biology, Free Radical and Radiation Biology, and Internal Medicine, University of Iowa, Iowa City, IA 52242, USA.

出版信息

Cardiovasc Ther. 2013 Jun;31(3):125-37. doi: 10.1111/j.1755-5922.2011.00310.x. Epub 2012 Jan 26.

Abstract

Over 40 years ago, NADPH (nicotinamide adenine dinucleotide phosphate) oxidase 2 (Nox2) was discovered in phagocytes and found to be essential in innate immunity. More than 20 years passed before additional Nox isoforms were discovered; and since then, studies have revealed that several of these isoforms (Nox1, Nox2, Nox4, and Nox5) are found in human cardiac and vascular cells and contribute to the pathogenesis of cardiovascular diseases (CVDs). Recently, major efforts have focused on identifying inhibitors capable of ameliorating Nox-mediated CVD. In this review, we briefly discuss the role of each Nox isoform in CVD, identify steps in Nox signaling that will serve as potential targets for the design of therapeutics, and highlight innovative strategies likely to yield effective Nox inhibitors within the next decade.

摘要

40 多年前,NADPH(烟酰胺腺嘌呤二核苷酸磷酸)氧化酶 2(Nox2)在吞噬细胞中被发现,并且被发现对于先天免疫至关重要。在发现其他 Nox 同工型之前又过去了 20 多年;从那时起,研究表明这些同工型中的几种(Nox1、Nox2、Nox4 和 Nox5)存在于人类心脏和血管细胞中,并导致心血管疾病(CVD)的发病机制。最近,主要的努力集中在识别能够改善 Nox 介导的 CVD 的抑制剂上。在这篇综述中,我们简要讨论了每种 Nox 同工型在 CVD 中的作用,确定了 Nox 信号传递的步骤,这些步骤将作为治疗剂设计的潜在靶点,并强调了在未来十年内可能产生有效 Nox 抑制剂的创新策略。

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