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Sirtuin 3:心血管疾病治疗的新兴靶点。

Sirtuin 3: Emerging therapeutic target for cardiovascular diseases.

机构信息

Department of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, 212000, China.

Department of Cardiology, Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, 212000, China.

出版信息

Free Radic Biol Med. 2022 Feb 20;180:63-74. doi: 10.1016/j.freeradbiomed.2022.01.005. Epub 2022 Jan 11.

Abstract

Acetylation is one of the most important methods of modification that lead to a change in the function of proteins. In humans, metabolic enzymes commonly undergo acetylation, which regulates the activities of metabolic enzymes and metabolic pathways. Sirtuin 3 (SIRT3) is a prominent deacetylase that participates in mitochondrial metabolism, redox balance, and mitochondrial dynamics by regulating mitochondrial protein acetylation, thereby protecting mitochondria from damage. Normal mitochondrial function is essential for maintaining the metabolism and function of the heart. Therefore, mitochondrial dysfunction caused by SIRT3 consumption and defects leads to the development of a variety of cardiovascular diseases. A comprehensive understanding of the role of SIRT3 in cardiovascular disease is critical for developing new therapeutic strategies. Herein, we summarize the function of SIRT3 in mitochondria, the complex mechanisms mediating cardiovascular diseases, and the potential value of SIRT3 small-molecule agonists in future clinical treatments.

摘要

乙酰化是导致蛋白质功能改变的最重要的修饰方法之一。在人类中,代谢酶通常会发生乙酰化,这调节了代谢酶和代谢途径的活性。Sirtuin 3(SIRT3)是一种重要的去乙酰化酶,通过调节线粒体蛋白乙酰化参与线粒体代谢、氧化还原平衡和线粒体动力学,从而保护线粒体免受损伤。正常的线粒体功能对于维持心脏的代谢和功能至关重要。因此,SIRT3 消耗和缺陷引起的线粒体功能障碍导致多种心血管疾病的发展。全面了解 SIRT3 在心血管疾病中的作用对于开发新的治疗策略至关重要。本文总结了 SIRT3 在线粒体中的功能、介导心血管疾病的复杂机制以及 SIRT3 小分子激动剂在未来临床治疗中的潜在价值。

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