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A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia
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 h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992992/ https://www.ncbi.nlm.nih.gov/pubmed/36909280 http://dx.doi.org/10.3389/fncel.2023.1124333 |
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author | Dean, Brian Bakker, Geor Ueda, Hiroki R. Tobin, Andrew B. Brown, Alastair Kanaan, Richard A. A. |
author_facet | Dean, Brian Bakker, Geor Ueda, Hiroki R. Tobin, Andrew B. Brown, Alastair Kanaan, Richard A. A. |
author_sort | Dean, Brian |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9992992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99929922023-03-09 A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia Dean, Brian Bakker, Geor Ueda, Hiroki R. Tobin, Andrew B. Brown, Alastair Kanaan, Richard A. A. Front Cell Neurosci Neuroscience 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. Frontiers Media S.A. 2023-02-22 /pmc/articles/PMC9992992/ /pubmed/36909280 http://dx.doi.org/10.3389/fncel.2023.1124333 Text en Copyright © 2023 Dean, Bakker, Ueda, Tobin, Brown and Kanaan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Dean, Brian Bakker, Geor Ueda, Hiroki R. Tobin, Andrew B. Brown, Alastair Kanaan, Richard A. A. A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title | A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title_full | A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title_fullStr | A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title_full_unstemmed | A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title_short | A growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
title_sort | growing understanding of the role of muscarinic receptors in the molecular pathology and treatment of schizophrenia |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992992/ https://www.ncbi.nlm.nih.gov/pubmed/36909280 http://dx.doi.org/10.3389/fncel.2023.1124333 |
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