Pathophysiological relevance and therapeutic outlook of GPR43 in atherosclerosis

G蛋白偶联受体 炎症 受体 病理生理学 脂蛋白 氧化应激 血脂异常 载脂蛋白B 生物 内皮功能障碍 发病机制 药理学 生物信息学 生物化学 内分泌学 胆固醇 糖尿病 免疫学
作者
Mu-Yao Tang,Hao Xie,Jin-Tao Tao,Chun Zhang,Yao-Hua Luo,Cong Zhang,Si-Qin Peng,Lin-Xi Xie,Wen-Bo Lv,Chi Zhang,Liang Huang
出处
期刊:Biochemistry and Cell Biology [NRC Research Press]
卷期号:102 (6): 418-429 被引量:1
标识
DOI:10.1139/bcb-2024-0053
摘要

Atherosclerosis (AS) is an inflammatory arterial disorder that occurs due to the deposition of the excessive lipoprotein under the artery intima, mainly including low-density lipoprotein and other apolipoprotein B-containing lipoproteins. G protein-coupled receptors (GPCRs) play a crucial role in transmitting signals in physiological and pathophysiological conditions. GPCRs recognize inflammatory mediators, thereby serving as important players during chronic inflammatory processes. It has been demonstrated that free fatty acids can function as ligands for various GPCRs, such as free fatty acid receptor (FFAR)1/GPR40, FFAR2/GPR43, FFAR3/GPR41, FFAR4/GPR120, and the lipid metabolite binding glucose-dependent insulinotropic receptor (GPR119). This review discusses GPR43 and its ligands in the pathogenesis of AS, especially focusing on its distinct role in regulating chronic vascular inflammation, inhibiting oxidative stress, ameliorating endothelial dysfunction and improving dyslipidemia. It is hoped that this review may provide guidance for further studies aimed at GPR43 as a promising target for drug development in the prevention and therapy of AS.
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