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Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex
Excitatory synaptic transmission in central synapses is modulated by serotonin (5-HT). The anterior cingulate cortex (ACC) is an important cortical region for pain perception and emotion. ACC neurons receive innervation of projecting serotonergic nerve terminals from raphe nuclei, but the possible e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468981/ https://www.ncbi.nlm.nih.gov/pubmed/28606116 http://dx.doi.org/10.1186/s13041-017-0303-1 |
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author | Tian, Zhen Yamanaka, Manabu Bernabucci, Matteo Zhao, Ming-gao Zhuo, Min |
author_facet | Tian, Zhen Yamanaka, Manabu Bernabucci, Matteo Zhao, Ming-gao Zhuo, Min |
author_sort | Tian, Zhen |
collection | PubMed |
description | Excitatory synaptic transmission in central synapses is modulated by serotonin (5-HT). The anterior cingulate cortex (ACC) is an important cortical region for pain perception and emotion. ACC neurons receive innervation of projecting serotonergic nerve terminals from raphe nuclei, but the possible effect of 5-HT on excitatory transmission in the ACC has not been investigated. In the present study, we investigated the role of 5-HT on glutamate neurotransmission in the ACC slices of adult mice. Bath application of 5-HT produced dose-dependent inhibition of evoked excitatory postsynaptic currents (eEPSCs). Paired pulse ratio (PPR) was significantly increased, indicating possible presynaptic effects of 5-HT. Consistently, bath application of 5-HT significantly decreased the frequency of spontaneous and miniature excitatory postsynaptic currents (sEPSCs and mEPSCs). By contrast, amplitudes of sEPSCs and mEPSCs were not significantly affected. After postsynaptic application of G protein inhibitor GDP-β-S, 5-HT produced inhibition of eEPSCs was significantly reduced. Finally, NAN-190, an antagonist of 5-HT(1A) receptor, significantly reduced postsynaptic inhibition of 5-HT and abolished presynaptic inhibition. Our results strongly suggest that presynaptic as well as postsynaptic 5-HT receptor including 5-HT1A subtype receptor may contribute to inhibitory modulation of glutamate release as well as postsynaptic responses in the ACC. |
format | Online Article Text |
id | pubmed-5468981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54689812017-06-14 Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex Tian, Zhen Yamanaka, Manabu Bernabucci, Matteo Zhao, Ming-gao Zhuo, Min Mol Brain Research Excitatory synaptic transmission in central synapses is modulated by serotonin (5-HT). The anterior cingulate cortex (ACC) is an important cortical region for pain perception and emotion. ACC neurons receive innervation of projecting serotonergic nerve terminals from raphe nuclei, but the possible effect of 5-HT on excitatory transmission in the ACC has not been investigated. In the present study, we investigated the role of 5-HT on glutamate neurotransmission in the ACC slices of adult mice. Bath application of 5-HT produced dose-dependent inhibition of evoked excitatory postsynaptic currents (eEPSCs). Paired pulse ratio (PPR) was significantly increased, indicating possible presynaptic effects of 5-HT. Consistently, bath application of 5-HT significantly decreased the frequency of spontaneous and miniature excitatory postsynaptic currents (sEPSCs and mEPSCs). By contrast, amplitudes of sEPSCs and mEPSCs were not significantly affected. After postsynaptic application of G protein inhibitor GDP-β-S, 5-HT produced inhibition of eEPSCs was significantly reduced. Finally, NAN-190, an antagonist of 5-HT(1A) receptor, significantly reduced postsynaptic inhibition of 5-HT and abolished presynaptic inhibition. Our results strongly suggest that presynaptic as well as postsynaptic 5-HT receptor including 5-HT1A subtype receptor may contribute to inhibitory modulation of glutamate release as well as postsynaptic responses in the ACC. BioMed Central 2017-06-12 /pmc/articles/PMC5468981/ /pubmed/28606116 http://dx.doi.org/10.1186/s13041-017-0303-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tian, Zhen Yamanaka, Manabu Bernabucci, Matteo Zhao, Ming-gao Zhuo, Min Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title | Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title_full | Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title_fullStr | Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title_full_unstemmed | Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title_short | Characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
title_sort | characterization of serotonin-induced inhibition of excitatory synaptic transmission in the anterior cingulate cortex |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5468981/ https://www.ncbi.nlm.nih.gov/pubmed/28606116 http://dx.doi.org/10.1186/s13041-017-0303-1 |
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