Takai Kentaro, Enomoto Takeshi
Drug Research Division, Sumitomo Dainippon Pharma Co., Ltd.
Chem Pharm Bull (Tokyo). 2018;66(1):37-44. doi: 10.1248/cpb.c17-00413.
Among the muscarinic acetylcholine receptor (mAChR) subtypes, the M receptor has been investigated as a promising drug target for the treatment of schizophrenia. These investigations have been based on findings from M-deficient mice studies as well as on the results of a clinical trial that used xanomeline, an M/M mAChRs-preferring agonist. Both orthosteric agonists and positive allosteric modulators of M mAChR have been reported as promising ligands that not only have antipsychotic effects, but can also improve cognitive impairment and motor dysfunction. However, challenges remain due to the high homology of the orthosteric binding site among all muscarinic receptors. In this review, we summarize our approach to the identification of M mAChR activators, orthosteric agonists, and positive allosteric modulators based on M mAChR structural information and structure-activity relationship studies. These findings indicate that selective M mAChR activators are promising potential therapeutic agents for several central nervous system conditions.
在毒蕈碱型乙酰胆碱受体(mAChR)亚型中,M受体已被作为治疗精神分裂症的一个有前景的药物靶点进行研究。这些研究基于M缺陷小鼠研究的结果以及一项使用xanomeline(一种优先作用于M/M mAChRs的激动剂)的临床试验结果。M mAChR的正构激动剂和正变构调节剂均被报道为有前景的配体,它们不仅具有抗精神病作用,还能改善认知障碍和运动功能障碍。然而,由于所有毒蕈碱受体中正构结合位点的高度同源性,挑战依然存在。在本综述中,我们总结了基于M mAChR结构信息和构效关系研究来鉴定M mAChR激活剂、正构激动剂和正变构调节剂的方法。这些发现表明,选择性M mAChR激活剂对于几种中枢神经系统疾病是有前景的潜在治疗药物。