沉默调节蛋白1抑制血管内皮细胞中的氧化应激。

Sirt1 Inhibits Oxidative Stress in Vascular Endothelial Cells.

作者信息

Zhang Weijin, Huang Qiaobing, Zeng Zhenhua, Wu Jie, Zhang Yaoyuan, Chen Zhongqing

机构信息

Department of Critical Care Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Guangdong Key Lab of Shock and Microcirculation Research, Department of Pathophysiology, Southern Medical University, Guangzhou 510515, China.

出版信息

Oxid Med Cell Longev. 2017;2017:7543973. doi: 10.1155/2017/7543973. Epub 2017 May 4.

Abstract

The vascular endothelium is a layer of cells lining the inner surface of vessels, serving as a barrier that mediates microenvironment homeostasis. Deterioration of either the structure or function of endothelial cells (ECs) results in a variety of cardiovascular diseases. Previous studies have shown that reactive oxygen species (ROS) is a key factor that contributes to the impairment of ECs and the subsequent endothelial dysfunction. The longevity regulator Sirt1 is a NAD-dependent deacetylase that has a potential antioxidative stress activity in vascular ECs. The mechanisms underlying the protective effects involve Sirt1/FOXOs, Sirt1/NF-B, Sirt1/NOX, Sirt1/SOD, and Sirt1/eNOs pathways. In this review, we summarize the most recent reports in this field to recapitulate the potent mechanisms involving the protective role of Sirt1 in oxidative stress and to highlight the beneficial effects of Sirt1 on cardiovascular functions.

摘要

血管内皮是一层衬于血管内表面的细胞,作为介导微环境稳态的屏障。内皮细胞(ECs)结构或功能的恶化会导致多种心血管疾病。先前的研究表明,活性氧(ROS)是导致ECs损伤及随后内皮功能障碍的关键因素。长寿调节因子Sirt1是一种NAD依赖性脱乙酰酶,在血管ECs中具有潜在的抗氧化应激活性。其保护作用的潜在机制涉及Sirt1/FOXOs、Sirt1/NF-κB、Sirt1/NOX、Sirt1/SOD和Sirt1/eNOs信号通路。在本综述中,我们总结了该领域的最新报道,以概括Sirt1在氧化应激中的保护作用所涉及的潜在机制,并强调Sirt1对心血管功能的有益影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52d1/5435972/8f598d0f86f9/OMCL2017-7543973.001.jpg

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