NEURO-PHARMACOLOGICAL SPECTRUM OF MUSCIMOL

被引:56
作者
WORMS, P
DEPOORTERE, H
LLOYD, KG
机构
[1] Neuropharmacology Unit, Synthélabo-L.E.R.S., 31
关键词
D O I
10.1016/0024-3205(79)90555-1
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Muscimol was tested in comparison with a series of reference compounds in a variety of situations in which GABA-related drugs are known to have an effect. Muscimol blocked the convulsions and/or lethality due to picrotoxinin, strychnine and a low dose of bicuculline. It was inactive against higher dosis of bicuculline, metrazole or electroshock convulsions. Muscimol reduced both the basal and the picrotoxin-induced multi-unit activity of the neurons of the dorsal Deiters' nucleus ; although active at low doses, the maximum effect of muscimol was relatively weak. Muscimol potentiated neuroleptic-induced catalepsy, and this effect was bicuculline sensitive ; it did not induce catalypsy in the presence of sulpiride. At high doses muscimol blocked apomorphine-induced stereotyped behaviour. It is proposed that muscimol is a GABA agonist of high affinity but of relatively low efficacy as based on its spectrum of neuropharmacological activities in vivo". © 1979."
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收藏
页码:607 / 614
页数:8
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