毒蕈碱乙酰胆碱受体
神经科学
乙酰胆碱受体
乙酰胆碱
心理学
毒蕈碱乙酰胆碱受体M5
毒蕈碱乙酰胆碱受体M3
医学
药理学
受体
内科学
作者
Samantha E. Yohn,Peter J. Weiden,Christian C. Felder,Stephen M. Stahl
标识
DOI:10.1016/j.tips.2022.09.006
摘要
Modern interest in muscarinic acetylcholine receptor (mAChR) activators for schizophrenia began in the 1990s when xanomeline, an M1/M4-preferring mAChR agonist developed for cognitive symptoms of Alzheimer's disease (AD), had unexpected antipsychotic activity. However, strategies to address tolerability concerns associated with activation of peripheral mAChRs were not available at that time. The discovery of specific targeted ligands and combination treatments to reduce peripheral mAChR engagement have advanced the potential of mAChR activators as effective treatments for psychotic disorders. This review provides perspectives on the background of the identification of mAChRs as potential antipsychotics, advances in the preclinical understanding of mAChRs as targets, and the current state of mAChR activators under active clinical development for schizophrenia.
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