Targeting Muscarinic Acetylcholine Receptors for the Treatment of Psychiatric and Neurological Disorders

被引:100
作者
Moran, Sean P. [1 ,2 ,3 ]
Maksymetz, James [2 ,3 ]
Conn, P. Jeffrey [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Vanderbilt Brain Inst, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Ctr Neurosci Drug Discovery, Nashville, TN 37232 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
POSITIVE ALLOSTERIC MODULATORS; VIVO TOOL COMPOUND; M-4; RECEPTOR; AGONIST; M1; DOPAMINE; XANOMELINE; PAM; RAT; CNS;
D O I
10.1016/j.tips.2019.10.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Muscarinic acetylcholine receptors (mAChR) play important roles in regulating complex behaviors such as cognition, movement, and reward, making them ideally situated as potential drug targets for the treatment of several brain disorders. Recent advances in the discovery of subtype-selective allosteric modulators for mAChRs has provided an unprecedented opportunity for highly specific modulation of signaling by individual mAChR subtypes in the brain Recently, mAChR allosteric modulators have entered clinical development for Alzheimer's disease (AD) and schizophrenia, and have potential utility for other brain disorders. However, mAChR allosteric modulators can display a diverse array of pharmacological properties, and a more nuanced understanding of the mAChR will be necessary to best translate predinical findings into successful clinical treatments.
引用
收藏
页码:1006 / 1020
页数:15
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