Sieghart W
Abteilung für Biochemische Psychiatrie, der Psychiatrischen Universitätsklinik, Wien.
Wien Klin Wochenschr. 1990 Mar 30;102(7):197-201.
GABAA-benzodiazepine receptors and epilepsy. gamma-Aminobutyric acid (GABA) is quantitatively one of the most important neurotransmitters in the central nervous system. Since the predominant action of GABA on neurons is inhibitory, activation of GABA receptors, and especially of GABAA receptors, causes an anticonvulsive effect. GABAA receptors can be activated either directly by GABA or GABA-agonists, or indirectly by allosteric modulation of these receptors. For instance, benzodiazepines enhance the postsynaptic actions of GABA by binding to benzodiazepine receptors which are allosteric modulatory binding sites on GABAA receptors. Conversely, there are compounds which bind to the same benzodiazepine receptors, but reduce the postsynaptic actions of GABA. These compounds cause convulsions and are called "inverse agonists" of the benzodiazepine receptors. Recent evidence indicates the existence of several different benzodiazepine receptor (and, thus, GABAA receptor) subtypes. Since these receptor subtypes exhibit a different regional distribution in the central nervous system, the development of subtype-selective GABAA receptor agonists or benzodiazepine receptor agonists should result in anticonvulsants with less side effects.
GABAA-苯二氮䓬受体与癫痫。γ-氨基丁酸(GABA)在数量上是中枢神经系统中最重要的神经递质之一。由于GABA对神经元的主要作用是抑制性的,GABA受体尤其是GABAA受体的激活会产生抗惊厥作用。GABAA受体可直接被GABA或GABA激动剂激活,也可通过这些受体的变构调节间接激活。例如,苯二氮䓬类药物通过与苯二氮䓬受体结合来增强GABA的突触后作用,苯二氮䓬受体是GABAA受体上的变构调节结合位点。相反,有些化合物与相同的苯二氮䓬受体结合,但会降低GABA的突触后作用。这些化合物会引发惊厥,被称为苯二氮䓬受体的“反向激动剂”。最近的证据表明存在几种不同的苯二氮䓬受体(因此也存在GABAA受体)亚型。由于这些受体亚型在中枢神经系统中表现出不同的区域分布,开发亚型选择性GABAA受体激动剂或苯二氮䓬受体激动剂应能产生副作用较小的抗惊厥药物。