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血管紧张素受体的激动剂-拮抗剂相互作用:双态受体模型的应用

Agonist-antagonist interactions at angiotensin receptors: application of a two-state receptor model.

作者信息

Robertson M J, Dougall I G, Harper D, McKechnie K C, Leff P

机构信息

Department of Pharmacology, Fisons, Loughborough, Leicestershire, UK.

出版信息

Trends Pharmacol Sci. 1994 Oct;15(10):364-9. doi: 10.1016/0165-6147(94)90156-2.

Abstract

Interactions between agonists and antagonists at angiotensin receptors are characterized by a number of features: variation of antagonist dynamics between apparent simple competition, insurmountable antagonism and, occasionally, augmentation; the tendency for insurmountable antagonism to be saturable; slow recovery of agonist responses following agonist-induced tachyphylaxis; and the ability of competitive antagonists to accelerate recovery from the latter intervention. Some of these phenomena have also been observed in studies of 5-HT2 receptors where they were attributed to the operation of a two-state model with an allosteric site. In this article, Mark Robertson and colleagues propose that the properties of angiotensin AT1 receptors may be explained by a similar model, but without the need to evoke an allosteric site.

摘要

血管紧张素受体上激动剂与拮抗剂之间的相互作用具有多个特点

拮抗剂动力学在明显的简单竞争、不可逾越的拮抗作用以及偶尔的增强作用之间存在变化;不可逾越的拮抗作用具有饱和倾向;激动剂诱导快速耐受后激动剂反应的缓慢恢复;以及竞争性拮抗剂加速从后一种干预中恢复的能力。在5-HT2受体的研究中也观察到了其中一些现象,这些现象被归因于具有变构位点的双态模型的作用。在本文中,马克·罗伯逊及其同事提出,血管紧张素AT1受体的特性可能由类似的模型来解释,但无需引入变构位点。

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