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对毒蕈碱受体在精神分裂症分子病理学及治疗中作用的认识不断加深。

A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia.

作者信息

Dean Brian, Bakker Geor, Ueda Hiroki R, Tobin Andrew B, Brown Alastair, Kanaan Richard A A

机构信息

Synaptic Biology and Cognition Laboratory, The Florey Institute of Neuroscience and Mental Health, Parkville, VIC, Australia.

Sosei Heptares, Cambridge, United Kingdom.

出版信息

Front Cell Neurosci. 2023 Feb 22;17:1124333. doi: 10.3389/fncel.2023.1124333. eCollection 2023.

Abstract

Pre-clinical models, postmortem and neuroimaging studies all support a role for muscarinic receptors in the molecular pathology of schizophrenia. From these data it was proposed that activation of the muscarinic M1 and/or M4 receptor would reduce the severity of the symptoms of schizophrenia. This hypothesis is now supported by results from two clinical trials which indicate that activating central muscarinic M1 and M4 receptors can reduce the severity of positive, negative and cognitive symptoms of the disorder. This review will provide an update on a growing body of evidence that argues the muscarinic M1 and M4 receptors have critical roles in CNS functions that are dysregulated by the pathophysiology of schizophrenia. This realization has been made possible, in part, by the growing ability to visualize and quantify muscarinic M1 and M4 receptors in the human CNS using molecular neuroimaging. We will discuss how these advances have provided evidence to support the notion that there is a sub-group of patients within the syndrome of schizophrenia that have a unique molecular pathology driven by a marked loss of muscarinic M1 receptors. This review is timely, as drugs targeting muscarinic receptors approach clinical use for the treatment of schizophrenia and here we outline the background biology that supported development of such drugs to treat the disorder.

摘要

临床前模型、尸检和神经影像学研究均支持毒蕈碱受体在精神分裂症分子病理学中的作用。基于这些数据,有人提出激活毒蕈碱M1和/或M4受体可减轻精神分裂症症状的严重程度。目前,两项临床试验的结果支持了这一假设,即激活中枢毒蕈碱M1和M4受体可减轻该疾病的阳性、阴性和认知症状的严重程度。本综述将更新越来越多的证据,这些证据表明毒蕈碱M1和M4受体在中枢神经系统功能中起关键作用,而这些功能在精神分裂症的病理生理学过程中失调。这一认识的达成,部分得益于利用分子神经影像学在人类中枢神经系统中可视化和量化毒蕈碱M1和M4受体的能力不断提高。我们将讨论这些进展如何为支持以下观点提供了证据:在精神分裂症综合征患者中有一个亚组,其具有由毒蕈碱M1受体显著丧失驱动的独特分子病理学。鉴于靶向毒蕈碱受体的药物即将用于精神分裂症的临床治疗,本综述恰逢其时,在此我们概述了支持开发此类药物治疗该疾病的背景生物学知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afd5/9992992/5cc95bbbb764/fncel-17-1124333-g001.jpg

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