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Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System
Group I metabotropic glutamate (mGlu) receptors consists of mGlu1 and mGlu5 receptor subtypes. These receptors are widely distributed in the central nervous system (CNS), where they preferentially mediate facilitatory signaling in neurones and glial cells, mainly by favoring phospholipase (PLC) tran...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006178/ https://www.ncbi.nlm.nih.gov/pubmed/27630571 http://dx.doi.org/10.3389/fphar.2016.00295 |
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author | Pittaluga, Anna |
author_facet | Pittaluga, Anna |
author_sort | Pittaluga, Anna |
collection | PubMed |
description | Group I metabotropic glutamate (mGlu) receptors consists of mGlu1 and mGlu5 receptor subtypes. These receptors are widely distributed in the central nervous system (CNS), where they preferentially mediate facilitatory signaling in neurones and glial cells, mainly by favoring phospholipase (PLC) translocation. Based on the literature so far available, group I Metabotropic glutamate receptors (mGluRs) are preferentially expressed at the postsynaptic side of chemical synapsis, where they participate in the progression of the chemical stimulus. Studies, however, have shown the presence of these receptors also at the presynaptic level, where they exert several functions, including the modulation of transmitter exocytosis. Presynaptic Group I mGluRs can be both autoreceptors regulating release of glutamate and heteroreceptors regulating the release of various transmitters, including GABA, dopamine, noradrenaline, and acetylcholine. While the existence of presynaptic release-regulating mGlu5 receptors is largely recognized, the possibility that mGlu1 receptors also are present at this level has been a matter of discussion for a long time. A large body of evidence published in the last decade, however, supports this notion. This review aims at revisiting the data from in vitro studies concerning the existence and the role of release-regulating mGlu1 receptors presynaptically located in nerve terminals isolated from selected regions of the CNS. The functional interaction linking mGlu5 and mGlu1 receptor subtypes at nerve terminals and their relative contributions as modulators of central transmission will also be discussed. We apologize in advance for omission in our coverage of the existing literature. |
format | Online Article Text |
id | pubmed-5006178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50061782016-09-14 Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System Pittaluga, Anna Front Pharmacol Pharmacology Group I metabotropic glutamate (mGlu) receptors consists of mGlu1 and mGlu5 receptor subtypes. These receptors are widely distributed in the central nervous system (CNS), where they preferentially mediate facilitatory signaling in neurones and glial cells, mainly by favoring phospholipase (PLC) translocation. Based on the literature so far available, group I Metabotropic glutamate receptors (mGluRs) are preferentially expressed at the postsynaptic side of chemical synapsis, where they participate in the progression of the chemical stimulus. Studies, however, have shown the presence of these receptors also at the presynaptic level, where they exert several functions, including the modulation of transmitter exocytosis. Presynaptic Group I mGluRs can be both autoreceptors regulating release of glutamate and heteroreceptors regulating the release of various transmitters, including GABA, dopamine, noradrenaline, and acetylcholine. While the existence of presynaptic release-regulating mGlu5 receptors is largely recognized, the possibility that mGlu1 receptors also are present at this level has been a matter of discussion for a long time. A large body of evidence published in the last decade, however, supports this notion. This review aims at revisiting the data from in vitro studies concerning the existence and the role of release-regulating mGlu1 receptors presynaptically located in nerve terminals isolated from selected regions of the CNS. The functional interaction linking mGlu5 and mGlu1 receptor subtypes at nerve terminals and their relative contributions as modulators of central transmission will also be discussed. We apologize in advance for omission in our coverage of the existing literature. Frontiers Media S.A. 2016-08-31 /pmc/articles/PMC5006178/ /pubmed/27630571 http://dx.doi.org/10.3389/fphar.2016.00295 Text en Copyright © 2016 Pittaluga. 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) or licensor 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 | Pharmacology Pittaluga, Anna Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title | Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title_full | Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title_fullStr | Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title_full_unstemmed | Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title_short | Presynaptic Release-Regulating mGlu1 Receptors in Central Nervous System |
title_sort | presynaptic release-regulating mglu1 receptors in central nervous system |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006178/ https://www.ncbi.nlm.nih.gov/pubmed/27630571 http://dx.doi.org/10.3389/fphar.2016.00295 |
work_keys_str_mv | AT pittalugaanna presynapticreleaseregulatingmglu1receptorsincentralnervoussystem |