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Adult male mice exposure to nonylphenol alters courtship vocalizations and mating
The neural circuitry processing male sexual behavior is tightly regulated by testosterone and its neural metabolite estradiol. The present study evaluated the effects of adult exposure to low doses of nonylphenol (NP), a widespread environmental contaminant, on the neuroendocrine regulation of testo...
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/PMC5813014/ https://www.ncbi.nlm.nih.gov/pubmed/29445187 http://dx.doi.org/10.1038/s41598-018-21245-9 |
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author | Capela, Daphné Dombret, Carlos Poissenot, Kevin Poignant, Manon Malbert-Colas, Aude Franceschini, Isabelle Keller, Matthieu Mhaouty-Kodja, Sakina |
author_facet | Capela, Daphné Dombret, Carlos Poissenot, Kevin Poignant, Manon Malbert-Colas, Aude Franceschini, Isabelle Keller, Matthieu Mhaouty-Kodja, Sakina |
author_sort | Capela, Daphné |
collection | PubMed |
description | The neural circuitry processing male sexual behavior is tightly regulated by testosterone and its neural metabolite estradiol. The present study evaluated the effects of adult exposure to low doses of nonylphenol (NP), a widespread environmental contaminant, on the neuroendocrine regulation of testosterone and expression of sexual behavior. Oral exposure of C57BL/6J males to NP (0.5, 5 or 50 μg/kg/day) for 4 weeks did not affect circulating levels of testosterone or the kisspeptin system, a key regulator of the gonadotropic axis. In contrast, mice exposed to NP at 5 μg/kg/day emitted an increased number and duration of ultrasonic vocalizations, took longer to reach ejaculation and showed increased number of mounts, intromissions and thrusts. This was associated with normal olfactory preference and locomotor activity, and increased anxiety level. Analysis of the neural circuitry that underlies sexual behavior showed changes in the number of cells expressing androgen and estrogen receptors in males exposed to NP at 5 μg/kg/day. The neural circuitry underlying sexual behavior is thus highly sensitive to adult exposure to NP. Furthermore, almost all the observed effects were induced at 5 μg/kg/day of NP, indicating that this endocrine disrupter triggers a non-monotonic response in the adult male mouse brain. |
format | Online Article Text |
id | pubmed-5813014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58130142018-02-21 Adult male mice exposure to nonylphenol alters courtship vocalizations and mating Capela, Daphné Dombret, Carlos Poissenot, Kevin Poignant, Manon Malbert-Colas, Aude Franceschini, Isabelle Keller, Matthieu Mhaouty-Kodja, Sakina Sci Rep Article The neural circuitry processing male sexual behavior is tightly regulated by testosterone and its neural metabolite estradiol. The present study evaluated the effects of adult exposure to low doses of nonylphenol (NP), a widespread environmental contaminant, on the neuroendocrine regulation of testosterone and expression of sexual behavior. Oral exposure of C57BL/6J males to NP (0.5, 5 or 50 μg/kg/day) for 4 weeks did not affect circulating levels of testosterone or the kisspeptin system, a key regulator of the gonadotropic axis. In contrast, mice exposed to NP at 5 μg/kg/day emitted an increased number and duration of ultrasonic vocalizations, took longer to reach ejaculation and showed increased number of mounts, intromissions and thrusts. This was associated with normal olfactory preference and locomotor activity, and increased anxiety level. Analysis of the neural circuitry that underlies sexual behavior showed changes in the number of cells expressing androgen and estrogen receptors in males exposed to NP at 5 μg/kg/day. The neural circuitry underlying sexual behavior is thus highly sensitive to adult exposure to NP. Furthermore, almost all the observed effects were induced at 5 μg/kg/day of NP, indicating that this endocrine disrupter triggers a non-monotonic response in the adult male mouse brain. Nature Publishing Group UK 2018-02-14 /pmc/articles/PMC5813014/ /pubmed/29445187 http://dx.doi.org/10.1038/s41598-018-21245-9 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 Capela, Daphné Dombret, Carlos Poissenot, Kevin Poignant, Manon Malbert-Colas, Aude Franceschini, Isabelle Keller, Matthieu Mhaouty-Kodja, Sakina Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title | Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title_full | Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title_fullStr | Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title_full_unstemmed | Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title_short | Adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
title_sort | adult male mice exposure to nonylphenol alters courtship vocalizations and mating |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813014/ https://www.ncbi.nlm.nih.gov/pubmed/29445187 http://dx.doi.org/10.1038/s41598-018-21245-9 |
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