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Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system

The habenula, located on the dorsal thalamic surface, is an emotional and reward processing center. As in the mammalian brain, the zebrafish habenula is divided into dorsal (dHb) and ventral (vHb) subdivisions that project to the interpeduncular nucleus and median raphe (MR) respectively. Previously...

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Autores principales: Nathan, Fatima M., Ogawa, Satoshi, Parhar, Ishwar S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049628/
https://www.ncbi.nlm.nih.gov/pubmed/26250886
http://dx.doi.org/10.1111/jnc.13273
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author Nathan, Fatima M.
Ogawa, Satoshi
Parhar, Ishwar S.
author_facet Nathan, Fatima M.
Ogawa, Satoshi
Parhar, Ishwar S.
author_sort Nathan, Fatima M.
collection PubMed
description The habenula, located on the dorsal thalamic surface, is an emotional and reward processing center. As in the mammalian brain, the zebrafish habenula is divided into dorsal (dHb) and ventral (vHb) subdivisions that project to the interpeduncular nucleus and median raphe (MR) respectively. Previously, we have shown that kisspeptin 1 (Kiss1) expressing in the vHb, regulates the serotonin (5‐HT) system in the MR. However, the connectivity between the Kiss1 neurons and the 5‐HT system remains unknown. To resolve this issue, we generated a specific antibody against zebrafish Kiss1 receptor (Kiss‐R1); using this primary antibody we found intense immunohistochemical labeling in the ventro‐anterior corner of the MR (vaMR) but not in 5‐HT neurons, suggesting the potential involvement of interneurons in 5‐HT modulation by Kiss1. Double‐fluorescence labeling showed that the majority of habenular Kiss1 neurons are glutamatergic. In the MR region, Kiss1 fibers were mainly seen in close association with glutamatergic neurons and only scarcely within GABAergic and 5‐HT neurons. Our findings indicate that the habenular Kiss1 neurons potentially modulate the 5‐HT system primarily through glutamatergic neurotransmission via as yet uncharacterized interneurons. [Image: see text] The neuropeptide kisspeptin (Kiss1) play a key role in vertebrate reproduction. We have previously shown modulatory role of habenular Kiss1 in the raphe serotonin (5‐HT) systems. This study proposed that the habenular Kiss1 neurons modulate the 5‐HT system primarily through glutamatergic neurotransmission, which provides an important insight for understanding of the modulation of 5‐HT system by the habenula‐raphe pathway.
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spelling pubmed-50496282016-10-06 Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system Nathan, Fatima M. Ogawa, Satoshi Parhar, Ishwar S. J Neurochem ORIGINAL ARTICLES The habenula, located on the dorsal thalamic surface, is an emotional and reward processing center. As in the mammalian brain, the zebrafish habenula is divided into dorsal (dHb) and ventral (vHb) subdivisions that project to the interpeduncular nucleus and median raphe (MR) respectively. Previously, we have shown that kisspeptin 1 (Kiss1) expressing in the vHb, regulates the serotonin (5‐HT) system in the MR. However, the connectivity between the Kiss1 neurons and the 5‐HT system remains unknown. To resolve this issue, we generated a specific antibody against zebrafish Kiss1 receptor (Kiss‐R1); using this primary antibody we found intense immunohistochemical labeling in the ventro‐anterior corner of the MR (vaMR) but not in 5‐HT neurons, suggesting the potential involvement of interneurons in 5‐HT modulation by Kiss1. Double‐fluorescence labeling showed that the majority of habenular Kiss1 neurons are glutamatergic. In the MR region, Kiss1 fibers were mainly seen in close association with glutamatergic neurons and only scarcely within GABAergic and 5‐HT neurons. Our findings indicate that the habenular Kiss1 neurons potentially modulate the 5‐HT system primarily through glutamatergic neurotransmission via as yet uncharacterized interneurons. [Image: see text] The neuropeptide kisspeptin (Kiss1) play a key role in vertebrate reproduction. We have previously shown modulatory role of habenular Kiss1 in the raphe serotonin (5‐HT) systems. This study proposed that the habenular Kiss1 neurons modulate the 5‐HT system primarily through glutamatergic neurotransmission, which provides an important insight for understanding of the modulation of 5‐HT system by the habenula‐raphe pathway. John Wiley and Sons Inc. 2015-09-10 2015-11 /pmc/articles/PMC5049628/ /pubmed/26250886 http://dx.doi.org/10.1111/jnc.13273 Text en © 2015 Monash University Malaysia. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (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 ORIGINAL ARTICLES
Nathan, Fatima M.
Ogawa, Satoshi
Parhar, Ishwar S.
Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title_full Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title_fullStr Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title_full_unstemmed Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title_short Neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐HT system
title_sort neuronal connectivity between habenular glutamate‐kisspeptin1 co‐expressing neurons and the raphe 5‐ht system
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5049628/
https://www.ncbi.nlm.nih.gov/pubmed/26250886
http://dx.doi.org/10.1111/jnc.13273
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