Emerging roles for orphan G-protein-coupled receptors in the cardiovascular system

Sidath Katugampola , Anthony Davenport
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Abstract

Despite current drug therapies, including those that target enzymes, channels and known G-protein-coupled receptors (GPCRs), cardiovascular disease remains the major cause of ill health, which suggests that other transmitter systems might be involved in this disease. In humans, ∼175 genes have been predicted to encode ‘orphan’ GPCRs, where the endogenous ligand is not yet known. As a result of intensive screening using ‘reverse pharmacology’, an increasing number of orphan receptors are being paired with their cognate ligands, many of which are peptides. The existence of some of these peptides such as urotensin-II and relaxin had been known for some time but others, including ghrelin and apelin, represent novel sequences. The pharmacological characterization of these emerging peptide–receptor systems is a tantalising area of cardiovascular research, with the prospect of identifying new therapeutic targets.

孤儿g蛋白偶联受体在心血管系统中的新作用
尽管目前的药物治疗,包括那些针对酶、通道和已知的g蛋白偶联受体(gpcr)的药物治疗,心血管疾病仍然是健康不良的主要原因,这表明其他递质系统可能与这种疾病有关。在人类中,预计约有175个基因编码“孤儿”gpcr,其中内源性配体尚不清楚。由于使用“反向药理学”进行密集筛选,越来越多的孤儿受体正在与其同源配体配对,其中许多是肽。其中一些肽的存在,如尿紧张素- ii和松弛素,已经为人所知一段时间了,但其他的,包括胃饥饿素和apelin,代表了新的序列。这些新兴肽受体系统的药理学特征是心血管研究的一个诱人领域,具有确定新的治疗靶点的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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