Braverman Alan S, Tallarida Ronald J, Ruggieri Michael R
Department of Urology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
J Pharmacol Exp Ther. 2008 Jun;325(3):954-60. doi: 10.1124/jpet.108.137018. Epub 2008 Mar 13.
Smooth muscle contains multiple muscarinic receptor subtypes, including M2 and M3. M2 receptors outnumber M3 receptors. Based on the potency of subtype selective anticholinergics, contraction is mediated by the M3 subtype. However, results from knockout (KO) mice show that the M2 receptor mediates approximately 45% of the contractile response produced by the M3 receptor. The traditional theory of one receptor mediating a response does not allow assessment of interactions between receptors when more than one receptor participates in a response. Our study was performed using a novel analysis method based on dual receptor occupancy to determine how M2 and M3 receptor subtypes interact to mediate contraction in mouse stomach. Cumulative carbachol concentration contractile responses were determined for wild-type, M2-KO, and M3-KO stomach body smooth muscle. Using affinity constants for carbachol at M2 and M3 cholinergic receptors, the concentration values were converted to fractional receptor occupation. The resulting occupation-effect relations showed maximum effects for the M2 and M3 subtypes, respectively. These occupation-effect relations allow determination of the additive (expected) isobole based on this dual occupancy, thereby providing a curve (mathematically derived) for comparison against the experimentally derived value in wild type. The actual values determined experimentally in the wild type were not statistically significantly different from that predicted by the isobole. This confirms that the interaction between these mutually occupied receptors is additive. The new method of analysis also expands the traditional Schild theory that was based on a single receptor type to which the agonist and antagonist bind.
平滑肌含有多种毒蕈碱受体亚型,包括M2和M3。M2受体的数量超过M3受体。根据亚型选择性抗胆碱能药物的效力,收缩是由M3亚型介导的。然而,基因敲除(KO)小鼠的结果表明,M2受体介导了M3受体产生的约45%的收缩反应。当不止一种受体参与反应时,传统的一种受体介导一种反应的理论无法评估受体之间的相互作用。我们的研究采用了一种基于双受体占有率的新型分析方法,以确定M2和M3受体亚型如何相互作用来介导小鼠胃的收缩。测定了野生型、M2-KO和M3-KO胃体平滑肌对卡巴胆碱累积浓度的收缩反应。利用卡巴胆碱在M2和M3胆碱能受体上的亲和常数,将浓度值转换为受体占有率分数。所得的占有率-效应关系分别显示了M2和M3亚型的最大效应。这些占有率-效应关系允许根据这种双占有率确定相加性(预期)等效线,从而提供一条曲线(通过数学推导),以便与野生型实验得出的值进行比较。在野生型中实验测定的实际值与等效线预测的值在统计学上没有显著差异。这证实了这些相互占据的受体之间的相互作用是相加性的。这种新的分析方法也扩展了基于激动剂和拮抗剂结合的单一受体类型的传统希尔德理论。