Celentano J J, Wong R K
Department of Pharmacology, State University of New York Health Science Center, Brooklyn 11203.
Biophys J. 1994 Apr;66(4):1039-50. doi: 10.1016/S0006-3495(94)80885-9.
GABAA receptor function was studied in outside-out patches from guinea pig hippocampal neurons using a drug application system with an exchange time of under 1.5 ms. Application of GABA to these patches induced a Cl- conductance that desensitized with prolonged exposure. Increasing GABA concentrations induced larger conductance increases that were associated with more complex patterns of desensitization. Smaller GABA responses desensitized with monophasic kinetics, whereas large responses displayed bi- and triphasic kinetics. Desensitization of the response to 1 mM GABA was triphasic in about 70% of the patches (tau = 15.4, 207, and 1370 ms) and biphasic in about 30% of the patches (tau = 44 and 725 ms). All phases of desensitization reversed at the Cl- equilibrium potential. Over the concentration range from 3 microM to 3 mM, both the rate and the extent of desensitization increased; however, complete desensitization was rarely observed. The increase in desensitization rate was due to an increase in the relative contribution of the faster phases with increasing GABA. The time constants of the three phases were independent of concentration. The different phases are not mediated by separate receptor populations, because double pulse experiments demonstrated interconversion among the fastest phase and the two slower phases. We demonstrate the plausibility of a model in which multiphasic desensitization is a consequence of the faster association rate at higher GABA concentrations.
利用交换时间在1.5毫秒以下的药物施加系统,对豚鼠海马神经元的外向型膜片进行了GABAA受体功能研究。向这些膜片施加GABA可诱导氯离子电导,该电导会随着暴露时间延长而脱敏。增加GABA浓度会诱导更大的电导增加,且与更复杂的脱敏模式相关。较小的GABA反应以单相动力学脱敏,而较大的反应则表现出双相和三相动力学。对1 mM GABA反应的脱敏在约70%的膜片中为三相(时间常数分别为15.4、207和1370毫秒),在约30%的膜片中为双相(时间常数分别为44和725毫秒)。脱敏的所有阶段在氯离子平衡电位处均会逆转。在3 microM至3 mM的浓度范围内,脱敏的速率和程度均增加;然而,很少观察到完全脱敏。脱敏速率的增加是由于随着GABA浓度增加,较快阶段的相对贡献增加。三个阶段的时间常数与浓度无关。不同阶段并非由不同的受体群体介导,因为双脉冲实验表明最快阶段与两个较慢阶段之间可相互转换。我们证明了一个模型的合理性,即多相脱敏是较高GABA浓度下更快结合速率的结果。