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多种阿片受体:似曾相识的感觉再次袭来。

Multiple opiate receptors: déjà vu all over again.

作者信息

Pasternak Gavril W

机构信息

Department of Neurology, Laboratory of Molecular Pharmacology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.

出版信息

Neuropharmacology. 2004;47 Suppl 1:312-23. doi: 10.1016/j.neuropharm.2004.07.004.

Abstract

The concept of multiple opioid receptors has changed dramatically since their initial proposal by Martin nearly 40 years ago. Three major opioid receptor families have now been proposed: mu, kappa and delta. Most of the opioid analgesics used clinically selectively bind to mu opioid receptors. Yet, clinicians have long appreciated subtle, but significant, differences in their pharmacology. These observations suggested more than one mu opioid receptor mechanism of action and led us to propose multiple mu opioid receptors over 20 years ago based upon a range of pharmacological and receptor binding approaches. A mu opioid receptor, MOR-1, was cloned about a decade ago. More recent studies have now identified a number of splice variants of this clone. These splice variants may help explain the pharmacology of the mu opioids and open interesting directions for future opioid research.

摘要

自近40年前马丁首次提出多种阿片受体的概念以来,这一概念已经发生了巨大变化。现在已经提出了三大阿片受体家族:μ、κ和δ。临床上使用的大多数阿片类镇痛药选择性地与μ阿片受体结合。然而,临床医生早就认识到它们在药理学上存在细微但显著的差异。这些观察结果表明存在不止一种μ阿片受体作用机制,基于一系列药理学和受体结合方法,我们在20多年前就提出了多种μ阿片受体。大约十年前克隆出了一种μ阿片受体MOR-1。最近的研究现已鉴定出该克隆的许多剪接变体。这些剪接变体可能有助于解释μ阿片类药物的药理学,并为未来的阿片类药物研究开辟有趣的方向。

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