Cargando…

Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice

GABA(B) receptors are the G-protein-coupled receptors for GABA, the main inhibitory neurotransmitter in the central nervous system. Pharmacological activation of GABA(B) receptors regulates neurotransmission and neuronal excitability at pre- and postsynaptic sites. Electrophysiological activation of...

Descripción completa

Detalles Bibliográficos
Autores principales: Jurado-Parras, M. Teresa, Delgado-García, José M., Sánchez-Campusano, Raudel, Gassmann, Martin, Bettler, Bernhard, Gruart, Agnès
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743998/
https://www.ncbi.nlm.nih.gov/pubmed/26848590
http://dx.doi.org/10.1371/journal.pone.0148800
_version_ 1782414424766676992
author Jurado-Parras, M. Teresa
Delgado-García, José M.
Sánchez-Campusano, Raudel
Gassmann, Martin
Bettler, Bernhard
Gruart, Agnès
author_facet Jurado-Parras, M. Teresa
Delgado-García, José M.
Sánchez-Campusano, Raudel
Gassmann, Martin
Bettler, Bernhard
Gruart, Agnès
author_sort Jurado-Parras, M. Teresa
collection PubMed
description GABA(B) receptors are the G-protein-coupled receptors for GABA, the main inhibitory neurotransmitter in the central nervous system. Pharmacological activation of GABA(B) receptors regulates neurotransmission and neuronal excitability at pre- and postsynaptic sites. Electrophysiological activation of GABA(B) receptors in brain slices generally requires strong stimulus intensities. This raises the question as to whether behavioral stimuli are strong enough to activate GABA(B) receptors. Here we show that GABA(B1a)(-/-) mice, which constitutively lack presynaptic GABA(B) receptors at glutamatergic synapses, are impaired in their ability to acquire an operant learning task. In vivo recordings during the operant conditioning reveal a deficit in learning-dependent increases in synaptic strength at CA3-CA1 synapses. Moreover, GABA(B1a)(-/-) mice fail to synchronize neuronal activity in the CA1 area during the acquisition process. Our results support that activation of presynaptic hippocampal GABA(B) receptors is important for acquisition of a learning task and for learning-associated synaptic changes and network dynamics.
format Online
Article
Text
id pubmed-4743998
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-47439982016-02-11 Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice Jurado-Parras, M. Teresa Delgado-García, José M. Sánchez-Campusano, Raudel Gassmann, Martin Bettler, Bernhard Gruart, Agnès PLoS One Research Article GABA(B) receptors are the G-protein-coupled receptors for GABA, the main inhibitory neurotransmitter in the central nervous system. Pharmacological activation of GABA(B) receptors regulates neurotransmission and neuronal excitability at pre- and postsynaptic sites. Electrophysiological activation of GABA(B) receptors in brain slices generally requires strong stimulus intensities. This raises the question as to whether behavioral stimuli are strong enough to activate GABA(B) receptors. Here we show that GABA(B1a)(-/-) mice, which constitutively lack presynaptic GABA(B) receptors at glutamatergic synapses, are impaired in their ability to acquire an operant learning task. In vivo recordings during the operant conditioning reveal a deficit in learning-dependent increases in synaptic strength at CA3-CA1 synapses. Moreover, GABA(B1a)(-/-) mice fail to synchronize neuronal activity in the CA1 area during the acquisition process. Our results support that activation of presynaptic hippocampal GABA(B) receptors is important for acquisition of a learning task and for learning-associated synaptic changes and network dynamics. Public Library of Science 2016-02-05 /pmc/articles/PMC4743998/ /pubmed/26848590 http://dx.doi.org/10.1371/journal.pone.0148800 Text en © 2016 Jurado-Parras et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jurado-Parras, M. Teresa
Delgado-García, José M.
Sánchez-Campusano, Raudel
Gassmann, Martin
Bettler, Bernhard
Gruart, Agnès
Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title_full Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title_fullStr Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title_full_unstemmed Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title_short Presynaptic GABA(B) Receptors Regulate Hippocampal Synapses during Associative Learning in Behaving Mice
title_sort presynaptic gaba(b) receptors regulate hippocampal synapses during associative learning in behaving mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743998/
https://www.ncbi.nlm.nih.gov/pubmed/26848590
http://dx.doi.org/10.1371/journal.pone.0148800
work_keys_str_mv AT juradoparrasmteresa presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice
AT delgadogarciajosem presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice
AT sanchezcampusanoraudel presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice
AT gassmannmartin presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice
AT bettlerbernhard presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice
AT gruartagnes presynapticgababreceptorsregulatehippocampalsynapsesduringassociativelearninginbehavingmice