Ghansah E, Weiss D S
Department of Neurobiology, University of Alabama at Birmingham, School of Medicine, 1719 Sixth Avenue South, CIRC 410, Birmingham, AL 35294-0021, USA.
Neuropharmacology. 2001 Mar;40(3):327-33. doi: 10.1016/s0028-3908(00)00166-0.
Previous studies have suggested that activation of calcium-phospholipid-dependent protein kinase (PKC) enhances benzodiazepine (BZD)- and pentobarbital (PB)- mediated potentiation of alpha(1)beta(1)gamma(2) GABA(A) receptors (GABA(A)-Rs). To delineate the underlying mechanism(s), voltage-clamp recordings were performed on recombinant alpha(1)beta(1)gamma(2) GABA(A) receptors functionally expressed in Xenopus laevis oocytes. GABA(A)-Rs were tested for their sensitivity to diazepam and PB before and after incubation in phorbol 12-myristate 13-acetate (PMA). PMA (25 nM) significantly attenuated the GABA(A) current (p<0.05, n=12-19) up to 90%. PMA treatment, however, did not alter the sensitivity to diazepam or pentobarbital. Similar results were obtained with recombinant alpha(1)beta(2)gamma(2) GABA receptors. These data suggest that PKC activation does not alter the allosteric modulation of GABA(A)-Rs by benzodiazepines and barbiturates and is consistent with the observation from other studies in oocytes that PMA decreases the amplitude of the GABA-activated currents via receptor internalization rather than modification of receptor kinetics.
先前的研究表明,钙磷脂依赖性蛋白激酶(PKC)的激活可增强苯二氮䓬(BZD)和戊巴比妥(PB)介导的α(1)β(1)γ(2)GABAA受体(GABAA-Rs)的增强作用。为了阐明其潜在机制,对非洲爪蟾卵母细胞中功能性表达的重组α(1)β(1)γ(2)GABAA受体进行了电压钳记录。在佛波酯12-肉豆蔻酸酯13-乙酸酯(PMA)孵育前后,检测GABAA-Rs对安定和PB的敏感性。PMA(25 nM)可使GABAA电流显著衰减(p<0.05,n=12-19),最高可达90%。然而,PMA处理并未改变对安定或戊巴比妥的敏感性。重组α(1)β(2)γ(2)GABAA受体也得到了类似的结果。这些数据表明,PKC激活不会改变苯二氮䓬类药物和巴比妥类药物对GABAA-Rs的变构调节,这与卵母细胞中其他研究的观察结果一致,即PMA通过受体内化而非受体动力学改变来降低GABA激活电流的幅度。