Uusi-Oukari M
Tampere Brain Research Center, Department of Biomedical Sciences, University of Tampere, Finland.
J Neurochem. 1992 Aug;59(2):560-7. doi: 10.1111/j.1471-4159.1992.tb09406.x.
The effects of treatment of brain membranes with diethyl pyrocarbonate (DEP), a histidine-modifying reagent, on the binding of 3H-labeled Ro 15-4513 (ethyl-8-azido-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a]- [1,4]benzodiazepine-3-carboxylate) and [3H]diazepam were compared. DEP pretreatment produced a dose-dependent decrease in [3H]diazepam binding, whereas low DEP concentrations enhanced the binding of [3H]Ro 15-4513. These effects were reversed by incubation with hydroxylamine after the treatment. The enhancement of [3H]Ro 15-4513 binding was due to an increase in the affinity of the binding sites (KD), without any effect on binding capacity (Bmax). The enhancement was perceived in cerebral cortical, cerebellar, and hippocampal membranes. DEP treatment decreased the displacement of [3H]Ro 15-4513 binding by diazepam and FG 7142 (N-methyl-beta-carboline-3-carboxamide) but not by Ro 15-4513 and Ro 19-4603 (tert-butyl-5,6-dihydro-5-methyl-6-oxo-4H-imidazol[1,5- a]thieno[2,3-f][1,4]diazepine-3-carboxylate). Although the stimulating effect of gamma-aminobutyric acid (GABA) on [3H]-diazepam binding was not affected by DEP treatment, such treatment reduced the inhibitory effect of GABA on [3H]Ro 15-4513 binding. The enhancement of [3H]Ro 15-4513 binding was observed in membranes pretreated with DEP in the presence of flunitrazepam, whereas such pretreatment reduced significantly the inhibitory effect of DEP on [3H]-diazepam binding.(ABSTRACT TRUNCATED AT 250 WORDS)
比较了用焦碳酸二乙酯(DEP,一种组氨酸修饰试剂)处理脑膜对3H标记的Ro 15 - 4513(8 - 叠氮基 - 5,6 - 二氢 - 5 - 甲基 - 6 - 氧代 - 4H - 咪唑并[1,5 - a][1,4]苯并二氮杂䓬 - 3 - 羧酸乙酯)和[3H]地西泮结合的影响。DEP预处理使[3H]地西泮结合呈剂量依赖性降低,而低浓度的DEP增强了[3H]Ro 15 - 4513的结合。处理后用羟胺孵育可逆转这些效应。[3H]Ro 15 - 4513结合的增强是由于结合位点亲和力(KD)增加,而对结合容量(Bmax)无影响。在大脑皮质、小脑和海马体膜中观察到这种增强。DEP处理降低了地西泮和FG 7142(N - 甲基 - β - 咔啉 - 3 - 甲酰胺)对[3H]Ro 15 - 4513结合的置换作用,但Ro 15 - 4513和Ro 19 - 4603(叔丁基 - 5,6 - 二氢 - 5 - 甲基 - 6 - 氧代 - 4H - 咪唑并[1,5 - a]噻吩并[2,3 - f][1,4]二氮杂䓬 - 3 - 羧酸酯)没有这种作用。虽然γ - 氨基丁酸(GABA)对[3H] - 地西泮结合的刺激作用不受DEP处理的影响,但这种处理降低了GABA对[3H]Ro 15 - 4513结合的抑制作用。在氟硝西泮存在下用DEP预处理的膜中观察到[3H]Ro 15 - 4513结合增强,而这种预处理显著降低了DEP对[3H] - 地西泮结合的抑制作用。(摘要截断于250字)