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腺苷与腺苷受体:心血管系统中的“双刃剑”

Adenosine and adenosine receptors: a "double-edged sword" in cardiovascular system.

作者信息

Qian Yongqi, Zheng Yixuan, Leng Liang, Liu Qingqing, Tian Xiaojuan, Chen Shilin, Zhang Sanyin, Xie Jiang

机构信息

School of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

The Third People's Hospital of Chengdu, Clinical College of Southwest Jiao Tong University, Chengdu, China.

出版信息

Front Pharmacol. 2025 Jul 3;16:1538680. doi: 10.3389/fphar.2025.1538680. eCollection 2025.

Abstract

Adenosine serves a variety of biological purposes in the circulatory system and was first discovered in the heart in 1929. By interacting with four adenosine receptor (AR) subtypes of G protein-coupled receptors-AAR, AAR, AAR, and AAR-adenosine controls physiological processes. In pathological situations, spikes in adenosine activate the four receptor subtypes and alter downstream pathways by altering the generation of cyclic adenosine monophosphate, which contributes to autophagy and inflammation. There will inevitably be conflicting reactions from the various subtypes in this situation. Additionally, via mediating distinct signals or under various models and pathophysiological situations, the same subtype itself may have contradictory effects. Taken together, ARs' conflicting regulatory roles in the cardiovascular system not only highlight the intricacy of their physiological roles but also offer a crucial avenue for future study into the treatment of cardiovascular diseases. The contradictory regulatory roles of adenosine and ARs in cardiovascular disorders, as well as their potential as therapeutic targets, are methodically outlined in this review.

摘要

腺苷在循环系统中具有多种生物学功能,于1929年首次在心脏中被发现。通过与G蛋白偶联受体的四种腺苷受体(AR)亚型——A1AR、A2AAR、A2BAR和A3AR相互作用,腺苷可控制生理过程。在病理情况下,腺苷水平的激增会激活这四种受体亚型,并通过改变环磷酸腺苷的生成来改变下游信号通路,进而导致自噬和炎症反应。在这种情况下,不同亚型之间不可避免地会产生相互矛盾的反应。此外,同一亚型本身在介导不同信号或处于不同模型及病理生理状态下时,也可能产生相互矛盾的作用。综上所述,ARs在心血管系统中的矛盾调节作用不仅凸显了其生理功能的复杂性,也为未来心血管疾病治疗的研究提供了关键途径。本综述系统地概述了腺苷和ARs在心血管疾病中的矛盾调节作用及其作为治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7789/12267028/057155c00149/fphar-16-1538680-g001.jpg

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