作者: M.K. Ticku , T.P. Burch , W.C. Davis
DOI: 10.1016/0091-3057(83)90140-5
关键词:
摘要: Abstract Ethanol, barbiturates and benzodiazepines have similar pharmacological effects. All of these drugs facilitate the inhibitory transmission mediated by GABA administration increases number low affinity receptor sites, while, during ethanol withdrawal, this site is decreased. This decreased withdrawal correlated with audiogenic seizure activity. These results indicate that in vivo interacts receptors, interaction may be responsible for some effects symptoms withdrawal. like pentobarbital, also enhances [3H]diazepam binding to Lubrol-solubilized membrane fraction vitro. effect was dose-related blocked picrotoxinin other antagonists. Enhancement various alcohols did not correlate lipid: water partition coefficients. Ethanol partially inhibited [3H]-α-dihydropicrotoxinin fraction. ethanol, modulate benzodiazepine component benzodiazepine-GABA receptor-ionophore complex via site. The possible interpretation results, relation GABAergic transmission, discussed.