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CC002/Unc females are mouse models of exercise‐induced paradoxical fat response
Exercise results in beneficial health outcomes and protects against a variety of chronic diseases. However, U.S. exercise guidelines recommend identical exercise programs for everyone, despite individual variation in responses to these programs, including paradoxical fat gain. Experimental models of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009762/ https://www.ncbi.nlm.nih.gov/pubmed/29924460 http://dx.doi.org/10.14814/phy2.13716 |
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author | McMullan, Rachel C. Ferris, Martin T. Bell, Timothy A. Menachery, Vineet D. Baric, Ralph S. Hua, Kunjie Pomp, Daniel Smith‐Ryan, Abbie E. de Villena, Fernando Pardo‐Manuel |
author_facet | McMullan, Rachel C. Ferris, Martin T. Bell, Timothy A. Menachery, Vineet D. Baric, Ralph S. Hua, Kunjie Pomp, Daniel Smith‐Ryan, Abbie E. de Villena, Fernando Pardo‐Manuel |
author_sort | McMullan, Rachel C. |
collection | PubMed |
description | Exercise results in beneficial health outcomes and protects against a variety of chronic diseases. However, U.S. exercise guidelines recommend identical exercise programs for everyone, despite individual variation in responses to these programs, including paradoxical fat gain. Experimental models of exercise‐induced paradoxical outcomes may enable the dissection of underlying physiological mechanisms as well as the evaluation of potential interventions. Whereas several studies have identified individual mice exhibiting paradoxical fat gain following exercise, no systematic effort has been conducted to identify and characterize models of paradoxical response. Strains from the Collaborative Cross (CC) genetic reference population were used due to its high levels of genetic variation, its reproducible nature, and the observation that the CC is a rich source of novel disease models, to assess the impact genetic background has on exercise responses. We identified the strain CC002/Unc as an exercise‐induced paradoxical fat response model in a controlled voluntary exercise study across multiple ages in female mice. We also found sex and genetic differences were consistent with this pattern in a study of forced exercise programs. These results provide a novel model for studies to determine the mechanisms behind paradoxical metabolic responses to exercise, and enable development of more rational personalized exercise recommendations based on factors such as age, sex, and genetic background. |
format | Online Article Text |
id | pubmed-6009762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60097622018-06-21 CC002/Unc females are mouse models of exercise‐induced paradoxical fat response McMullan, Rachel C. Ferris, Martin T. Bell, Timothy A. Menachery, Vineet D. Baric, Ralph S. Hua, Kunjie Pomp, Daniel Smith‐Ryan, Abbie E. de Villena, Fernando Pardo‐Manuel Physiol Rep Original Research Exercise results in beneficial health outcomes and protects against a variety of chronic diseases. However, U.S. exercise guidelines recommend identical exercise programs for everyone, despite individual variation in responses to these programs, including paradoxical fat gain. Experimental models of exercise‐induced paradoxical outcomes may enable the dissection of underlying physiological mechanisms as well as the evaluation of potential interventions. Whereas several studies have identified individual mice exhibiting paradoxical fat gain following exercise, no systematic effort has been conducted to identify and characterize models of paradoxical response. Strains from the Collaborative Cross (CC) genetic reference population were used due to its high levels of genetic variation, its reproducible nature, and the observation that the CC is a rich source of novel disease models, to assess the impact genetic background has on exercise responses. We identified the strain CC002/Unc as an exercise‐induced paradoxical fat response model in a controlled voluntary exercise study across multiple ages in female mice. We also found sex and genetic differences were consistent with this pattern in a study of forced exercise programs. These results provide a novel model for studies to determine the mechanisms behind paradoxical metabolic responses to exercise, and enable development of more rational personalized exercise recommendations based on factors such as age, sex, and genetic background. John Wiley and Sons Inc. 2018-06-19 /pmc/articles/PMC6009762/ /pubmed/29924460 http://dx.doi.org/10.14814/phy2.13716 Text en © 2018 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research McMullan, Rachel C. Ferris, Martin T. Bell, Timothy A. Menachery, Vineet D. Baric, Ralph S. Hua, Kunjie Pomp, Daniel Smith‐Ryan, Abbie E. de Villena, Fernando Pardo‐Manuel CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title |
CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title_full |
CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title_fullStr |
CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title_full_unstemmed |
CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title_short |
CC002/Unc females are mouse models of exercise‐induced paradoxical fat response |
title_sort | cc002/unc females are mouse models of exercise‐induced paradoxical fat response |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009762/ https://www.ncbi.nlm.nih.gov/pubmed/29924460 http://dx.doi.org/10.14814/phy2.13716 |
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