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心血管系统中的P2X受体及其作为疾病治疗靶点的潜力。

P2X receptors in the cardiovascular system and their potential as therapeutic targets in disease.

作者信息

Ralevic Vera

机构信息

School of Life Sciences, Queen's Medical Centre, Nottingham, United Kingdom, NG7 2UH.

出版信息

Curr Med Chem. 2015;22(7):851-65. doi: 10.2174/0929867321666141215094050.

Abstract

This review considers the expression and roles of P2X receptors in the cardiovascular system in health and disease and their potential as therapeutic targets. P2X receptors are ligand gated ion channels which are activated by the endogenous ligand ATP. They are formed from the assembly of three P2X subunit proteins from the complement of seven (P2X1-7), which can associate to form homomeric or heteromeric P2X receptors. The P2X1 receptor is widely expressed in the cardiovascular system, being located in the heart, in the smooth muscle of the majority of blood vessels and in platelets. P2X1 receptors expressed in blood vessels can be activated by ATP coreleased with noradrenaline as a sympathetic neurotransmitter, leading to smooth muscle depolarisation and contraction. There is evidence that the purinergic component of sympathetic neurotransmission is increased in hypertension, identifying P2X1 receptors as a possible therapeutic target in this disorder. P2X3 and P2X2/3 receptors are expressed on cardiac sympathetic neurones and may, through positive feedback of neuronal ATP at this prejunctional site, amplify sympathetic neurotransmission. Activation of P2X receptors expressed in the heart increases cardiac myocyte contractility, and an important role of the P2X4 receptor in this has been identified. Deletion of P2X4 receptors in the heart depresses contractile performance in models of heart failure, while overexpression of P2X4 receptors has been shown to be cardioprotective, thus P2X4 receptors may be therapeutic targets in the treatment of heart disease. P2X receptors have been identified on endothelial cells. Although immunoreactivity for all P2X1-7 receptor proteins has been shown on the endothelium, relatively little is known about their function, with the exception of the endothelial P2X4 receptor, which has been shown to mediate endothelium-dependent vasodilatation to ATP released during shear stress. The potential of P2X receptors as therapeutic targets in the treatment of cardiovascular disease is discussed.

摘要

本综述探讨了P2X受体在健康和疾病状态下心血管系统中的表达、作用及其作为治疗靶点的潜力。P2X受体是配体门控离子通道,可被内源性配体ATP激活。它们由七种P2X亚基蛋白(P2X1 - 7)中的三种组装而成,可形成同源或异源P2X受体。P2X1受体在心血管系统中广泛表达,存在于心脏、大多数血管的平滑肌和血小板中。血管中表达的P2X1受体可被与去甲肾上腺素共同释放的ATP激活,去甲肾上腺素作为一种交感神经递质,导致平滑肌去极化和收缩。有证据表明,高血压患者交感神经传递中的嘌呤能成分增加,这表明P2X1受体可能是该疾病的一个治疗靶点。P2X3和P2X2/3受体表达于心脏交感神经元上,可能通过神经末梢部位神经元ATP的正反馈作用来增强交感神经传递。心脏中表达的P2X受体激活可增加心肌细胞收缩力,并且已确定P2X4受体在此过程中起重要作用。在心力衰竭模型中,心脏中P2X4受体的缺失会降低收缩功能,而P2X4受体的过表达已被证明具有心脏保护作用,因此P2X4受体可能是治疗心脏病的治疗靶点。在内皮细胞上也已鉴定出P2X受体。虽然在内皮上已显示出所有P2X1 - 7受体蛋白的免疫反应性,但除了内皮P2X4受体外,对它们的功能了解相对较少。内皮P2X4受体已被证明可介导对剪切应力期间释放的ATP的内皮依赖性血管舒张。本文还讨论了P2X受体作为心血管疾病治疗靶点的潜力。

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