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Inhibition of [3H]Diazepam and [3H]3-Carboethoxy-β-Carboline Binding by Irazepine: Evidence for Multiple "Domains" of the Benzodiazepine Receptor
Authors:Phil Skolnick  Margaret Schweri  Eberhard Kutter  Evan Williams  Steven Paul
Affiliation:Laboratory of Bioorgarzic Chemistry, NIADDK, National Institutes of Health, Bethesda, Maryland, U.S.A.;Neuroscience Branch, NIMH, National Institutes of Health, Bethesda, Maryland, U.S.A.
Abstract:The binding of [3H]diazepam and [3H]3-carboethoxy-beta-carboline was examined in rat brain synaptosomal membranes treated with irazepine, an alkylating benzodiazepine. Under incubation conditions that resulted in a 25-33% reduction in the Bmax of [3H]diazepam binding, only modest (less than 8.5%) reductions in the Bmax of [3H]3-carboethoxy-beta-carboline were observed. The differential effects of irazepine on the binding of these two compounds may be explained by the presence of multiple areas or "domains" on the benzodiazepine receptor.
Keywords:Diazepam    3-Carboethoxy    β-carboline    Irazepine    Domain    Benzodiazepine receptor
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