Cargando…

Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa

Jerboas are wild rodents exhibiting exceptional adaptation to their desert environment. Under harsh autumn conditions, they shut down reproduction, increase body weight and hibernate, while during spring they become sexually active even under negative energy-balance. We recently reported that these...

Descripción completa

Detalles Bibliográficos
Autores principales: Talbi, Rajae, Laran-Chich, Marie-Pierre, Magoul, Rabia, El Ouezzani, Seloua, Simonneaux, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090964/
https://www.ncbi.nlm.nih.gov/pubmed/27805048
http://dx.doi.org/10.1038/srep36057
_version_ 1782464492727173120
author Talbi, Rajae
Laran-Chich, Marie-Pierre
Magoul, Rabia
El Ouezzani, Seloua
Simonneaux, Valérie
author_facet Talbi, Rajae
Laran-Chich, Marie-Pierre
Magoul, Rabia
El Ouezzani, Seloua
Simonneaux, Valérie
author_sort Talbi, Rajae
collection PubMed
description Jerboas are wild rodents exhibiting exceptional adaptation to their desert environment. Under harsh autumn conditions, they shut down reproduction, increase body weight and hibernate, while during spring they become sexually active even under negative energy-balance. We recently reported that these rhythms are associated with synchronized changes in genes expressing reproductive (Kiss1, Rfrp) and metabolic (Npy and Pomc) peptides, raising the hypothesis of coordinated seasonal regulation of both functions. Here we analyzed whether kisspeptin and RFRP-3 regulate food-intake in parallel to their established reproductive functions. Intracerebroventricular administration of kisspeptin inhibited food intake by 1.5-fold in fasted, but not ad-libitum fed, female jerboas captured in spring, an effect associated with an increase in Pomc and decrease in Rfrp mRNA levels. By contrast, intracerebroventricular injection of RFRP-3 induced a 4-fold increase in food-intake in ad-libitum female jerboas, together with a decrease in Pomc and increase in Npy mRNA levels. This orexigenic effect of RFRP-3 was observed in both spring and autumn, whereas kisspeptin’s anorexigenic effect was only observed in spring. Altogether, this study reports opposite metabolic effects of kisspeptin and RFRP-3 in the female jerboa and strengthens our hypothesis of a coordinated, season-dependent, regulation of reproductive activity and food intake through interactions of these hypothalamic peptides.
format Online
Article
Text
id pubmed-5090964
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50909642016-11-08 Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa Talbi, Rajae Laran-Chich, Marie-Pierre Magoul, Rabia El Ouezzani, Seloua Simonneaux, Valérie Sci Rep Article Jerboas are wild rodents exhibiting exceptional adaptation to their desert environment. Under harsh autumn conditions, they shut down reproduction, increase body weight and hibernate, while during spring they become sexually active even under negative energy-balance. We recently reported that these rhythms are associated with synchronized changes in genes expressing reproductive (Kiss1, Rfrp) and metabolic (Npy and Pomc) peptides, raising the hypothesis of coordinated seasonal regulation of both functions. Here we analyzed whether kisspeptin and RFRP-3 regulate food-intake in parallel to their established reproductive functions. Intracerebroventricular administration of kisspeptin inhibited food intake by 1.5-fold in fasted, but not ad-libitum fed, female jerboas captured in spring, an effect associated with an increase in Pomc and decrease in Rfrp mRNA levels. By contrast, intracerebroventricular injection of RFRP-3 induced a 4-fold increase in food-intake in ad-libitum female jerboas, together with a decrease in Pomc and increase in Npy mRNA levels. This orexigenic effect of RFRP-3 was observed in both spring and autumn, whereas kisspeptin’s anorexigenic effect was only observed in spring. Altogether, this study reports opposite metabolic effects of kisspeptin and RFRP-3 in the female jerboa and strengthens our hypothesis of a coordinated, season-dependent, regulation of reproductive activity and food intake through interactions of these hypothalamic peptides. Nature Publishing Group 2016-11-02 /pmc/articles/PMC5090964/ /pubmed/27805048 http://dx.doi.org/10.1038/srep36057 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
Talbi, Rajae
Laran-Chich, Marie-Pierre
Magoul, Rabia
El Ouezzani, Seloua
Simonneaux, Valérie
Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title_full Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title_fullStr Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title_full_unstemmed Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title_short Kisspeptin and RFRP-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
title_sort kisspeptin and rfrp-3 differentially regulate food intake and metabolic neuropeptides in the female desert jerboa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090964/
https://www.ncbi.nlm.nih.gov/pubmed/27805048
http://dx.doi.org/10.1038/srep36057
work_keys_str_mv AT talbirajae kisspeptinandrfrp3differentiallyregulatefoodintakeandmetabolicneuropeptidesinthefemaledesertjerboa
AT laranchichmariepierre kisspeptinandrfrp3differentiallyregulatefoodintakeandmetabolicneuropeptidesinthefemaledesertjerboa
AT magoulrabia kisspeptinandrfrp3differentiallyregulatefoodintakeandmetabolicneuropeptidesinthefemaledesertjerboa
AT elouezzaniseloua kisspeptinandrfrp3differentiallyregulatefoodintakeandmetabolicneuropeptidesinthefemaledesertjerboa
AT simonneauxvalerie kisspeptinandrfrp3differentiallyregulatefoodintakeandmetabolicneuropeptidesinthefemaledesertjerboa