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Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice

Metabolic functions are synchronized by the circadian clock setting daily patterns of food intake, nutrient delivery, and behavioral activity. Here, we study the impact of chronic jet‐lag (CJL) on metabolism, and test manipulations aimed to overcome potential alterations. We recorded weight gain in...

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Autores principales: Casiraghi, Leandro P., Alzamendi, Ana, Giovambattista, Andrés, Chiesa, Juan J., Golombek, Diego A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848717/
https://www.ncbi.nlm.nih.gov/pubmed/27125665
http://dx.doi.org/10.14814/phy2.12743
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author Casiraghi, Leandro P.
Alzamendi, Ana
Giovambattista, Andrés
Chiesa, Juan J.
Golombek, Diego A.
author_facet Casiraghi, Leandro P.
Alzamendi, Ana
Giovambattista, Andrés
Chiesa, Juan J.
Golombek, Diego A.
author_sort Casiraghi, Leandro P.
collection PubMed
description Metabolic functions are synchronized by the circadian clock setting daily patterns of food intake, nutrient delivery, and behavioral activity. Here, we study the impact of chronic jet‐lag (CJL) on metabolism, and test manipulations aimed to overcome potential alterations. We recorded weight gain in C57Bl/6 mice under chronic 6 h advances or delays of the light–dark cycle every 2 days (ChrA and ChrD, respectively). We have previously reported ChrA, but not ChrD, to induce forced desynchronization of locomotor activity rhythms in mice (Casiraghi et al. 2012). Body weight was rapidly increased under ChrA, with animals tripling the mean weight gain observed in controls by day 10, and doubling it by day 30 (6% vs. 2%, and 15% vs. 7%, respectively). Significant increases in retroperitoneal and epidydimal adipose tissue masses (172% and 61%, respectively), adipocytes size (28%), and circulating triglycerides (39%) were also detected. Daily patterns of food and water intake were abolished under ChrA. In contrast, ChrD had no effect on body weight. Wheel‐running, housing of animals in groups, and restriction of food availability to hours of darkness prevented abnormal increase in body weight under ChrA. Our findings suggest that the observed alterations under ChrA may arise either from a direct effect of circadian disruption on metabolism, from desynchronization between feeding and metabolic rhythms, or both. Direction of shifts, timing of feeding episodes, and other reinforcing signals deeply affect the outcome of metabolic function under CJL. Such features should be taken into account in further studies of shift working schedules in humans.
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spelling pubmed-48487172016-05-04 Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice Casiraghi, Leandro P. Alzamendi, Ana Giovambattista, Andrés Chiesa, Juan J. Golombek, Diego A. Physiol Rep Original Research Metabolic functions are synchronized by the circadian clock setting daily patterns of food intake, nutrient delivery, and behavioral activity. Here, we study the impact of chronic jet‐lag (CJL) on metabolism, and test manipulations aimed to overcome potential alterations. We recorded weight gain in C57Bl/6 mice under chronic 6 h advances or delays of the light–dark cycle every 2 days (ChrA and ChrD, respectively). We have previously reported ChrA, but not ChrD, to induce forced desynchronization of locomotor activity rhythms in mice (Casiraghi et al. 2012). Body weight was rapidly increased under ChrA, with animals tripling the mean weight gain observed in controls by day 10, and doubling it by day 30 (6% vs. 2%, and 15% vs. 7%, respectively). Significant increases in retroperitoneal and epidydimal adipose tissue masses (172% and 61%, respectively), adipocytes size (28%), and circulating triglycerides (39%) were also detected. Daily patterns of food and water intake were abolished under ChrA. In contrast, ChrD had no effect on body weight. Wheel‐running, housing of animals in groups, and restriction of food availability to hours of darkness prevented abnormal increase in body weight under ChrA. Our findings suggest that the observed alterations under ChrA may arise either from a direct effect of circadian disruption on metabolism, from desynchronization between feeding and metabolic rhythms, or both. Direction of shifts, timing of feeding episodes, and other reinforcing signals deeply affect the outcome of metabolic function under CJL. Such features should be taken into account in further studies of shift working schedules in humans. John Wiley and Sons Inc. 2016-04-28 /pmc/articles/PMC4848717/ /pubmed/27125665 http://dx.doi.org/10.14814/phy2.12743 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (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
Casiraghi, Leandro P.
Alzamendi, Ana
Giovambattista, Andrés
Chiesa, Juan J.
Golombek, Diego A.
Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title_full Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title_fullStr Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title_full_unstemmed Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title_short Effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
title_sort effects of chronic forced circadian desynchronization on body weight and metabolism in male mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848717/
https://www.ncbi.nlm.nih.gov/pubmed/27125665
http://dx.doi.org/10.14814/phy2.12743
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