Cargando…
The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle
Concurrent training involves a combination of two different modes of training. In this study, we conducted an experiment by combining resistance and endurance training. The purpose of this study was to investigate the influence of the order of concurrent training on signal molecules in skeletal musc...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153037/ https://www.ncbi.nlm.nih.gov/pubmed/32281743 http://dx.doi.org/10.14814/phy2.14411 |
_version_ | 1783521599566118912 |
---|---|
author | Shirai, Takanaga Aoki, Yuki Takeda, Kohei Takemasa, Tohru |
author_facet | Shirai, Takanaga Aoki, Yuki Takeda, Kohei Takemasa, Tohru |
author_sort | Shirai, Takanaga |
collection | PubMed |
description | Concurrent training involves a combination of two different modes of training. In this study, we conducted an experiment by combining resistance and endurance training. The purpose of this study was to investigate the influence of the order of concurrent training on signal molecules in skeletal muscle. The phosphorylation levels of p70 S6 kinase, S6 ribosomal protein, and 4E‐binding protein 1, which are related to hypertrophy signaling, increased significantly in the resistance–endurance order group as compared with in control group not the endurance–resistance order group. The gene expressions related to metabolism were not changed by the order of concurrent training. The mitochondrial respiratory chain complex was evaluated by western blot. Although both groups of concurrent training showed a significant increase in MTCO1, UQCRC2, and ATP5A protein levels, we could not detect a difference based on the order of concurrent training. In conclusion, a concurrent training approach involving resistance training before endurance training on the same day is an effective way to activate both mTOR signaling and mitochondria biogenesis. |
format | Online Article Text |
id | pubmed-7153037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71530372020-04-15 The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle Shirai, Takanaga Aoki, Yuki Takeda, Kohei Takemasa, Tohru Physiol Rep Original Research Concurrent training involves a combination of two different modes of training. In this study, we conducted an experiment by combining resistance and endurance training. The purpose of this study was to investigate the influence of the order of concurrent training on signal molecules in skeletal muscle. The phosphorylation levels of p70 S6 kinase, S6 ribosomal protein, and 4E‐binding protein 1, which are related to hypertrophy signaling, increased significantly in the resistance–endurance order group as compared with in control group not the endurance–resistance order group. The gene expressions related to metabolism were not changed by the order of concurrent training. The mitochondrial respiratory chain complex was evaluated by western blot. Although both groups of concurrent training showed a significant increase in MTCO1, UQCRC2, and ATP5A protein levels, we could not detect a difference based on the order of concurrent training. In conclusion, a concurrent training approach involving resistance training before endurance training on the same day is an effective way to activate both mTOR signaling and mitochondria biogenesis. John Wiley and Sons Inc. 2020-04-13 /pmc/articles/PMC7153037/ /pubmed/32281743 http://dx.doi.org/10.14814/phy2.14411 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals LLC 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 Shirai, Takanaga Aoki, Yuki Takeda, Kohei Takemasa, Tohru The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title | The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title_full | The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title_fullStr | The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title_full_unstemmed | The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title_short | The order of concurrent training affects mTOR signaling but not mitochondrial biogenesis in mouse skeletal muscle |
title_sort | order of concurrent training affects mtor signaling but not mitochondrial biogenesis in mouse skeletal muscle |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153037/ https://www.ncbi.nlm.nih.gov/pubmed/32281743 http://dx.doi.org/10.14814/phy2.14411 |
work_keys_str_mv | AT shiraitakanaga theorderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT aokiyuki theorderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT takedakohei theorderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT takemasatohru theorderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT shiraitakanaga orderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT aokiyuki orderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT takedakohei orderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle AT takemasatohru orderofconcurrenttrainingaffectsmtorsignalingbutnotmitochondrialbiogenesisinmouseskeletalmuscle |