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二苯基烷基胺类钙拮抗剂与主动脉膜中的α-肾上腺素能受体结合位点相互作用。

Diphenylalkylamine calcium antagonists interact with alpha-adrenoceptor binding sites in aortic membranes.

作者信息

Descombes J J, Stoclet J C

出版信息

Eur J Pharmacol. 1985 Sep 24;115(2-3):313-6. doi: 10.1016/0014-2999(85)90707-1.

Abstract

Some interactions of calcium antagonists with [3H]prazosin and [3H]yohimbine binding sites were investigated in bovine aorta membranes. Diphenylalkylamines (flunarizine, cinnarizine and bepridil) acted as competitors of the two ligands with Ki values in the microM range. With the exception of verapamil, reference compounds (nifedipine, Bay-K 8644, diltiazem) and the peripheral benzodiazepine receptor antagonist PK 11195 did not displace the ligands. The apparent affinity of the diphenylalkylamines for alpha-adrenoceptor was consistent with the concentrations producing vasodilatation.

摘要

在牛主动脉膜中研究了钙拮抗剂与[3H]哌唑嗪和[3H]育亨宾结合位点的一些相互作用。二苯基烷基胺(氟桂利嗪、桂利嗪和苄普地尔)作为两种配体的竞争者,其Ki值在微摩尔范围内。除维拉帕米外,参比化合物(硝苯地平、Bay-K 8644、地尔硫䓬)和外周苯二氮䓬受体拮抗剂PK 11195不会取代这些配体。二苯基烷基胺对α-肾上腺素受体的表观亲和力与产生血管舒张的浓度一致。

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