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Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders
Neurodevelopmental disorders (NDDs) are characterized by a wide range of symptoms including delayed speech, intellectual disability, motor dysfunction, social deficits, breathing problems, structural abnormalities, and epilepsy. Unfortunately, current treatment strategies are limited and innovative...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206046/ https://www.ncbi.nlm.nih.gov/pubmed/30405350 http://dx.doi.org/10.3389/fnmol.2018.00387 |
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author | Fisher, Nicole M. Seto, Mabel Lindsley, Craig W. Niswender, Colleen M. |
author_facet | Fisher, Nicole M. Seto, Mabel Lindsley, Craig W. Niswender, Colleen M. |
author_sort | Fisher, Nicole M. |
collection | PubMed |
description | Neurodevelopmental disorders (NDDs) are characterized by a wide range of symptoms including delayed speech, intellectual disability, motor dysfunction, social deficits, breathing problems, structural abnormalities, and epilepsy. Unfortunately, current treatment strategies are limited and innovative new approaches are sorely needed to address these complex diseases. The metabotropic glutamate receptors are a class of G protein-coupled receptors that act to modulate neurotransmission across many brain structures. They have shown great promise as drug targets for numerous neurological and psychiatric diseases. Moreover, the development of subtype-selective allosteric modulators has allowed detailed studies of each receptor subtype. Here, we focus on the metabotropic glutamate receptor 7 (mGlu(7)) as a potential therapeutic target for NDDs. mGlu(7) is expressed widely throughout the brain in regions that correspond to the symptom domains listed above and has established roles in synaptic physiology and behavior. Single nucleotide polymorphisms and mutations in the GRM7 gene have been associated with idiopathic autism and other NDDs in patients. In rodent models, existing literature suggests that decreased mGlu(7) expression and/or function may lead to symptoms that overlap with those of NDDs. Furthermore, potentiation of mGlu(7) activity has shown efficacy in a mouse model of Rett syndrome. In this review, we summarize current findings that provide rationale for the continued development of mGlu(7) modulators as potential therapeutics. |
format | Online Article Text |
id | pubmed-6206046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62060462018-11-07 Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders Fisher, Nicole M. Seto, Mabel Lindsley, Craig W. Niswender, Colleen M. Front Mol Neurosci Molecular Neuroscience Neurodevelopmental disorders (NDDs) are characterized by a wide range of symptoms including delayed speech, intellectual disability, motor dysfunction, social deficits, breathing problems, structural abnormalities, and epilepsy. Unfortunately, current treatment strategies are limited and innovative new approaches are sorely needed to address these complex diseases. The metabotropic glutamate receptors are a class of G protein-coupled receptors that act to modulate neurotransmission across many brain structures. They have shown great promise as drug targets for numerous neurological and psychiatric diseases. Moreover, the development of subtype-selective allosteric modulators has allowed detailed studies of each receptor subtype. Here, we focus on the metabotropic glutamate receptor 7 (mGlu(7)) as a potential therapeutic target for NDDs. mGlu(7) is expressed widely throughout the brain in regions that correspond to the symptom domains listed above and has established roles in synaptic physiology and behavior. Single nucleotide polymorphisms and mutations in the GRM7 gene have been associated with idiopathic autism and other NDDs in patients. In rodent models, existing literature suggests that decreased mGlu(7) expression and/or function may lead to symptoms that overlap with those of NDDs. Furthermore, potentiation of mGlu(7) activity has shown efficacy in a mouse model of Rett syndrome. In this review, we summarize current findings that provide rationale for the continued development of mGlu(7) modulators as potential therapeutics. Frontiers Media S.A. 2018-10-23 /pmc/articles/PMC6206046/ /pubmed/30405350 http://dx.doi.org/10.3389/fnmol.2018.00387 Text en Copyright © 2018 Fisher, Seto, Lindsley and Niswender. http://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 | Molecular Neuroscience Fisher, Nicole M. Seto, Mabel Lindsley, Craig W. Niswender, Colleen M. Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title | Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title_full | Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title_fullStr | Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title_full_unstemmed | Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title_short | Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders |
title_sort | metabotropic glutamate receptor 7: a new therapeutic target in neurodevelopmental disorders |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206046/ https://www.ncbi.nlm.nih.gov/pubmed/30405350 http://dx.doi.org/10.3389/fnmol.2018.00387 |
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