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Identification of GABAergic neurons innervating the zebrafish lateral habenula
Habenula neurons are constantly active. The level of activity affects mood and behaviour, with increased activity in the lateral habenula reflecting exposure to punishment and a switch to passive coping and depression. Here, we identify GABAergic neurons that could reduce activity in the lateral hab...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689879/ https://www.ncbi.nlm.nih.gov/pubmed/32464693 http://dx.doi.org/10.1111/ejn.14843 |
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author | Ramaswamy, Mahathi Cheng, Ruey‐Kuang Jesuthasan, Suresh |
author_facet | Ramaswamy, Mahathi Cheng, Ruey‐Kuang Jesuthasan, Suresh |
author_sort | Ramaswamy, Mahathi |
collection | PubMed |
description | Habenula neurons are constantly active. The level of activity affects mood and behaviour, with increased activity in the lateral habenula reflecting exposure to punishment and a switch to passive coping and depression. Here, we identify GABAergic neurons that could reduce activity in the lateral habenula of larval zebrafish. GAD65/67 immunohistochemistry and imaging of gad1b:DsRed transgenic fish suggest the presence of GABAergic terminals in the neuropil and between cell bodies in the lateral habenula. Retrograde tracing with the lipophilic dye DiD suggests that the former derives from the thalamus, while the latter originates from a group of cells in the posterior hypothalamus that are located between the posterior tuberal nucleus and hypothalamic lobes. Two‐photon calcium imaging indicates that blue light causes excitation of thalamic GABAergic neurons and terminals in the neuropil, while a subpopulation of lateral habenula neurons show reduced intracellular calcium levels. Whole‐cell electrophysiological recording indicates that blue light reduces membrane potential of lateral habenula neurons. These observations suggest that GABAergic input from the thalamus may mediate inhibition in the zebrafish lateral habenula. Mechanisms governing release of GABA from the neurons in the posterior hypothalamus, which are likely to be in the tuberomammillary nucleus, remain to be defined. |
format | Online Article Text |
id | pubmed-7689879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76898792020-12-08 Identification of GABAergic neurons innervating the zebrafish lateral habenula Ramaswamy, Mahathi Cheng, Ruey‐Kuang Jesuthasan, Suresh Eur J Neurosci Systems Neuroscience Habenula neurons are constantly active. The level of activity affects mood and behaviour, with increased activity in the lateral habenula reflecting exposure to punishment and a switch to passive coping and depression. Here, we identify GABAergic neurons that could reduce activity in the lateral habenula of larval zebrafish. GAD65/67 immunohistochemistry and imaging of gad1b:DsRed transgenic fish suggest the presence of GABAergic terminals in the neuropil and between cell bodies in the lateral habenula. Retrograde tracing with the lipophilic dye DiD suggests that the former derives from the thalamus, while the latter originates from a group of cells in the posterior hypothalamus that are located between the posterior tuberal nucleus and hypothalamic lobes. Two‐photon calcium imaging indicates that blue light causes excitation of thalamic GABAergic neurons and terminals in the neuropil, while a subpopulation of lateral habenula neurons show reduced intracellular calcium levels. Whole‐cell electrophysiological recording indicates that blue light reduces membrane potential of lateral habenula neurons. These observations suggest that GABAergic input from the thalamus may mediate inhibition in the zebrafish lateral habenula. Mechanisms governing release of GABA from the neurons in the posterior hypothalamus, which are likely to be in the tuberomammillary nucleus, remain to be defined. John Wiley and Sons Inc. 2020-06-30 2020-10 /pmc/articles/PMC7689879/ /pubmed/32464693 http://dx.doi.org/10.1111/ejn.14843 Text en © 2020 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Systems Neuroscience Ramaswamy, Mahathi Cheng, Ruey‐Kuang Jesuthasan, Suresh Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title | Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title_full | Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title_fullStr | Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title_full_unstemmed | Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title_short | Identification of GABAergic neurons innervating the zebrafish lateral habenula |
title_sort | identification of gabaergic neurons innervating the zebrafish lateral habenula |
topic | Systems Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689879/ https://www.ncbi.nlm.nih.gov/pubmed/32464693 http://dx.doi.org/10.1111/ejn.14843 |
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