首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Molecular, pharmacological and functional diversity of 5-HT receptors.
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Molecular, pharmacological and functional diversity of 5-HT receptors.

机译:5-HT受体的分子,药理和功能多样性。

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摘要

Serotonin (5-hydroxytryptamine, 5-HT) is probably unique among the monoamines in that its effects are subserved by as many as 13 distinct heptahelical, G-protein-coupled receptors (GPCRs) and one (presumably a family of) ligand-gated ion channel(s). These receptors are divided into seven distinct classes (5-HT(1) to 5-HT(7)) largely on the basis of their structural and operational characteristics. Whilst this degree of physical diversity clearly underscores the physiological importance of serotonin, evidence for an even greater degree of operational diversity continues to emerge. The challenge for modern 5-HT research has therefore been to define more precisely the properties of the systems that make this incredible diversity possible. Much progress in this regard has been made during the last decade with the realisation that serotonin is possibly the least conservative monoamine transmitter and the cloning of its many receptors. Coupled with the actions of an extremely avid and efficient reuptake system, this array of receptor subtypes provides almost limitless signalling capabilities to the extent that one might even question the need for other transmitter systems. However, the complexity of the system appears endless, since posttranslational modifications, such as alternate splicing and RNA editing, increase the number of proteins, oligomerisation and heteromerisation increase the number of complexes, and multiple G-protein suggest receptor trafficking, allowing phenotypic switching and crosstalk within and possibly between receptor families. Whether all these possibilities are used in vivo under physiological or pathological conditions remains to be firmly established, but in essence, such variety will keep the 5-HT community busy for quite some time. Those who may have predicted that molecular biology would largely simplify the life of pharmacologists have missed the point for 5-HT research in particular and, most probably, for many other transmitters. This chapter is an attempt to summarise very briefly 5-HT receptor diversity. The reward for unravelling this complex array of serotonin receptor--effector systems may be substantial, the ultimate prize being the development of important new drugs in a range of disease areas.
机译:5-羟色胺(5-羟色胺,5-HT)在单胺中可能是独特的,因为其作用可被多达13种不同的七螺旋G蛋白偶联受体(GPCR)和一个(可能是一个家族)配体门控离子通道。这些受体主要根据其结构和操作特征分为七个不同的类别(5-HT(1)至5-HT(7))。尽管这种程度的身体多样性显然强调了5-羟色胺的生理重要性,但仍出现了更高程度的操作多样性的证据。因此,现代5-HT研究面临的挑战是更精确地定义使这种难以置信的多样性成为可能的系统属性。在过去的十年中,随着人们认识到5-羟色胺可能是最不保守的单胺递质和其许多受体的克隆,在这方面已经取得了很大进展。加上极为活跃和高效的重摄取系统的作用,这种受体亚型阵列提供了几乎无限的信号传递能力,以至于甚至有人可能质疑对其他发射器系统的需求。但是,系统的复杂性似乎无穷无尽,因为翻译后修饰(例如交替剪接和RNA编辑)会增加蛋白质的数量,寡聚和异源化会增加复合物的数量,并且多个G蛋白提示受体转运,从而允许表型转换和受体家族内部和之间可能发生串扰。是否在生理或病理条件下在体内使用所有这些可能性尚待确定,但从本质上讲,这种多样性将使5-HT社区忙碌一段时间。那些可能已经预测到分子生物学将大大简化药理学家生命的人,尤其是在5-HT研究中,甚至在许多其他发射器中,都错过了这一点。本章试图简要总结5-HT受体的多样性。解开这种复杂的血清素受体-效应器系统阵列可能会获得丰厚的回报,最终的奖项是在一系列疾病领域开发重要的新药。

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