Van Cauter E, Hardman J G, Dumont J E
Proc Natl Acad Sci U S A. 1976 Sep;73(9):2982-6. doi: 10.1073/pnas.73.9.2982.
Mediators of hormone and neurotransmitter action may exert negative control on the accumulation of one another (adenosine 3':5'-cyclic monophosphate, or conversely). A model in which one agonist stimulates the formation of two mediators which inhibit each other's accumulation has been simulated. Three types of agonist-receptor interaction, five mechanisms of inhibition, and three types of basal activity have been considered which lead to a set of 45 descriptions of the general cross inhibition model. For these submodels, pattern of the relation of agonist to mediator concentrations at steady state conditions have been defined. Some patterns are complex with mediator curves exhibiting extrema, one a maximum and the other a minimum. The complexity of the pattern depends on the submodel and on the degree of asymmetry between the parameters of each of the mediator pathways (e.g.,affinities for the agonist, strength of the inhibitions, etc.). This simple model can thus account for complex experimental results without requiring the postulation of elaborate molecular models of agonist-receptor interaction. The simulations presented emphasize the necessity of investigating a wide range of agonist concentrations.
激素和神经递质作用的介质可能会对彼此的积累产生负调控(例如3':5'-环磷酸腺苷,反之亦然)。已模拟了一种模型,其中一种激动剂刺激形成两种相互抑制积累的介质。考虑了三种类型的激动剂-受体相互作用、五种抑制机制和三种基础活性类型,这导致了一组45种对一般交叉抑制模型的描述。对于这些子模型,已定义了稳态条件下激动剂与介质浓度关系的模式。一些模式很复杂,介质曲线呈现极值,一个是最大值,另一个是最小值。模式的复杂性取决于子模型以及每个介质途径参数之间的不对称程度(例如,对激动剂的亲和力、抑制强度等)。因此,这个简单的模型可以解释复杂的实验结果,而无需假设复杂的激动剂-受体相互作用分子模型。所展示的模拟强调了研究广泛的激动剂浓度范围的必要性。