Tayebati S K, Piergentili A, Natale D, Amenta F
Sezione di Anatomia Umana, Dipartimento di Scienze Farmacologiche e Medicina Sperimentale, Camerino, Italy.
J Auton Pharmacol. 1999 Apr;19(2):77-84. doi: 10.1046/j.1365-2680.1999.00118.x.
A protocol for predicting full agonist, partial agonist, and antagonist profiles of compounds with M2 muscarinic cholinergic receptor activity was developed using radioligand binding assay techniques with [3H]-N-methyl scopolamine (NMS) and [3H]-Oxotremorine-M (Oxo-M) as radioligands. Full muscarinic cholinergic receptor agonists such as muscarine and oxotremorine-M expressed a high agonist index (> 3000 for M1 muscarinic cholinergic receptors and > 900 for M2 muscarinic cholinergic receptor), whereas muscarinic receptor antagonists (selective or non-selective) for different receptor subtypes gave a low (0.5-10) agonist index. Functional studies performed on preparations of guinea-pig ileum and heart were consistent with radioligand binding assay experiments. The above results suggest that similarly as already established for the M1 muscarinic cholinergic receptor subtype, evaluation of the [3H]-NMS/[3H]-Oxo-M ratio may provide useful information on the profile of compounds acting at the M2 muscarinic cholinergic receptor subtype. The availability of simple and predictive techniques for the characterization of muscarinic M2 cholinergic receptor agonists, may help the identification of new compounds in therapeutic areas in which stimulation or inhibition of this receptor is desirable.
利用以[3H]-N-甲基东莨菪碱(NMS)和[3H]-氧化震颤素-M(Oxo-M)作为放射性配体的放射性配体结合测定技术,开发了一种预测具有M2毒蕈碱胆碱能受体活性的化合物的完全激动剂、部分激动剂和拮抗剂特征的方案。完全毒蕈碱胆碱能受体激动剂,如毒蕈碱和氧化震颤素-M,表现出较高的激动剂指数(M1毒蕈碱胆碱能受体大于3000,M2毒蕈碱胆碱能受体大于900),而不同受体亚型的毒蕈碱受体拮抗剂(选择性或非选择性)的激动剂指数较低(0.5 - 10)。在豚鼠回肠和心脏制剂上进行的功能研究与放射性配体结合测定实验一致。上述结果表明,与已建立的M1毒蕈碱胆碱能受体亚型情况类似,评估[3H]-NMS/[3H]-Oxo-M比值可能为作用于M2毒蕈碱胆碱能受体亚型的化合物特征提供有用信息。用于表征毒蕈碱M2胆碱能受体激动剂的简单且具有预测性的技术的可用性,可能有助于在需要刺激或抑制该受体的治疗领域中鉴定新化合物。