Skerritt J H, Macdonald R L
Brain Res. 1984 Apr 9;297(1):181-6. doi: 10.1016/0006-8993(84)90557-2.
GABA (4-aminobutyric acid) and its bicyclic analog THIP (4,5,6,7-tetrahydroisoxazolo-[4,5-c]-pyridin-3-ol) produced membrane hyperpolarization and increased chloride ion conductance of mouse spinal cord neurons in cell culture. Above 1 nM diazepam enhanced the actions of both GABA and THIP with similar potency and efficacy. Diazepam has been shown to enhance the binding of [3H]GABA to rat brain membranes over similar concentration ranges, with the EC50 values for enhancement of [3H]GABA binding and increase in membrane conductance being similar. In contrast, binding of [3H]THIP has been shown to be unaltered by diazepam under a variety of conditions. The possible reasons for such a discrepancy between these electrophysiological and neurochemical results with THIP are discussed.
γ-氨基丁酸(GABA,4-氨基丁酸)及其双环类似物THIP(4,5,6,7-四氢异恶唑并-[4,5-c]-吡啶-3-醇)可使细胞培养的小鼠脊髓神经元发生膜超极化,并增加氯离子电导。在浓度高于1 nM时,地西泮以相似的效力和效能增强GABA和THIP的作用。已表明,在相似的浓度范围内,地西泮可增强[3H]GABA与大鼠脑膜的结合,增强[3H]GABA结合的EC50值与膜电导增加的EC50值相似。相比之下,在各种条件下,地西泮均未改变[3H]THIP的结合。本文讨论了这些关于THIP的电生理和神经化学结果之间存在差异的可能原因。