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Histological characteristics of exercise‐induced skeletal muscle remodelling
This study aims to analyse the pathological features of skeletal muscle injury repair by using rats to model responses to different exercise intensities. Eighty‐four rats were randomly divided into five groups for treadmill exercise. The short‐term control, low‐intensity, medium‐intensity and high‐i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623533/ https://www.ncbi.nlm.nih.gov/pubmed/37517049 http://dx.doi.org/10.1111/jcmm.17879 |
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author | Su, Qihang Li, Jie Huang, Jingbiao Cai, Qiuchen Xue, Chao Huang, Chenglong Chen, Liyang Li, Jun Li, Dandan Ge, Hengan Cheng, Biao |
author_facet | Su, Qihang Li, Jie Huang, Jingbiao Cai, Qiuchen Xue, Chao Huang, Chenglong Chen, Liyang Li, Jun Li, Dandan Ge, Hengan Cheng, Biao |
author_sort | Su, Qihang |
collection | PubMed |
description | This study aims to analyse the pathological features of skeletal muscle injury repair by using rats to model responses to different exercise intensities. Eighty‐four rats were randomly divided into five groups for treadmill exercise. The short‐term control, low‐intensity, medium‐intensity and high‐intensity groups underwent gastrocnemius muscle sampling after 6, 8 and 12 weeks of exercise. The long‐term high‐intensity group underwent optical coherence tomography angiography and sampling after 18 weeks of exercise. RNA sequencing was performed on the muscle samples, followed by the corresponding histological staining. Differentially expressed genes were generally elevated at 6 weeks in the early exercise stage, followed by a decreasing trend. Meanwhile, the study demonstrated a negative correlation between time and the gene modules involved in vascular regulation. The modules associated with muscle remodelling were positively correlated with exercise intensity. Although the expression of many genes associated with common angiogenesis was downregulated at 8, 12 and 18 weeks, we found that muscle tissue microvessels were still increased, which may be closely associated with elevated sFRP2 and YAP1. During muscle injury‐remodelling, angiogenesis is characterized by significant exercise time and exercise intensity dependence. We find significant differences in the spatial distribution of angiogenesis during muscle injury‐remodelling, which be helpful for the future achievement of spatially targeted treatments for exercise‐induced muscle injuries. |
format | Online Article Text |
id | pubmed-10623533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106235332023-11-04 Histological characteristics of exercise‐induced skeletal muscle remodelling Su, Qihang Li, Jie Huang, Jingbiao Cai, Qiuchen Xue, Chao Huang, Chenglong Chen, Liyang Li, Jun Li, Dandan Ge, Hengan Cheng, Biao J Cell Mol Med Original Articles This study aims to analyse the pathological features of skeletal muscle injury repair by using rats to model responses to different exercise intensities. Eighty‐four rats were randomly divided into five groups for treadmill exercise. The short‐term control, low‐intensity, medium‐intensity and high‐intensity groups underwent gastrocnemius muscle sampling after 6, 8 and 12 weeks of exercise. The long‐term high‐intensity group underwent optical coherence tomography angiography and sampling after 18 weeks of exercise. RNA sequencing was performed on the muscle samples, followed by the corresponding histological staining. Differentially expressed genes were generally elevated at 6 weeks in the early exercise stage, followed by a decreasing trend. Meanwhile, the study demonstrated a negative correlation between time and the gene modules involved in vascular regulation. The modules associated with muscle remodelling were positively correlated with exercise intensity. Although the expression of many genes associated with common angiogenesis was downregulated at 8, 12 and 18 weeks, we found that muscle tissue microvessels were still increased, which may be closely associated with elevated sFRP2 and YAP1. During muscle injury‐remodelling, angiogenesis is characterized by significant exercise time and exercise intensity dependence. We find significant differences in the spatial distribution of angiogenesis during muscle injury‐remodelling, which be helpful for the future achievement of spatially targeted treatments for exercise‐induced muscle injuries. John Wiley and Sons Inc. 2023-07-30 /pmc/articles/PMC10623533/ /pubmed/37517049 http://dx.doi.org/10.1111/jcmm.17879 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Articles Su, Qihang Li, Jie Huang, Jingbiao Cai, Qiuchen Xue, Chao Huang, Chenglong Chen, Liyang Li, Jun Li, Dandan Ge, Hengan Cheng, Biao Histological characteristics of exercise‐induced skeletal muscle remodelling |
title | Histological characteristics of exercise‐induced skeletal muscle remodelling |
title_full | Histological characteristics of exercise‐induced skeletal muscle remodelling |
title_fullStr | Histological characteristics of exercise‐induced skeletal muscle remodelling |
title_full_unstemmed | Histological characteristics of exercise‐induced skeletal muscle remodelling |
title_short | Histological characteristics of exercise‐induced skeletal muscle remodelling |
title_sort | histological characteristics of exercise‐induced skeletal muscle remodelling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623533/ https://www.ncbi.nlm.nih.gov/pubmed/37517049 http://dx.doi.org/10.1111/jcmm.17879 |
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