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Chronic exposure to Ro 15-1788: differential effect on flunitrazepam binding to cortex and hippocampus.

作者信息

Urbancic M, Marczynski T J

机构信息

Department of Pharmacology, University of Illinois College of Medicine, Chicago 60612.

出版信息

Eur J Pharmacol. 1989 Nov 14;171(1):1-7. doi: 10.1016/0014-2999(89)90423-8.

DOI:10.1016/0014-2999(89)90423-8
PMID:2515067
Abstract

The time course of changes in specific [3H]flunitrazepam binding following 2 weeks of treatment with the benzodiazepine antagonist Ro 15-1788 (2.7 and 4 mg/kg per day in drinking water) was studied in the rat neocortical and hippocampal synaptosomal membranes. Such a treatment produced regional increases in the density of benzodiazepine sites, which remained for up to 24 and 48 h after drug withdrawal in the hippocampus and cortex, respectively; the dissociation constant (Kd) was unchanged. In addition, a significant reduction in GABA enhanced [3H]flunitrazepam binding to cortical, but not to hippocampal, membranes from Ro 15-1788-treated animals was found 72 h after drug withdrawal. These data show that there is a regional difference in responses of the GABA/benzodiazepine receptor complex following chronic in vivo exposure to Ro 15-1788 and that, beside the increases in the maximal binding (Bmax) of [3H]flunitrazepam the coupling between the GABA and the benzodiazepine recognition sites was also affected.

摘要

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