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Maternal predator odour exposure programs metabolic responses in adult offspring
A cardinal feature of the reaction to stress is the promotion of energy mobilization, enabling appropriate behavioural responses. Predator odours are naturalistic and ecologically relevant stressors present over evolutionary timescales. In this study, we asked whether maternal predator odour exposur...
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/PMC5967341/ https://www.ncbi.nlm.nih.gov/pubmed/29799024 http://dx.doi.org/10.1038/s41598-018-26462-w |
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author | St-Cyr, Sophie Abuaish, Sameera Welch, Kenneth C. McGowan, Patrick O. |
author_facet | St-Cyr, Sophie Abuaish, Sameera Welch, Kenneth C. McGowan, Patrick O. |
author_sort | St-Cyr, Sophie |
collection | PubMed |
description | A cardinal feature of the reaction to stress is the promotion of energy mobilization, enabling appropriate behavioural responses. Predator odours are naturalistic and ecologically relevant stressors present over evolutionary timescales. In this study, we asked whether maternal predator odour exposure could program long-term energy mobilization in C57BL/6 mice offspring. To test this hypothesis, we measured rates of oxygen consumption in prenatally predator odour exposed mice in adulthood while controlling for levels of locomotor activity at baseline and under stress. Circulating thyroid hormone levels and the transcript abundance of key regulators of the hypothalamic-pituitary-thyroid axis within the periventricular nucleus (PVN) of the hypothalamus and in the liver, including carriers and receptors and thyrotropin-releasing hormone, were measured as endocrine mediators facilitating energy availability. Prenatally predator odour exposed mice of both sexes mobilized more energy during lower energy demand periods of the day and under stressful conditions. Further, prenatally predator odour exposed mice displayed modifications of their hypothalamic-pituitary-thyroid axis through increased circulating thyroxine and thyroid hormone receptor α within the PVN and decreased transthyretin in the liver. Overall, these results suggest that maternal exposure to predator odour is sufficient to increase long-term energy mobilization in adult offspring. |
format | Online Article Text |
id | pubmed-5967341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59673412018-05-30 Maternal predator odour exposure programs metabolic responses in adult offspring St-Cyr, Sophie Abuaish, Sameera Welch, Kenneth C. McGowan, Patrick O. Sci Rep Article A cardinal feature of the reaction to stress is the promotion of energy mobilization, enabling appropriate behavioural responses. Predator odours are naturalistic and ecologically relevant stressors present over evolutionary timescales. In this study, we asked whether maternal predator odour exposure could program long-term energy mobilization in C57BL/6 mice offspring. To test this hypothesis, we measured rates of oxygen consumption in prenatally predator odour exposed mice in adulthood while controlling for levels of locomotor activity at baseline and under stress. Circulating thyroid hormone levels and the transcript abundance of key regulators of the hypothalamic-pituitary-thyroid axis within the periventricular nucleus (PVN) of the hypothalamus and in the liver, including carriers and receptors and thyrotropin-releasing hormone, were measured as endocrine mediators facilitating energy availability. Prenatally predator odour exposed mice of both sexes mobilized more energy during lower energy demand periods of the day and under stressful conditions. Further, prenatally predator odour exposed mice displayed modifications of their hypothalamic-pituitary-thyroid axis through increased circulating thyroxine and thyroid hormone receptor α within the PVN and decreased transthyretin in the liver. Overall, these results suggest that maternal exposure to predator odour is sufficient to increase long-term energy mobilization in adult offspring. Nature Publishing Group UK 2018-05-24 /pmc/articles/PMC5967341/ /pubmed/29799024 http://dx.doi.org/10.1038/s41598-018-26462-w 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 St-Cyr, Sophie Abuaish, Sameera Welch, Kenneth C. McGowan, Patrick O. Maternal predator odour exposure programs metabolic responses in adult offspring |
title | Maternal predator odour exposure programs metabolic responses in adult offspring |
title_full | Maternal predator odour exposure programs metabolic responses in adult offspring |
title_fullStr | Maternal predator odour exposure programs metabolic responses in adult offspring |
title_full_unstemmed | Maternal predator odour exposure programs metabolic responses in adult offspring |
title_short | Maternal predator odour exposure programs metabolic responses in adult offspring |
title_sort | maternal predator odour exposure programs metabolic responses in adult offspring |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967341/ https://www.ncbi.nlm.nih.gov/pubmed/29799024 http://dx.doi.org/10.1038/s41598-018-26462-w |
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