STEREOSELECTIVE BLOCKADE AT [H-3]5-HT BINDING-SITES AND AT THE 5-HT AUTORECEPTOR BY PROPRANOLOL

被引：211

作者：

MIDDLEMISS, DN

机构：

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY | 1984年 / 101卷 / 3-4期

关键词：

D O I：

10.1016/0014-2999(84)90173-0

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：289 / 293

页数：5

共 10 条

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[5] COMPARISON OF THE PHARMACOLOGICAL CHARACTERISTICS OF 5-HT1 AND 5-HT2 BINDING-SITES WITH THOSE OF SEROTONIN AUTORECEPTORS WHICH MODULATE SEROTONIN RELEASE [J].

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[6] DIRECT EVIDENCE FOR AN INTERACTION OF BETA-ADRENERGIC BLOCKERS WITH 5-HT RECEPTOR [J].

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[7] 8-HYDROXY-2-(DI-NORMAL-PROPYLAMINO)-TETRALIN DISCRIMINATES BETWEEN SUBTYPES OF THE 5-HT1 RECOGNITION SITE [J].

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FOZARD, JR .

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[8]

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NAHORSKI SR, 1983, BRIT J PHARMACOL, V78, P1071

[10] DISCRIMINATION OF MULTIPLE [H-3]5-HYDROXYTRYPTAMINE BINDING-SITES BY THE NEUROLEPTIC SPIPERONE IN RAT-BRAIN [J].

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