Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Abdul Satar, Nurul M., Ogawa, Satoshi, Parhar, Ishwar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783607789429456896
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
work_keys_str_mv AT abdulsatarnurulm kisspeptin1regulatesforebraindopaminergicneuronsinthezebrafish
AT ogawasatoshi kisspeptin1regulatesforebraindopaminergicneuronsinthezebrafish
AT parharishwars kisspeptin1regulatesforebraindopaminergicneuronsinthezebrafish