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Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula
The medial habenula (MHb) plays an important role in nicotine-related behaviors such as nicotine aversion and withdrawal. The MHb receives GABAergic input from the medial septum/diagonal band of Broca (MS/DB), yet the synaptic mechanism that regulates MHb activity is unclear. GABA (γ -aminobutyric a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050514/ https://www.ncbi.nlm.nih.gov/pubmed/27703268 http://dx.doi.org/10.1038/srep34800 |
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author | Choi, Kyuhyun Lee, Youngin Lee, Changwoo Hong, Seokheon Lee, Soonje Kang, Shin Jung Shin, Ki Soon |
author_facet | Choi, Kyuhyun Lee, Youngin Lee, Changwoo Hong, Seokheon Lee, Soonje Kang, Shin Jung Shin, Ki Soon |
author_sort | Choi, Kyuhyun |
collection | PubMed |
description | The medial habenula (MHb) plays an important role in nicotine-related behaviors such as nicotine aversion and withdrawal. The MHb receives GABAergic input from the medial septum/diagonal band of Broca (MS/DB), yet the synaptic mechanism that regulates MHb activity is unclear. GABA (γ -aminobutyric acid) is a major inhibitory neurotransmitter activating both GABA(A) receptors and GABA(B) receptors. Depending on intracellular chloride concentration, however, GABA(A) receptors also function in an excitatory manner. In the absence of various synaptic inputs, we found that MHb neurons displayed spontaneous tonic firing at a rate of about ~4.4 Hz. Optogenetic stimulation of MS/DB inputs to the MHb evoked GABA(A) receptor-mediated synaptic currents, which produced stimulus-locked neuronal firing. Subsequent delayed yet lasting activation of GABA(B) receptors attenuated the intrinsic tonic firing. Consequently, septal GABAergic input alone orchestrates both excitatory GABA(A) and inhibitory GABA(B) receptors, thereby entraining the firing of MHb neurons. |
format | Online Article Text |
id | pubmed-5050514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50505142016-10-11 Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula Choi, Kyuhyun Lee, Youngin Lee, Changwoo Hong, Seokheon Lee, Soonje Kang, Shin Jung Shin, Ki Soon Sci Rep Article The medial habenula (MHb) plays an important role in nicotine-related behaviors such as nicotine aversion and withdrawal. The MHb receives GABAergic input from the medial septum/diagonal band of Broca (MS/DB), yet the synaptic mechanism that regulates MHb activity is unclear. GABA (γ -aminobutyric acid) is a major inhibitory neurotransmitter activating both GABA(A) receptors and GABA(B) receptors. Depending on intracellular chloride concentration, however, GABA(A) receptors also function in an excitatory manner. In the absence of various synaptic inputs, we found that MHb neurons displayed spontaneous tonic firing at a rate of about ~4.4 Hz. Optogenetic stimulation of MS/DB inputs to the MHb evoked GABA(A) receptor-mediated synaptic currents, which produced stimulus-locked neuronal firing. Subsequent delayed yet lasting activation of GABA(B) receptors attenuated the intrinsic tonic firing. Consequently, septal GABAergic input alone orchestrates both excitatory GABA(A) and inhibitory GABA(B) receptors, thereby entraining the firing of MHb neurons. Nature Publishing Group 2016-10-05 /pmc/articles/PMC5050514/ /pubmed/27703268 http://dx.doi.org/10.1038/srep34800 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Choi, Kyuhyun Lee, Youngin Lee, Changwoo Hong, Seokheon Lee, Soonje Kang, Shin Jung Shin, Ki Soon Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title | Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title_full | Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title_fullStr | Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title_full_unstemmed | Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title_short | Optogenetic activation of septal GABAergic afferents entrains neuronal firing in the medial habenula |
title_sort | optogenetic activation of septal gabaergic afferents entrains neuronal firing in the medial habenula |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5050514/ https://www.ncbi.nlm.nih.gov/pubmed/27703268 http://dx.doi.org/10.1038/srep34800 |
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