SPECIES-DIFFERENCES IN THE PHARMACOLOGY OF TERMINAL 5-HT AUTORECEPTORS IN MAMMALIAN BRAIN

被引：330

作者：

HOYER, D ^{[1
]}

MIDDLEMISS, DN ^{[1
]}

机构：

[1] MERCK SHARP & DOHME,NEUROSCI RES CTR,HARLOW CM2 0QR,ESSEX,ENGLAND

来源：

TRENDS IN PHARMACOLOGICAL SCIENCES | 1989年 / 10卷 / 04期

关键词：

D O I：

10.1016/0165-6147(89)90159-4

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：130 / 132

页数：3

共 29 条

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[14] IDENTIFICATION OF A 5-HT1 RECOGNITION SITE IN HUMAN-BRAIN MEMBRANES DIFFERENT FROM 5-HT1A,5-HT1B AND 5-HT1C SITES [J].

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[15]

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[16]

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[18]

MIDDLEMISS DN, 1984, N-S ARCH PHARMACOL, V327, P18, DOI 10.1007/BF00504986

[19] THE PUTATIVE 5-HT1 RECEPTOR AGONIST, RU-24969, INHIBITS THE EFFLUX OF 5-HYDROXYTRYPTAMINE FROM RAT FRONTAL-CORTEX SLICES BY STIMULATION OF THE 5-HT AUTORECEPTOR [J].

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[20] A PHARMACOLOGICAL ANALYSIS OF THE 5-HT RECEPTOR MEDIATING INHIBITION OF 5-HT RELEASE IN THE GUINEA-PIG FRONTAL-CORTEX [J].

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