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Female sexual behavior in mice is controlled by kisspeptin neurons
Sexual behavior is essential for the survival of many species. In female rodents, mate preference and copulatory behavior depend on pheromones and are synchronized with ovulation to ensure reproductive success. The neural circuits driving this orchestration in the brain have, however, remained elusi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786055/ https://www.ncbi.nlm.nih.gov/pubmed/29374161 http://dx.doi.org/10.1038/s41467-017-02797-2 |
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author | Hellier, Vincent Brock, Olivier Candlish, Michael Desroziers, Elodie Aoki, Mari Mayer, Christian Piet, Richard Herbison, Allan Colledge, William Henry Prévot, Vincent Boehm, Ulrich Bakker, Julie |
author_facet | Hellier, Vincent Brock, Olivier Candlish, Michael Desroziers, Elodie Aoki, Mari Mayer, Christian Piet, Richard Herbison, Allan Colledge, William Henry Prévot, Vincent Boehm, Ulrich Bakker, Julie |
author_sort | Hellier, Vincent |
collection | PubMed |
description | Sexual behavior is essential for the survival of many species. In female rodents, mate preference and copulatory behavior depend on pheromones and are synchronized with ovulation to ensure reproductive success. The neural circuits driving this orchestration in the brain have, however, remained elusive. Here, we demonstrate that neurons controlling ovulation in the mammalian brain are at the core of a branching neural circuit governing both mate preference and copulatory behavior. We show that male odors detected in the vomeronasal organ activate kisspeptin neurons in female mice. Classical kisspeptin/Kiss1R signaling subsequently triggers olfactory-driven mate preference. In contrast, copulatory behavior is elicited by kisspeptin neurons in a parallel circuit independent of Kiss1R involving nitric oxide signaling. Consistent with this, we find that kisspeptin neurons impinge onto nitric oxide-synthesizing neurons in the ventromedial hypothalamus. Our data establish kisspeptin neurons as a central regulatory hub orchestrating sexual behavior in the female mouse brain. |
format | Online Article Text |
id | pubmed-5786055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57860552018-01-29 Female sexual behavior in mice is controlled by kisspeptin neurons Hellier, Vincent Brock, Olivier Candlish, Michael Desroziers, Elodie Aoki, Mari Mayer, Christian Piet, Richard Herbison, Allan Colledge, William Henry Prévot, Vincent Boehm, Ulrich Bakker, Julie Nat Commun Article Sexual behavior is essential for the survival of many species. In female rodents, mate preference and copulatory behavior depend on pheromones and are synchronized with ovulation to ensure reproductive success. The neural circuits driving this orchestration in the brain have, however, remained elusive. Here, we demonstrate that neurons controlling ovulation in the mammalian brain are at the core of a branching neural circuit governing both mate preference and copulatory behavior. We show that male odors detected in the vomeronasal organ activate kisspeptin neurons in female mice. Classical kisspeptin/Kiss1R signaling subsequently triggers olfactory-driven mate preference. In contrast, copulatory behavior is elicited by kisspeptin neurons in a parallel circuit independent of Kiss1R involving nitric oxide signaling. Consistent with this, we find that kisspeptin neurons impinge onto nitric oxide-synthesizing neurons in the ventromedial hypothalamus. Our data establish kisspeptin neurons as a central regulatory hub orchestrating sexual behavior in the female mouse brain. Nature Publishing Group UK 2018-01-26 /pmc/articles/PMC5786055/ /pubmed/29374161 http://dx.doi.org/10.1038/s41467-017-02797-2 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hellier, Vincent Brock, Olivier Candlish, Michael Desroziers, Elodie Aoki, Mari Mayer, Christian Piet, Richard Herbison, Allan Colledge, William Henry Prévot, Vincent Boehm, Ulrich Bakker, Julie Female sexual behavior in mice is controlled by kisspeptin neurons |
title | Female sexual behavior in mice is controlled by kisspeptin neurons |
title_full | Female sexual behavior in mice is controlled by kisspeptin neurons |
title_fullStr | Female sexual behavior in mice is controlled by kisspeptin neurons |
title_full_unstemmed | Female sexual behavior in mice is controlled by kisspeptin neurons |
title_short | Female sexual behavior in mice is controlled by kisspeptin neurons |
title_sort | female sexual behavior in mice is controlled by kisspeptin neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786055/ https://www.ncbi.nlm.nih.gov/pubmed/29374161 http://dx.doi.org/10.1038/s41467-017-02797-2 |
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