速激素受体和受体亚型。

R Patacchini, C A Maggi
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引用次数: 0

摘要

速激肽,即P物质、神经激肽A和神经激肽B,是广泛分布于哺乳动物中枢和周围神经系统的一类神经肽。在周围神经系统中,感觉神经末梢释放的速激肽是神经源性炎症现象的原因。在脊髓/中枢神经系统中,速激素在疼痛传递/感知和一些自主反射和行为中发挥作用。它们的作用由三种不同的受体介导,称为NK1, NK2和NK3。所有速激素受体都属于G蛋白偶联受体超家族,具有7个假定的跨膜跨越片段。在过去的几年中,针对NK1, NK2和NK3受体,已经开发了许多有效的和选择性的多肽和非多肽拮抗剂。目前,三种速激肽受体的分离和克隆使我们能够研究天然速激肽与其受体相互作用的分子决定因素,以及拮抗剂干预这一过程的机制。此外,速激肽拮抗剂的引入揭示了速激肽受体之间惊人的物种相关异质性,并提示NK1和NK2受体可能存在物种内异质性。然而,需要分子生物学研究来证明真正的速激肽受体亚型的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tachykinin receptors and receptor subtypes.

The tachykinins, substance P, neurokinin A and neurokinin B, are a family of neuropeptides widely distributed in the mammalian central and peripheral nervous system. In the peripheral nervous system, tachykinins released from peripheral endings of sensory nerves are responsible for the neurogenic inflammation phenomenon. In the spinal cord/central nervous system, tachykinins play a role in pain transmission/perception and in some autonomic reflexes and behaviors. Their actions are mediated by three distinct receptors, termed NK1, NK2 and NK3. All tachykinin receptors belong to the superfamily of G protein-coupled receptors, with seven putative transmembrane spanning segments. In the past few years, a number of potent and selective antagonists, of both peptide and nonpeptide nature, has been developed for the NK1, NK2 and NK3 receptors. The contemporary isolation and cloning of the three tachykinin receptors enable now to study the molecular determinants for the interaction of natural tachykinins with their receptors, and the mechanism by which the antagonists interfere in this process. Furthermore, the introduction of tachykinin antagonists has revealed a striking species-related heterogeneity among the tachykinin receptors, and has also suggested a possible intra-species heterogeneity for both NK1 and NK2 receptors. However, molecular biology studies are needed to prove the existence of true tachykinin receptor subtypes.

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