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血清素(7)受体(5-HT(7)Rs)及其配体。

Serotonin(7) receptors (5-HT(7)Rs) and their ligands.

作者信息

Leopoldo M

机构信息

Universita degli Studi di Bari, Dipartimento Farmaco-Chimico, via Orabona 4, 70125 Bari, Italy.

出版信息

Curr Med Chem. 2004 Mar;11(5):629-61. doi: 10.2174/0929867043455828.

DOI:10.2174/0929867043455828
PMID:15032609
Abstract

Serotonin (5-HT) is involved in various physiological and pathological processes by interaction with 14 distinct receptor subtypes, grouped in seven classes of receptors (5-HT(1-7)) on the basis of amino acid sequence, pharmacology, and signal transduction pathways. The 5-HT(7)R is a G-protein coupled receptor with seven transmembrane domains. It was found by the application of molecular cloning and has been identified in rat, mouse, human, pig, and guinea pig. Although the biological functions of the 5-HT(7)Rs are poorly understood, preliminary evidence suggests that it may be involved in depression, control of circadian rhythms, and relaxation of vascular smooth muscles. For these reasons, the 5-HT(7)R has become a target for the development of novel drugs. This review will give a brief introduction of the pharmacology of 5-HT(7)R (molecular structure, distribution of 5-HT(7)R mRNA, localization of the 5-HT(7)R protein, functional correlates, and therapeutic potential) and a detailed survey of the 5-HT(7)R ligands, which have appeared in the literature in both papers and patents. Structure-activity relationships (SAR) of these ligands will also be described.

摘要

血清素(5-羟色胺,5-HT)通过与14种不同的受体亚型相互作用参与多种生理和病理过程,这些受体亚型根据氨基酸序列、药理学及信号转导途径被分为七类受体(5-HT(1 - 7))。5-HT(7)R是一种具有七个跨膜结构域的G蛋白偶联受体。它是通过分子克隆技术发现的,已在大鼠、小鼠、人类、猪和豚鼠中得到鉴定。尽管对5-HT(7)R的生物学功能了解甚少,但初步证据表明它可能参与抑郁症、昼夜节律调控以及血管平滑肌舒张。基于这些原因,5-HT(7)R已成为新型药物研发的靶点。本综述将简要介绍5-HT(7)R的药理学(分子结构、5-HT(7)R mRNA的分布、5-HT(7)R蛋白的定位、功能关联及治疗潜力),并详细综述文献(包括论文和专利)中出现的5-HT(7)R配体。还将描述这些配体的构效关系(SAR)。

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