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嘌呤离子型(P2X)受体。

Purine ionotropic (P2X) receptors.

作者信息

Köles L, Fürst S, Illes P

机构信息

Rudolf-Boehm-Institute of Pharmacology and Toxicology, University of Leipzig, Germany.

出版信息

Curr Pharm Des. 2007;13(23):2368-84. doi: 10.2174/138161207781368747.

Abstract

Purinergic signaling is involved in the proper functioning of virtually all organs of the body. Although in some cases purines have a major influence on physiological functions (e.g. thrombocyte aggregation), more often they are just background modulators contributing to fine tuning of biological events. However, under pathological conditions, when a huge amount of adenosine 5'-triphosphate (ATP) can reach the extracellular space, their significance is increasing. ATP and its various degradation products activate membrane receptors divided into two main classes: the metabotropic P2Y and the ionotropic P2X family. This latter group, the purine ionotropic receptor, is the object of this review. After providing a description about the distribution and functional properties of P2X receptors in the body, their pharmacology will be summarized. In the second part of this review, the role of purines in those organ systems and body functions will be highlighted, where the (patho)physiological role of P2X receptors has been suggested or is even well established. Besides the regulation of organ systems, for instance in the cardiovascular, respiratory, genitourinary or gastrointestinal system, some special issues will also be discussed, such as the role of P2X receptors in pain, tumors, central nervous system (CNS) injury and embryonic development. Several examples will indicate that purine ionotropic receptors might serve as attractive targets for pharmacological interventions in various diseases, and that selective ligands for these receptors will probably constitute important future therapeutic tools in humans.

摘要

嘌呤能信号传导参与身体几乎所有器官的正常运作。虽然在某些情况下嘌呤对生理功能有重大影响(如血小板聚集),但它们更多时候只是有助于生物事件微调的背景调节剂。然而,在病理条件下,当大量的5'-三磷酸腺苷(ATP)能够到达细胞外空间时,它们的重要性就会增加。ATP及其各种降解产物激活分为两大类的膜受体:代谢型P2Y和离子型P2X家族。后一组,即嘌呤离子型受体,是本综述的对象。在描述了P2X受体在体内的分布和功能特性后,将总结它们的药理学。在本综述的第二部分,将重点介绍嘌呤在那些器官系统和身体功能中的作用,其中P2X受体的(病理)生理作用已被提出或甚至已得到充分证实。除了对器官系统的调节,例如在心血管、呼吸、泌尿生殖或胃肠道系统中,还将讨论一些特殊问题,如P2X受体在疼痛、肿瘤、中枢神经系统(CNS)损伤和胚胎发育中的作用。几个例子将表明,嘌呤离子型受体可能是各种疾病药物干预的有吸引力的靶点,并且这些受体的选择性配体可能构成未来人类重要的治疗工具。

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