综述

补体C1q肿瘤坏死因子相关蛋白7在心血管代谢性疾病中的作用及机制

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  • (1 武汉体育学院运动医学院,武汉430070; 2运动训练监控湖北省重点实验室,武汉430070)

收稿日期: 2023-04-11

  修回日期: 2023-05-06

  录用日期: 2023-05-09

  网络出版日期: 2024-04-25

基金资助

2022年教育部人文社会科学基金(22YJCZH138);武汉体育学院中青年科研团队(21KT11)资助课题

Roles and Mechanisms of Complement C1q TNF-Related Protein 7 in Cardiometabolic Disease

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  • (1Department of Sports Medicine, Wuhan Sports University, Wuhan 430070, China; 2Hubei Key Laboratory of Sports Training Monitoring, Wuhan 430070, China)

Received date: 2023-04-11

  Revised date: 2023-05-06

  Accepted date: 2023-05-09

  Online published: 2024-04-25

摘要

心血管代谢性疾病(cardiometabolic disease,CMD)是指代谢系统和心血管系统单一或者同时发生、可相互影响的病理改变,是代谢性疾病和心血管疾病的总称。包括肥胖、胰岛素抵抗、代谢综合征、糖尿病以及冠心病等。脂肪因子在CMD 的发生发展中发挥关键性作用。补体C1q肿瘤坏死因子相关蛋白7(complement C1q TNF-related protein 7,CTRP7)是新近发现的脂肪因子,与肥胖、糖尿病及冠心病等CMD密切相关。本文围绕CTRP7生物学特性,综述其在CMD(包括肥胖、2型糖尿病和冠心病)发生发展中的作用,及可能的作用机制如多种途径调控糖脂代谢、降低胰岛素敏感性、促进炎症反应和增加氧化应激等,以期为CTRP7作为CMD 的治疗靶标提供依据和参考。

本文引用格式

李定微1, 钱帅伟1, 2, 李春艳1, 2, △ . 补体C1q肿瘤坏死因子相关蛋白7在心血管代谢性疾病中的作用及机制[J]. 生理科学进展, 2024 , 55(2) : 126 -132 . DOI: 10.20059/j.cnki.pps.2023.09.1016

Abstract

Cardiometabolic disease (CMD) refers to the single or simultaneous occurrence of pathological changes in the metabolic and cardiovascular systems that can mutually influence each other, which is a collective term for metabolic and cardiovascular diseases,including obesity,insulin resistance,metabolic syndrome,diabetes,and coronary heart disease, etc. Adipokines play a critical role in the occurrence and development of CMD. Complement C1q TNF-related protein 7 (CTRP7) is a recently discovered adipokine closely associated with CMD, such as obesity, diabetes and coronary heart disease. Focusing on the biological characteristics of CTRP7, this article reviews its role in the occurrence and development of CMD, including obesity, type 2 diabetes mellitus and coronary heart disease, as well as the possible mechanisms such as regulating glucose and lipid metabolism, decreasing insulin sensitivity, promoting inflammatory responses and increasing oxidative stress, so as to provide evidence and references for CTRP7 as a therapeutic target of CMD.
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