Guidotti A, Baraldi M, Schwartz J P, Costa E
Pharmacol Biochem Behav. 1979 May;10(5):803-7. doi: 10.1016/0091-3057(79)90338-1.
Using radioreceptor assay techniques to measure the kinetics of GABA and diazepam receptors, a relationship between GABA and benzodiazepine receptors has been firmly established in membranes of brain and neuroblastoma NB2a clonal cell lines. Occupancy of benzodiazepine receptors uncovers a new population of GABA receptors (GABA2 receptors) endowed with high affinity for GABA. Moreover, stimulation of GABA receptors increases the affinity of 1,4-benzodiazepine receptors for 1,4-benzodiazepines. This reciprocal interaction appears to be mediated by an endogenous regulatory protein (for details on this protein see [14 and 29]) which allosterically regulates GABA2 receptors while it competitively interacts with benzodiazepines for their specific binding sites. The rank order of potency of the various 1,4-benzodiazepines to block the action of this protein inhibitor on GABA receptors is related to their capacity to displace 3H-diazepam binding. These data suggest that the interaction between the 1,4-benzodiazepine receptors and the endogenous protein modulator of GABA2 receptors might play a role in the pharmacological action of the 1,4-benzodiazepines.
运用放射受体分析技术来测定γ-氨基丁酸(GABA)和地西泮受体的动力学,已在脑和神经母细胞瘤NB2a克隆细胞系的膜中牢固确立了GABA与苯二氮䓬受体之间的关系。苯二氮䓬受体的占据揭示了一群对GABA具有高亲和力的新的GABA受体(GABA2受体)。此外,刺激GABA受体会增加1,4-苯二氮䓬受体对1,4-苯二氮䓬类药物的亲和力。这种相互作用似乎是由一种内源性调节蛋白介导的(关于该蛋白的详细信息见[14和29]),该蛋白对GABA2受体进行变构调节,同时它与苯二氮䓬类药物竞争其特异性结合位点。各种1,4-苯二氮䓬类药物阻断这种蛋白抑制剂对GABA受体作用的效价顺序与其取代3H-地西泮结合的能力相关。这些数据表明,1,4-苯二氮䓬受体与GABA2受体的内源性蛋白调节剂之间的相互作用可能在1,4-苯二氮䓬类药物的药理作用中发挥作用。