Chou T C, Talalay P
Adv Enzyme Regul. 1984;22:27-55. doi: 10.1016/0065-2571(84)90007-4.
A generalized method for analyzing the effects of multiple drugs and for determining summation, synergism and antagonism has been proposed. The derived, generalized equations are based on kinetic principles. The method is relatively simple and is not limited by whether the dose-effect relationships are hyperbolic or sigmoidal, whether the effects of the drugs are mutually exclusive or nonexclusive, whether the ligand interactions are competitive, noncompetitive or uncompetitive, whether the drugs are agonists or antagonists, or the number of drugs involved. The equations for the two most widely used methods for analyzing synergism, antagonism and summation of effects of multiple drugs, the isobologram and fractional product concepts, have been derived and been shown to have limitations in their applications. These two methods cannot be used indiscriminately. The equations underlying these two methods can be derived from a more generalized equation previously developed by us (59). It can be shown that the isobologram is valid only for drugs whose effects are mutually exclusive, whereas the fractional product method is valid only for mutually nonexclusive drugs which have hyperbolic dose-effect curves. Furthermore, in the isobol method, it is laborious to find proper combinations of drugs that would produce an iso-effective curve, and the fractional product method tends to give indication of synergism, since it underestimates the summation of the effect of mutually nonexclusive drugs that have sigmoidal dose-effect curves. The method described herein is devoid of these deficiencies and limitations. The simplified experimental design proposed for multiple drug-effect analysis has the following advantages: It provides a simple diagnostic plot (i.e., the median-effect plot) for evaluating the applicability of the data, and provides parameters that can be directly used to obtain a general equation for the dose-effect relation; the analysis which involves logarithmic conversion and linear regression can be readily carried out with a simple programmable electronic calculator and does not require special graph paper or tables; and the simplicity of the equation allows flexibility of application and the use of a minimum number of data points. This method has been used to analyze experimental data obtained from enzymatic, cellular and animal systems.
已经提出了一种用于分析多种药物的作用以及确定相加、协同和拮抗作用的通用方法。推导得出的通用方程基于动力学原理。该方法相对简单,不受剂量-效应关系是双曲线型还是S型、药物作用是否相互排斥或非相互排斥、配体相互作用是竞争性、非竞争性还是非竞争性、药物是激动剂还是拮抗剂,以及所涉及药物的数量的限制。两种最广泛用于分析多种药物作用的相加、协同和拮抗作用的方法,即等效应线图和分数乘积概念的方程,已经推导出来,并已证明在其应用中存在局限性。这两种方法不能随意使用。这两种方法所依据的方程可以从我们先前推导的一个更通用的方程(59)中得出。可以证明,等效应线图仅对作用相互排斥的药物有效,而分数乘积法仅对具有双曲线剂量-效应曲线的非相互排斥药物有效。此外,在等效应线法中,找到能产生等效应曲线的合适药物组合很费力,而分数乘积法往往会给出协同作用的指示,因为它低估了具有S型剂量-效应曲线的非相互排斥药物作用的相加。本文所述的方法没有这些缺陷和局限性。为多种药物效应分析提出的简化实验设计具有以下优点:它提供了一个简单的诊断图(即中位效应图)来评估数据的适用性,并提供了可以直接用于获得剂量-效应关系通用方程的参数;涉及对数转换和线性回归的分析可以用简单的可编程电子计算器轻松进行,不需要特殊的图纸或表格;方程的简单性允许灵活应用并使用最少的数据点。该方法已用于分析从酶、细胞和动物系统获得的实验数据。