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Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model
Making benefit from the epigenetic effects of environmental factors such as physical activity may result in a considerable improvement in the prevention of chronic civilization diseases. In our chronic swimming rat model, the expression levels of such microRNAs were characterized, that are involved...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897377/ https://www.ncbi.nlm.nih.gov/pubmed/34893938 http://dx.doi.org/10.1007/s10974-021-09612-y |
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author | Gaál, Zsuzsanna Fodor, János Oláh, Attila Radovits, Tamás Merkely, Béla Magyar, János Csernoch, László |
author_facet | Gaál, Zsuzsanna Fodor, János Oláh, Attila Radovits, Tamás Merkely, Béla Magyar, János Csernoch, László |
author_sort | Gaál, Zsuzsanna |
collection | PubMed |
description | Making benefit from the epigenetic effects of environmental factors such as physical activity may result in a considerable improvement in the prevention of chronic civilization diseases. In our chronic swimming rat model, the expression levels of such microRNAs were characterized, that are involved in skeletal muscle differentiation, hypertrophy and fine-tuning of metabolism, which processes are influenced by chronic endurance training, contributing to the metabolic adaptation of skeletal muscle during physical activity. After chronic swimming, the level of miR-128a increased significantly in EDL muscles, which may influence metabolic adaptation and stress response as well. In SOL, the expression level of miR-15b and miR-451 decreased significantly after chronic swimming, which changes are opposite to their previously described increment in insulin resistant skeletal muscle. MiR-451 also targets PGC-1α mRNA, whiches expression level significantly increased in SOL muscles, resulting in enhanced biogenesis and oxidative capacity of mitochondria. In summary, the microRNA expression changes that were observed during our experiments suggest that chronic swim training contributes to a beneficial metabolic profile of skeletal muscle. |
format | Online Article Text |
id | pubmed-8897377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-88973772022-03-08 Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model Gaál, Zsuzsanna Fodor, János Oláh, Attila Radovits, Tamás Merkely, Béla Magyar, János Csernoch, László J Muscle Res Cell Motil Original Paper Making benefit from the epigenetic effects of environmental factors such as physical activity may result in a considerable improvement in the prevention of chronic civilization diseases. In our chronic swimming rat model, the expression levels of such microRNAs were characterized, that are involved in skeletal muscle differentiation, hypertrophy and fine-tuning of metabolism, which processes are influenced by chronic endurance training, contributing to the metabolic adaptation of skeletal muscle during physical activity. After chronic swimming, the level of miR-128a increased significantly in EDL muscles, which may influence metabolic adaptation and stress response as well. In SOL, the expression level of miR-15b and miR-451 decreased significantly after chronic swimming, which changes are opposite to their previously described increment in insulin resistant skeletal muscle. MiR-451 also targets PGC-1α mRNA, whiches expression level significantly increased in SOL muscles, resulting in enhanced biogenesis and oxidative capacity of mitochondria. In summary, the microRNA expression changes that were observed during our experiments suggest that chronic swim training contributes to a beneficial metabolic profile of skeletal muscle. Springer International Publishing 2021-12-10 2022 /pmc/articles/PMC8897377/ /pubmed/34893938 http://dx.doi.org/10.1007/s10974-021-09612-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Gaál, Zsuzsanna Fodor, János Oláh, Attila Radovits, Tamás Merkely, Béla Magyar, János Csernoch, László Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title | Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title_full | Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title_fullStr | Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title_full_unstemmed | Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title_short | Evaluation of muscle-specific and metabolism regulating microRNAs in a chronic swimming rat model |
title_sort | evaluation of muscle-specific and metabolism regulating micrornas in a chronic swimming rat model |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897377/ https://www.ncbi.nlm.nih.gov/pubmed/34893938 http://dx.doi.org/10.1007/s10974-021-09612-y |
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