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Overview of Glutamatergic Dysregulation in Central Pathologies

As the major excitatory neurotransmitter in the mammalian central nervous system, glutamate plays a key role in many central pathologies, including gliomas, psychiatric, neurodevelopmental, and neurodegenerative disorders. Post-mortem and serological studies have implicated glutamatergic dysregulati...

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Detalles Bibliográficos
Autores principales: Miladinovic, Tanya, Nashed, Mina G., Singh, Gurmit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693272/
https://www.ncbi.nlm.nih.gov/pubmed/26569330
http://dx.doi.org/10.3390/biom5043112
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author Miladinovic, Tanya
Nashed, Mina G.
Singh, Gurmit
author_facet Miladinovic, Tanya
Nashed, Mina G.
Singh, Gurmit
author_sort Miladinovic, Tanya
collection PubMed
description As the major excitatory neurotransmitter in the mammalian central nervous system, glutamate plays a key role in many central pathologies, including gliomas, psychiatric, neurodevelopmental, and neurodegenerative disorders. Post-mortem and serological studies have implicated glutamatergic dysregulation in these pathologies, and pharmacological modulation of glutamate receptors and transporters has provided further validation for the involvement of glutamate. Furthermore, efforts from genetic, in vitro, and animal studies are actively elucidating the specific glutamatergic mechanisms that contribute to the aetiology of central pathologies. However, details regarding specific mechanisms remain sparse and progress in effectively modulating glutamate to alleviate symptoms or inhibit disease states has been relatively slow. In this report, we review what is currently known about glutamate signalling in central pathologies. We also discuss glutamate’s mediating role in comorbidities, specifically cancer-induced bone pain and depression.
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spelling pubmed-46932722016-01-07 Overview of Glutamatergic Dysregulation in Central Pathologies Miladinovic, Tanya Nashed, Mina G. Singh, Gurmit Biomolecules Review As the major excitatory neurotransmitter in the mammalian central nervous system, glutamate plays a key role in many central pathologies, including gliomas, psychiatric, neurodevelopmental, and neurodegenerative disorders. Post-mortem and serological studies have implicated glutamatergic dysregulation in these pathologies, and pharmacological modulation of glutamate receptors and transporters has provided further validation for the involvement of glutamate. Furthermore, efforts from genetic, in vitro, and animal studies are actively elucidating the specific glutamatergic mechanisms that contribute to the aetiology of central pathologies. However, details regarding specific mechanisms remain sparse and progress in effectively modulating glutamate to alleviate symptoms or inhibit disease states has been relatively slow. In this report, we review what is currently known about glutamate signalling in central pathologies. We also discuss glutamate’s mediating role in comorbidities, specifically cancer-induced bone pain and depression. MDPI 2015-11-11 /pmc/articles/PMC4693272/ /pubmed/26569330 http://dx.doi.org/10.3390/biom5043112 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Miladinovic, Tanya
Nashed, Mina G.
Singh, Gurmit
Overview of Glutamatergic Dysregulation in Central Pathologies
title Overview of Glutamatergic Dysregulation in Central Pathologies
title_full Overview of Glutamatergic Dysregulation in Central Pathologies
title_fullStr Overview of Glutamatergic Dysregulation in Central Pathologies
title_full_unstemmed Overview of Glutamatergic Dysregulation in Central Pathologies
title_short Overview of Glutamatergic Dysregulation in Central Pathologies
title_sort overview of glutamatergic dysregulation in central pathologies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693272/
https://www.ncbi.nlm.nih.gov/pubmed/26569330
http://dx.doi.org/10.3390/biom5043112
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