MODULATION OF BENZODIAZEPINE BINDING-SITE SENSITIVITY

被引:34
作者
TALLMAN, JF
GALLAGER, DW
机构
[1] Section on Biochemistry and Pharmacology, Biological Psychiatry Branch National Institute of Mental Health Bethesda
关键词
Benzodiazepine; Diazepam; Diphenylhydantoin; GABA; Muscimol;
D O I
10.1016/0091-3057(79)90339-3
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Recent studies on agents which alter benzodiazepane binding site sensitivity in brain are described. GABAergic agonists enhance and antagonists inhibit binding to the brain specific benzodiazepine binding site, and the binding can be correlated with effects on neuronal cell firing in the dorsal raphe nucleus. Anions such as chloride, iodide and nitrite also enhance (3H)diazepam binding and this enhancement is consistent with their role in postsynaptic inhibition. Pretreatment of animals with the anticonvulsant, diphenylhydantoin, enhances both diazepam binding and the electrophysiological response to diazepam suggesting one possible locus for the anticonvulsant action of diphenylhydantoin in brain. Take together, these results suggest the existence of a GABA/Cl- ionophore/BZ binding complex in brain. Preliminary results on the purification of the BZ component of this complex and flourescent probes for its study are described. © 1979.
引用
收藏
页码:809 / 813
页数:5
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