Ghansah E, Weiss D S
Department of Neurobiology, The University of Alabama at Birmingham, School of Medicine, 35294-0021, USA.
Neuroreport. 1999 Mar 17;10(4):817-21. doi: 10.1097/00001756-199903170-00028.
Previous studies suggest that diazepam (DZP) increases the desensitization rate of GABA(A) receptors, although this effect could simply be a consequence of the DZP-induced increase in GABA sensitivity rather than a direct modulation of desensitization kinetics. To distinguish these two possibilities, voltage clamp recordings were performed on rat alpha1beta2gamma2 GABA(A) receptors expressed in Xenopus laevis oocytes. Complete GABA concentration-response relationships were obtained in the absence and presence of 1 microM DZP and the observed shift in GABA sensitivity (approximately 2.5-fold) was used to adjust GABA and GABA plus DZP to the same level of activation. In this case, DZP had no significant effect on either the rate of onset or recovery from desensitization. This suggests that the apparent effect of DZP on the rate of desensitization is secondary to the increase in GABA sensitivity and not due to a direct effect on the process of desensitization.
先前的研究表明,地西泮(DZP)会提高GABA(A)受体的脱敏率,尽管这种效应可能仅仅是DZP诱导的GABA敏感性增加的结果,而非对脱敏动力学的直接调节。为了区分这两种可能性,对非洲爪蟾卵母细胞中表达的大鼠α1β2γ2 GABA(A)受体进行了电压钳记录。在不存在和存在1 microM DZP的情况下获得了完整的GABA浓度-反应关系,并利用观察到的GABA敏感性变化(约2.5倍)将GABA以及GABA加DZP调整到相同的激活水平。在这种情况下,DZP对脱敏的起始速率或恢复速率均无显著影响。这表明DZP对脱敏速率的明显作用是GABA敏感性增加的继发效应,而非对脱敏过程的直接作用。