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Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold
BACKGROUND: Daily cyclic changes in environmental conditions are key signals for anticipatory and adaptive adjustments of most living species, including mammals. Lower ambient temperature stimulates the thermogenic activity of brown adipose tissue (BAT) and skeletal muscle. Given that the molecular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932155/ https://www.ncbi.nlm.nih.gov/pubmed/29755411 http://dx.doi.org/10.3389/fendo.2018.00199 |
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author | Machado, Frederico Sander Mansur Zhang, Zhi Su, Yan de Goede, Paul Jansen, Remi Foppen, Ewout Coimbra, Cândido Celso Kalsbeek, Andries |
author_facet | Machado, Frederico Sander Mansur Zhang, Zhi Su, Yan de Goede, Paul Jansen, Remi Foppen, Ewout Coimbra, Cândido Celso Kalsbeek, Andries |
author_sort | Machado, Frederico Sander Mansur |
collection | PubMed |
description | BACKGROUND: Daily cyclic changes in environmental conditions are key signals for anticipatory and adaptive adjustments of most living species, including mammals. Lower ambient temperature stimulates the thermogenic activity of brown adipose tissue (BAT) and skeletal muscle. Given that the molecular components of the endogenous biological clock interact with thermal and metabolic mechanisms directly involved in the defense of body temperature, the present study evaluated the differential homeostatic responses to a cold stimulus at distinct time-windows of the light/dark-cycle. METHODS: Male Wistar rats were subjected to a single episode of 3 h cold ambient temperature (4°C) at one of 6 time-points starting at Zeitgeber Times 3, 7, 11, 15, 19, and 23. Metabolic rate, core body temperature, locomotor activity (LA), feeding, and drinking behaviors were recorded during control and cold conditions at each time-point. Immediately after the stimulus, rats were euthanized and both the soleus and BAT were collected for real-time PCR. RESULTS: During the light phase (i.e., inactive phase), cold exposure resulted in a slight hyperthermia (p < 0.001). Light phase cold exposure also increased metabolic rate and LA (p < 0.001). In addition, the prevalence of fat oxidative metabolism was attenuated during the inactive phase (p < 0.001). These metabolic changes were accompanied by time-of-day and tissue-specific changes in core clock gene expression, such as DBP (p < 0.0001) and REV-ERBα (p < 0.01) in the BAT and CLOCK (p < 0.05), PER2 (p < 0.05), CRY1 (p < 0.05), CRY2 (p < 0.01), and REV-ERBα (p < 0.05) in the soleus skeletal muscle. Moreover, genes involved in substrate oxidation and thermogenesis were affected in a time-of-day and tissue-specific manner by cold exposure. CONCLUSION: The time-of-day modulation of substrate mobilization and oxidation during cold exposure provides a clear example of the circadian modulation of physiological and metabolic responses. Interestingly, after cold exposure, time-of-day mostly affected circadian clock gene expression in the soleus muscle, despite comparable changes in LA over the light–dark-cycle. The current findings add further evidence for tissue-specific actions of the internal clock in different peripheral organs such as skeletal muscle and BAT. |
format | Online Article Text |
id | pubmed-5932155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59321552018-05-11 Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold Machado, Frederico Sander Mansur Zhang, Zhi Su, Yan de Goede, Paul Jansen, Remi Foppen, Ewout Coimbra, Cândido Celso Kalsbeek, Andries Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Daily cyclic changes in environmental conditions are key signals for anticipatory and adaptive adjustments of most living species, including mammals. Lower ambient temperature stimulates the thermogenic activity of brown adipose tissue (BAT) and skeletal muscle. Given that the molecular components of the endogenous biological clock interact with thermal and metabolic mechanisms directly involved in the defense of body temperature, the present study evaluated the differential homeostatic responses to a cold stimulus at distinct time-windows of the light/dark-cycle. METHODS: Male Wistar rats were subjected to a single episode of 3 h cold ambient temperature (4°C) at one of 6 time-points starting at Zeitgeber Times 3, 7, 11, 15, 19, and 23. Metabolic rate, core body temperature, locomotor activity (LA), feeding, and drinking behaviors were recorded during control and cold conditions at each time-point. Immediately after the stimulus, rats were euthanized and both the soleus and BAT were collected for real-time PCR. RESULTS: During the light phase (i.e., inactive phase), cold exposure resulted in a slight hyperthermia (p < 0.001). Light phase cold exposure also increased metabolic rate and LA (p < 0.001). In addition, the prevalence of fat oxidative metabolism was attenuated during the inactive phase (p < 0.001). These metabolic changes were accompanied by time-of-day and tissue-specific changes in core clock gene expression, such as DBP (p < 0.0001) and REV-ERBα (p < 0.01) in the BAT and CLOCK (p < 0.05), PER2 (p < 0.05), CRY1 (p < 0.05), CRY2 (p < 0.01), and REV-ERBα (p < 0.05) in the soleus skeletal muscle. Moreover, genes involved in substrate oxidation and thermogenesis were affected in a time-of-day and tissue-specific manner by cold exposure. CONCLUSION: The time-of-day modulation of substrate mobilization and oxidation during cold exposure provides a clear example of the circadian modulation of physiological and metabolic responses. Interestingly, after cold exposure, time-of-day mostly affected circadian clock gene expression in the soleus muscle, despite comparable changes in LA over the light–dark-cycle. The current findings add further evidence for tissue-specific actions of the internal clock in different peripheral organs such as skeletal muscle and BAT. Frontiers Media S.A. 2018-04-26 /pmc/articles/PMC5932155/ /pubmed/29755411 http://dx.doi.org/10.3389/fendo.2018.00199 Text en Copyright © 2018 Machado, Zhang, Su, de Goede, Jansen, Foppen, Coimbra and Kalsbeek. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Machado, Frederico Sander Mansur Zhang, Zhi Su, Yan de Goede, Paul Jansen, Remi Foppen, Ewout Coimbra, Cândido Celso Kalsbeek, Andries Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title | Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title_full | Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title_fullStr | Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title_full_unstemmed | Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title_short | Time-of-Day Effects on Metabolic and Clock-Related Adjustments to Cold |
title_sort | time-of-day effects on metabolic and clock-related adjustments to cold |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5932155/ https://www.ncbi.nlm.nih.gov/pubmed/29755411 http://dx.doi.org/10.3389/fendo.2018.00199 |
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