Leff P, Martin G R, Morse J M
Br J Pharmacol. 1985 Jul;85(3):655-63. doi: 10.1111/j.1476-5381.1985.tb10561.x.
The operational model of agonism (Black & Leff, 1983) has been used to analyse comparatively functional antagonism and irreversible antagonism as methods for estimating agonist dissociation constants (KAs). A general condition is established in terms of the model parameters which defines the type of experimental interventions at the receptor and the post-receptor level that allow valid KA estimation. It is shown that functional antagonism and other post-receptor interventions may produce changes in agonist-concentration effect curves which are qualitatively indistinguishable but quantitatively distinct, from those produced by irreversible antagonism. Experimental data obtained with the guinea-pig tracheal strip preparation are in keeping with the theoretical predictions and show how studies using functional antagonism may overestimate agonist affinity. In general, functional antagonism, unlike irreversible antagonism, is in principle an unreliable method for quantifying agonism.
激动作用的操作模型(布莱克和莱夫,1983年)已被用于比较分析功能性拮抗和不可逆拮抗,作为估计激动剂解离常数(KAs)的方法。根据模型参数建立了一个一般条件,该条件定义了在受体和受体后水平上允许有效估计KA的实验干预类型。结果表明,功能性拮抗和其他受体后干预可能会使激动剂浓度效应曲线产生变化,这些变化在定性上与不可逆拮抗产生的变化无法区分,但在定量上有所不同。用豚鼠气管条制备获得的实验数据与理论预测一致,并表明使用功能性拮抗的研究可能会高估激动剂亲和力。一般来说,与不可逆拮抗不同,功能性拮抗原则上是一种不可靠的激动作用量化方法。