精神分裂症(面向对象编程)
毒蕈碱乙酰胆碱受体
神经科学
认知
变构调节
心理学
受体
变构调节剂
化学
药理学
精神科
医学
生物化学
作者
Lingsheng Fu,Yi Luo,Longyan Niu,Lin Ying,Xingru Chen,Junhao Zhang,Weifang Tang,Yadong Chen,Yu Jiao
标识
DOI:10.1016/j.bmc.2024.117728
摘要
Muscarinic acetylcholine receptors (mAChRs) play a significant role in the pathophysiology of schizophrenia. Although activating mAChRs holds potential in addressing the full range of schizophrenia symptoms, clinical application of many non-selective mAChR agonists in cognitive deficits, positive and negative symptoms is hindered by peripheral side effects (gastrointestinal disturbances and cardiovascular effects) and dosage restrictions. Ligands binding to the allosteric sites of mAChRs, particularly the M1 and M4 subtypes, demonstrate activity in improving cognitive function and amelioration of positive and negative symptoms associated with schizophrenia, enhancing our understanding of schizophrenia. The article aims to critically examine current design concepts and clinical advancements in synthesizing and designing small molecules targeting M1/M4, providing theoretical insights and empirical support for future research in this field.
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