Trzeciakowski J P
Department of Medical Pharmacology & Toxicology, Texas A&M University Health Science Center, College Station, TX 77843-1115, USA.
J Theor Biol. 1999 Jun 7;198(3):329-46. doi: 10.1006/jtbi.1999.0919.
A simple function, developed to represent the stimulus produced at the n -th step of a multistep signaling sequence, is applied to the classic model of agonist-receptor interaction. The model indicates that the relative efficacy of two agonists can be easily estimated from three experimental measures: maximal response, EC50, and apparent dissociation constant. Efficacy ratios obtained in this manner appear statistically and mathematically equivalent to those estimated with null-based methods. Enhancement of both maximal response (vertical amplification) and potency (horizontal amplification) are demonstrated to result from the interaction between highly efficacious agonists and signal transduction mechanisms. Both properties, not just relative maxima, must therefore be examined when comparing relative efficacy. Three additional generalized stimulus-response models are developed and shown to be functionally equivalent. Increasing the complexity of the function used to represent stimulus amplification does not appear to alter the conclusions derived based on the simple model of stimulus amplification. Analysis of the results also reveals a close relationship between mechanistic and operational modes of drug action, and allows operational parameters to be given mechanistic interpretation.
一个用于表示多步信号序列第n步产生的刺激的简单函数,被应用于激动剂-受体相互作用的经典模型。该模型表明,两种激动剂的相对效能可以通过三种实验测量轻松估计:最大反应、EC50和表观解离常数。以这种方式获得的效能比在统计学和数学上似乎等同于用基于零的方法估计的效能比。已证明,高效能激动剂与信号转导机制之间的相互作用会导致最大反应(垂直放大)和效能(水平放大)的增强。因此,在比较相对效能时,必须同时检查这两个属性,而不仅仅是相对最大值。还开发了另外三个广义刺激-反应模型,并证明它们在功能上是等效的。增加用于表示刺激放大的函数的复杂性似乎不会改变基于简单刺激放大模型得出的结论。对结果的分析还揭示了药物作用的机制模式和操作模式之间的密切关系,并允许对操作参数进行机理解释。