Department of Anesthesiology (ALG, SRP, ASE, JHS, GA), Washington University School of Medicine, St. Louis, MO 63110,United States.
Department of Anesthesiology (ALG, SRP, ASE, JHS, GA), Washington University School of Medicine, St. Louis, MO 63110,United States | The Taylor Family Institute for Innovative Psychiatric Research, Washington University School of Medicine, St. Louis, MO 63110, USA.
Curr Neuropharmacol. 2022;20(1):90-93. doi: 10.2174/1570159X19666211104142433.
In electrophysiological experiments, inhibition of a receptor-channel, such as the GABAA receptor, is measured by co-applying an agonist producing a predefined control response with an inhibitor to calculate the fraction of the control response remaining in the presence of the inhibitor. The properties of the inhibitor are determined by fitting the inhibition concentration- response relationship to the Hill equation to estimate the midpoint (IC50) of the inhibition curve Objective: We sought to estimate sensitivity of the fitted IC50 to the level of activity of the control response Methods: The inhibition concentration-response relationships were calculated for models with distinct mechanisms of inhibition. In Model I, the inhibitor acts allosterically to stabilize the resting state of the receptor. In Model II, the inhibitor competes with the agonist for a shared binding site. In Model III, the inhibitor stabilizes the desensitized state.
The simulations indicate that the fitted IC50 of the inhibition curve is sensitive to the degree of activity of the control response. In Models I and II, the IC50 of inhibition was increased as the probability of being in the active state (PA) of the control response increased. In Model III, the IC50 of inhibition was reduced at higher PA.
We infer that the apparent potency of an inhibitor depends on the PA of the control response. While the calculations were carried out using the activation and inhibition properties that are representative of the GABAA receptor, the principles and conclusions apply to a wide variety of receptor- channels.
在电生理学实验中,通过同时应用激动剂产生预定义的对照反应和抑制剂来测量受体-通道(如 GABA A 受体)的抑制作用,从而计算出在抑制剂存在下对照反应剩余的分数。抑制剂的特性通过将抑制浓度-反应关系拟合到 Hill 方程来确定,以估计抑制曲线的中点(IC50)。
我们旨在估计拟合的 IC50 对对照反应活性水平的敏感性。
为具有不同抑制机制的模型计算了抑制浓度-反应关系。在模型 I 中,抑制剂作为变构调节剂作用,稳定受体的静息状态。在模型 II 中,抑制剂与激动剂竞争共享结合位点。在模型 III 中,抑制剂稳定脱敏状态。
模拟结果表明,抑制曲线的拟合 IC50 对对照反应的活性水平敏感。在模型 I 和 II 中,随着对照反应的活性状态(PA)概率的增加,抑制的 IC50 增加。在模型 III 中,抑制的 IC50 在较高的 PA 时降低。
我们推断抑制剂的表观效力取决于对照反应的 PA。虽然计算是使用代表 GABA A 受体的激活和抑制特性进行的,但这些原理和结论适用于广泛的受体-通道。