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基质金属蛋白酶-2的激活是心脏氧化应激损伤中的关键事件。

Activation of MMP-2 as a key event in oxidative stress injury to the heart.

作者信息

Ali Mohammad A M, Schulz Richard

机构信息

Department of Pharmacology, Cardiovascular Research Group, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Front Biosci (Landmark Ed). 2009 Jan 1;14(2):699-716. doi: 10.2741/3274.

Abstract

Oxygen and nitrogen derived free radicals play a crucial role in both cardiac physiology and pathology. In this review we discuss how these molecules interact in the cardiac cell, some aspects of their physiological importance, and their pathological effects with a special focus on the activation of matrix metalloproteinases (MMPs) as an early event in oxidative stress damage. MMPs are a family of zinc-dependent endopeptidases which play an active role in regulating the extracellular matrix. Recently, however, it has been recognized that MMPs may also rapidly act on intracellular substrates on a minutes timescale. This review will consider some recent developments in the intracellular localization and novel substrates of MMP-2 within the heart. In addition, we will discuss MMP inhibition as a novel therapeutic strategy to prevent oxidative stress damage to the heart.

摘要

氧和氮衍生的自由基在心脏生理和病理过程中都起着至关重要的作用。在这篇综述中,我们将讨论这些分子在心脏细胞中的相互作用方式、它们生理重要性的一些方面,以及它们的病理效应,特别关注基质金属蛋白酶(MMPs)的激活作为氧化应激损伤的早期事件。MMPs是一类锌依赖性内肽酶家族,在调节细胞外基质中发挥积极作用。然而,最近人们认识到,MMPs也可能在几分钟的时间尺度上迅速作用于细胞内底物。本综述将探讨心脏内MMP-2细胞内定位和新底物的一些最新进展。此外,我们还将讨论MMP抑制作为预防心脏氧化应激损伤的一种新治疗策略。

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