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Early morning run-training results in enhanced endurance performance adaptations in mice
Time-of-day differences in acute exercise performance in mice are well established with late active phase (afternoon) runners exhibiting significantly greater endurance performance compared to early active phase (morning) runners. In this study, we asked if performance adaptations would be different...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541096/ https://www.ncbi.nlm.nih.gov/pubmed/37781623 http://dx.doi.org/10.1101/2023.09.18.557933 |
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author | Hesketh, Stuart J. Sexton, Casey L. Wolff, Christopher A. Viggars, Mark R. Esser, Karyn A. |
author_facet | Hesketh, Stuart J. Sexton, Casey L. Wolff, Christopher A. Viggars, Mark R. Esser, Karyn A. |
author_sort | Hesketh, Stuart J. |
collection | PubMed |
description | Time-of-day differences in acute exercise performance in mice are well established with late active phase (afternoon) runners exhibiting significantly greater endurance performance compared to early active phase (morning) runners. In this study, we asked if performance adaptations would be different when training for 6 weeks at two different times of day, and if this corresponds to steady state changes in the phase of peripheral tissue clocks. To address these questions, we endurance trained female PER2::Luciferase mice, at the same relative workload, either in the morning, at ZT13, or in the afternoon, at ZT22. Then, after training, we recorded luminescence from tissues of PER2::Luciferase mice to report timing of tissue clocks in several peripheral tissues. After 6 weeks, we found that both groups exhibited significant improvements in maximal endurance capacity (total treadmill work)(p < 0.0001), but the morning runners exhibited an enhanced rate of adaptation as there was no detectable difference in maximal endurance capacity (p = 0.2182) between the morning and afternoon runners. In addition, morning and afternoon runners exhibited divergent clock phase shifts with a significant 5-hour phase advance in the EDL (p < 0.0001) and soleus (p < 0.0001) of morning runners, but a phase delay in the EDL (p < 0.0001) and Soleus (p < 0.0001) of afternoon runners. Therefore, our data demonstrate that morning training enhances endurance adaptations compared to afternoon training in mice, and we suggest this is due to phase advancement of muscle clocks to better align metabolism with exercise performance. |
format | Online Article Text |
id | pubmed-10541096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105410962023-10-01 Early morning run-training results in enhanced endurance performance adaptations in mice Hesketh, Stuart J. Sexton, Casey L. Wolff, Christopher A. Viggars, Mark R. Esser, Karyn A. bioRxiv Article Time-of-day differences in acute exercise performance in mice are well established with late active phase (afternoon) runners exhibiting significantly greater endurance performance compared to early active phase (morning) runners. In this study, we asked if performance adaptations would be different when training for 6 weeks at two different times of day, and if this corresponds to steady state changes in the phase of peripheral tissue clocks. To address these questions, we endurance trained female PER2::Luciferase mice, at the same relative workload, either in the morning, at ZT13, or in the afternoon, at ZT22. Then, after training, we recorded luminescence from tissues of PER2::Luciferase mice to report timing of tissue clocks in several peripheral tissues. After 6 weeks, we found that both groups exhibited significant improvements in maximal endurance capacity (total treadmill work)(p < 0.0001), but the morning runners exhibited an enhanced rate of adaptation as there was no detectable difference in maximal endurance capacity (p = 0.2182) between the morning and afternoon runners. In addition, morning and afternoon runners exhibited divergent clock phase shifts with a significant 5-hour phase advance in the EDL (p < 0.0001) and soleus (p < 0.0001) of morning runners, but a phase delay in the EDL (p < 0.0001) and Soleus (p < 0.0001) of afternoon runners. Therefore, our data demonstrate that morning training enhances endurance adaptations compared to afternoon training in mice, and we suggest this is due to phase advancement of muscle clocks to better align metabolism with exercise performance. Cold Spring Harbor Laboratory 2023-09-19 /pmc/articles/PMC10541096/ /pubmed/37781623 http://dx.doi.org/10.1101/2023.09.18.557933 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Hesketh, Stuart J. Sexton, Casey L. Wolff, Christopher A. Viggars, Mark R. Esser, Karyn A. Early morning run-training results in enhanced endurance performance adaptations in mice |
title | Early morning run-training results in enhanced endurance performance adaptations in mice |
title_full | Early morning run-training results in enhanced endurance performance adaptations in mice |
title_fullStr | Early morning run-training results in enhanced endurance performance adaptations in mice |
title_full_unstemmed | Early morning run-training results in enhanced endurance performance adaptations in mice |
title_short | Early morning run-training results in enhanced endurance performance adaptations in mice |
title_sort | early morning run-training results in enhanced endurance performance adaptations in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541096/ https://www.ncbi.nlm.nih.gov/pubmed/37781623 http://dx.doi.org/10.1101/2023.09.18.557933 |
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