Henry P J, Lulich K M, Paterson J W
Br J Pharmacol. 1985 Sep;86(1):131-9. doi: 10.1111/j.1476-5381.1985.tb09443.x.
Several key predictions of a recently developed model for functional antagonism (Mackay, 1981) were experimentally tested using the rat isolated costo-uterine preparation. In the presence of the functional antagonist fenoterol (Fen), the functional constants (KAF) for carbachol and oxotremorine (Oxo) were respectively 9.9 and 3.4 fold greater than their corresponding affinity constants (KA). According to Mackay's model for functional antagonism, the higher KAF/KA ratio for carbachol indicates that this cholinoceptor agonist has a greater efficacy than Oxo. This was confirmed by using conventional pharmacological methods. As predicted from the model of functional antagonism, the plot of KAF/KA-1 against the fraction of cholinoceptors not irreversibly blocked by phenoxybenzamine (Pbz) was linear for both carbachol and Oxo and the lines of best fit crossed the axes at a point not significantly different from the origin. The value of 4.6 for the relative efficacy of carbachol to Oxo estimated from functional antagonism studies was comparable to the value of 5.6 calculated using the method of irreversible antagonism proposed by Furchgott (1966).
使用大鼠离体肋-子宫制备物对最近开发的功能拮抗模型(麦凯,1981年)的几个关键预测进行了实验测试。在功能拮抗剂非诺特罗(Fen)存在的情况下,卡巴胆碱和氧化震颤素(Oxo)的功能常数(KAF)分别比其相应的亲和常数(KA)大9.9倍和3.4倍。根据麦凯的功能拮抗模型,卡巴胆碱的KAF/KA比值较高表明该胆碱能受体激动剂比氧化震颤素有更高的效能。这通过传统药理学方法得到了证实。正如功能拮抗模型所预测的那样,卡巴胆碱和氧化震颤素的KAF/KA - 1对未被苯氧苄胺(Pbz)不可逆阻断的胆碱能受体分数的作图均为线性,且最佳拟合线与坐标轴的交点与原点无显著差异。从功能拮抗研究估计的卡巴胆碱对氧化震颤素的相对效能值4.6与使用弗奇戈特(1966年)提出的不可逆拮抗方法计算的5.6值相当。