THE 5-HT1A RECEPTOR ANTAGONIST (S)-UH-301 BLOCKS THE (R)-8-OH-DPAT-INDUCED INHIBITION OF SEROTONERGIC DORSAL RAPHE CELL FIRING IN THE RAT

被引:29
作者
ARBORELIUS, L
HOOK, BB
HACKSELL, U
SVENSSON, TH
机构
[1] KAROLINSKA INST, DEPT PHYSIOL & PHARMACOL, DIV PHARMACOL, S-17177 STOCKHOLM, SWEDEN
[2] UPPSALA UNIV, DEPT ORGAN PHARMACEUT CHEM, UPPSALA, SWEDEN
关键词
5-HT1A; 8-OH-DPAT; (S)-UH-301; 5-HT1A RECEPTOR ANTAGONIST; ELECTROPHYSIOLOGY; DORSAL RAPHE NUCLEUS;
D O I
10.1007/BF01294785
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
(S)-UH-301 [(S)-5-fluoro-8-hydroxy-2-(dipropylamino) 0.5-4.0 mg/kg i.v.] did not significantly alter the firing rate of 5-hydroxytryptamine (5-HT) containing neurons in the dorsal raphe nucleus (DRN) as a group, although some individual cells were activated whereas others were depressed. However, (S)-UH-301 (2.0 mg/kg i.v.) consistently reversed the inhibition of DRN-5-HT cells produced by the selective 5-HT1A receptor agonist (R)-8-OH-DPAT (0.5 mu g/kg i.v.) and the dose-response curve for this effect of (R)-8-OH-DPAT was markedly shifted to the right by pretreatment with (S)-UH-301 (1.0 mg/kg i.v.). These results support the notion that (S)-UH-301 acts as an antagonist at central 5-HT1A receptors.
引用
收藏
页码:179 / 186
页数:8
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