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体外阿片受体测定

In vitro opioid receptor assays.

作者信息

Taylor David A

机构信息

The Department of Pharmacology and Toxicology, The Brody School of Medicine at East Carolina University, Greenville, North Carolina, USA.

出版信息

Curr Protoc Pharmacol. 2011 Dec;Chapter 4:Unit 4.8.1-34. doi: 10.1002/0471141755.ph0408s55.

Abstract

Although opioid analgesics have been used for centuries, identification of opioid receptors and the ability of an opioid receptor antagonist to block natural pain processes prompted a search for endogenous opioid peptides. In vitro models were needed to characterize opioid activity in biological samples. The longitudinal muscle/myenteric plexus (LM/MP) of the guinea pig ileum was the classical in vitro assay system, but the development of the mouse vas deferens (MVD) assay provided another important model that could be employed. Both assays entail electrical stimulation of intramural nerves to produce muscle contractions of the target organ. The robust contractions of the LM/MP are inhibited by µ and κ opioid receptor agonists, while the more labile contractions of the MVD are inhibited by µ, κ, and δ opioid receptor agonists. These in vitro assay systems are useful for evaluating biological activity of unknown substances and studying the properties of drug tolerance and both are described in this unit.

摘要

尽管阿片类镇痛药已使用了数百年,但阿片受体的鉴定以及阿片受体拮抗剂阻断自然疼痛过程的能力促使人们寻找内源性阿片肽。需要体外模型来表征生物样品中的阿片活性。豚鼠回肠的纵行肌/肌间神经丛(LM/MP)是经典的体外检测系统,但小鼠输精管(MVD)检测的发展提供了另一个可采用的重要模型。两种检测都需要对壁内神经进行电刺激以产生靶器官的肌肉收缩。LM/MP的强烈收缩受到μ和κ阿片受体激动剂的抑制,而MVD较不稳定的收缩受到μ、κ和δ阿片受体激动剂的抑制。这些体外检测系统可用于评估未知物质的生物活性以及研究药物耐受性的特性,本单元将对两者进行描述。

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