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Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish
The habenula is a phylogenetically conserved epithalamic structure, which conveys negative information via inhibition of mesolimbic dopamine neurons. We have previously shown the expression of kisspeptin (Kiss1) in the habenula and its role in the modulation of fear responses in the zebrafish. In th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652893/ https://www.ncbi.nlm.nih.gov/pubmed/33168887 http://dx.doi.org/10.1038/s41598-020-75777-0 |
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author | Abdul Satar, Nurul M. Ogawa, Satoshi Parhar, Ishwar S. |
author_facet | Abdul Satar, Nurul M. Ogawa, Satoshi Parhar, Ishwar S. |
author_sort | Abdul Satar, Nurul M. |
collection | PubMed |
description | The habenula is a phylogenetically conserved epithalamic structure, which conveys negative information via inhibition of mesolimbic dopamine neurons. We have previously shown the expression of kisspeptin (Kiss1) in the habenula and its role in the modulation of fear responses in the zebrafish. In this study, to investigate whether habenular Kiss1 regulates fear responses via dopamine neurons in the zebrafish, Kiss1 peptides were intracranially administered close to the habenula, and the expression of dopamine-related genes (th1, th2 and dat) were examined in the brain using real-time PCR and dopamine levels using LC–MS/MS. th1 mRNA levels and dopamine levels were significantly increased in the telencephalon 24-h and 30-min after Kiss1 administration, respectively. In fish administered with Kiss1, expression of neural activity marker gene, npas4a and kiss1 gene were significantly decreased in the ventral habenula. Application of neural tracer into the median raphe, site of habenular Kiss1 neural terminal projections showed tracer-labelled projections in the medial forebrain bundle towards the telencephalon where dopamine neurons reside. These results suggest that Kiss1 negatively regulates its own neuronal activity in the ventral habenula via autocrine action. This, in turn affects neurons of the median raphe via interneurons, which project to the telencephalic dopaminergic neurons. |
format | Online Article Text |
id | pubmed-7652893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76528932020-11-12 Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish Abdul Satar, Nurul M. Ogawa, Satoshi Parhar, Ishwar S. Sci Rep Article The habenula is a phylogenetically conserved epithalamic structure, which conveys negative information via inhibition of mesolimbic dopamine neurons. We have previously shown the expression of kisspeptin (Kiss1) in the habenula and its role in the modulation of fear responses in the zebrafish. In this study, to investigate whether habenular Kiss1 regulates fear responses via dopamine neurons in the zebrafish, Kiss1 peptides were intracranially administered close to the habenula, and the expression of dopamine-related genes (th1, th2 and dat) were examined in the brain using real-time PCR and dopamine levels using LC–MS/MS. th1 mRNA levels and dopamine levels were significantly increased in the telencephalon 24-h and 30-min after Kiss1 administration, respectively. In fish administered with Kiss1, expression of neural activity marker gene, npas4a and kiss1 gene were significantly decreased in the ventral habenula. Application of neural tracer into the median raphe, site of habenular Kiss1 neural terminal projections showed tracer-labelled projections in the medial forebrain bundle towards the telencephalon where dopamine neurons reside. These results suggest that Kiss1 negatively regulates its own neuronal activity in the ventral habenula via autocrine action. This, in turn affects neurons of the median raphe via interneurons, which project to the telencephalic dopaminergic neurons. Nature Publishing Group UK 2020-11-09 /pmc/articles/PMC7652893/ /pubmed/33168887 http://dx.doi.org/10.1038/s41598-020-75777-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Abdul Satar, Nurul M. Ogawa, Satoshi Parhar, Ishwar S. Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title | Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title_full | Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title_fullStr | Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title_full_unstemmed | Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title_short | Kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
title_sort | kisspeptin-1 regulates forebrain dopaminergic neurons in the zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652893/ https://www.ncbi.nlm.nih.gov/pubmed/33168887 http://dx.doi.org/10.1038/s41598-020-75777-0 |
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