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靶向腺苷受体治疗心脏纤维化

Targeting Adenosine Receptors for the Treatment of Cardiac Fibrosis.

作者信息

Vecchio Elizabeth A, White Paul J, May Lauren T

机构信息

Monash Institute of Pharmaceutical Sciences, Monash University, ParkvilleVIC, Australia.

Department of Pharmacology, Monash University, ParkvilleVIC, Australia.

出版信息

Front Pharmacol. 2017 May 5;8:243. doi: 10.3389/fphar.2017.00243. eCollection 2017.

Abstract

Adenosine is a ubiquitous molecule with key regulatory and cytoprotective mechanisms at times of metabolic imbalance in the body. Among a plethora of physiological actions, adenosine has an important role in attenuating ischaemia-reperfusion injury and modulating the ensuing fibrosis and tissue remodeling following myocardial damage. Adenosine exerts these actions through interaction with four adenosine G protein-coupled receptors expressed in the heart. The adenosine A receptor (AAR) is the most abundant adenosine receptor (AR) in cardiac fibroblasts and is largely responsible for the influence of adenosine on cardiac fibrosis. and studies demonstrate that acute AAR stimulation can decrease fibrosis through the inhibition of fibroblast proliferation and reduction in collagen synthesis. However, in contrast, there is also evidence that chronic AAR antagonism reduces tissue fibrosis. This review explores the opposing pro- and anti-fibrotic activity attributed to the activation of cardiac ARs and investigates the therapeutic potential of targeting ARs for the treatment of cardiac fibrosis.

摘要

腺苷是一种普遍存在的分子,在机体代谢失衡时具有关键的调节和细胞保护机制。在众多生理作用中,腺苷在减轻缺血再灌注损伤以及调节心肌损伤后随之而来的纤维化和组织重塑方面发挥着重要作用。腺苷通过与心脏中表达的四种腺苷G蛋白偶联受体相互作用来发挥这些作用。腺苷A受体(AAR)是心脏成纤维细胞中最丰富的腺苷受体(AR),在很大程度上负责腺苷对心脏纤维化的影响。多项研究表明,急性刺激AAR可通过抑制成纤维细胞增殖和减少胶原蛋白合成来减轻纤维化。然而,与此相反,也有证据表明,长期拮抗AAR可减少组织纤维化。本综述探讨了归因于心脏AR激活的相反的促纤维化和抗纤维化活性,并研究了靶向AR治疗心脏纤维化的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3cf/5418340/d39474cb6d75/fphar-08-00243-g001.jpg

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