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Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile
BACKGROUND: Exercise, as the cornerstone of pulmonary rehabilitation, is recommended to chronic obstructive pulmonary disease (COPD) patients. The underlying molecular basis and metabolic process were not fully elucidated. METHODS: Sprague-Dawley rats were classified into five groups: non-COPD/rest...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106246/ https://www.ncbi.nlm.nih.gov/pubmed/36752784 http://dx.doi.org/10.1097/CM9.0000000000002175 |
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author | Qumu, Shiwei Sun, Weiliang Guo, Jing Zhang, Yuting Cai, Lesi Si, Chaozeng Xu, Xia Yang, Lulu Situ, Xuanming Yang, Tianyi He, Jiaze Shi, Minghui Liu, Dongyan Ren, Xiaoxia Huang, Ke Niu, Hongtao Li, Hong Yu, Chang’An Chen, Yang Yang, Ting |
author_facet | Qumu, Shiwei Sun, Weiliang Guo, Jing Zhang, Yuting Cai, Lesi Si, Chaozeng Xu, Xia Yang, Lulu Situ, Xuanming Yang, Tianyi He, Jiaze Shi, Minghui Liu, Dongyan Ren, Xiaoxia Huang, Ke Niu, Hongtao Li, Hong Yu, Chang’An Chen, Yang Yang, Ting |
author_sort | Qumu, Shiwei |
collection | PubMed |
description | BACKGROUND: Exercise, as the cornerstone of pulmonary rehabilitation, is recommended to chronic obstructive pulmonary disease (COPD) patients. The underlying molecular basis and metabolic process were not fully elucidated. METHODS: Sprague-Dawley rats were classified into five groups: non-COPD/rest (n = 8), non-COPD/exercise (n = 7), COPD/rest (n = 7), COPD/medium exercise (n = 10), and COPD/intensive exercise (n = 10). COPD animals were exposed to cigarette smoke and lipopolysaccharide instillation for 90 days, while the non-COPD control animals were exposed to room air. Non-COPD/exercise and COPD/medium exercise animals were trained on a treadmill at a decline of 5° and a speed of 15 m/min while animals in the COPD/intensive exercise group were trained at a decline of 5° and a speed of 18 m/min. After eight weeks of exercise/rest, we used ultrasonography, immunohistochemistry, transmission electron microscopy, oxidative capacity of mitochondria, airflow-assisted desorption electrospray ionization-mass spectrometry imaging (AFADESI-MSI), and transcriptomics analyses to assess rectal femoris (RF). RESULTS: At the end of 90 days, COPD rats’ weight gain was smaller than control by 59.48 ± 15.33 g (P = 0.0005). The oxidative muscle fibers proportion was lower (P < 0.0001). At the end of additional eight weeks of exercise/rest, compared to COPD/rest, COPD/medium exercise group showed advantages in weight gain, femoral artery peak flow velocity (Δ58.22 mm/s, 95% CI: 13.85–102.60 mm/s, P = 0.0104), RF diameters (Δ0.16 mm, 95% CI: 0.04–0.28 mm, P = 0.0093), myofibrils diameter (Δ0.06 μm, 95% CI: 0.02–0.10 μm, P = 0.006), oxidative muscle fiber percentage (Δ4.84%, 95% CI: 0.15–9.53%, P = 0.0434), mitochondria oxidative phosphorylate capacity (P < 0.0001). Biomolecules spatial distribution in situ and bioinformatic analyses of transcriptomics suggested COPD-related alteration in metabolites and gene expression, which can be impacted by exercise. CONCLUSION: COPD rat model had multi-level structure and function impairment, which can be mitigated by exercise. |
format | Online Article Text |
id | pubmed-10106246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-101062462023-04-17 Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile Qumu, Shiwei Sun, Weiliang Guo, Jing Zhang, Yuting Cai, Lesi Si, Chaozeng Xu, Xia Yang, Lulu Situ, Xuanming Yang, Tianyi He, Jiaze Shi, Minghui Liu, Dongyan Ren, Xiaoxia Huang, Ke Niu, Hongtao Li, Hong Yu, Chang’An Chen, Yang Yang, Ting Chin Med J (Engl) Original Articles BACKGROUND: Exercise, as the cornerstone of pulmonary rehabilitation, is recommended to chronic obstructive pulmonary disease (COPD) patients. The underlying molecular basis and metabolic process were not fully elucidated. METHODS: Sprague-Dawley rats were classified into five groups: non-COPD/rest (n = 8), non-COPD/exercise (n = 7), COPD/rest (n = 7), COPD/medium exercise (n = 10), and COPD/intensive exercise (n = 10). COPD animals were exposed to cigarette smoke and lipopolysaccharide instillation for 90 days, while the non-COPD control animals were exposed to room air. Non-COPD/exercise and COPD/medium exercise animals were trained on a treadmill at a decline of 5° and a speed of 15 m/min while animals in the COPD/intensive exercise group were trained at a decline of 5° and a speed of 18 m/min. After eight weeks of exercise/rest, we used ultrasonography, immunohistochemistry, transmission electron microscopy, oxidative capacity of mitochondria, airflow-assisted desorption electrospray ionization-mass spectrometry imaging (AFADESI-MSI), and transcriptomics analyses to assess rectal femoris (RF). RESULTS: At the end of 90 days, COPD rats’ weight gain was smaller than control by 59.48 ± 15.33 g (P = 0.0005). The oxidative muscle fibers proportion was lower (P < 0.0001). At the end of additional eight weeks of exercise/rest, compared to COPD/rest, COPD/medium exercise group showed advantages in weight gain, femoral artery peak flow velocity (Δ58.22 mm/s, 95% CI: 13.85–102.60 mm/s, P = 0.0104), RF diameters (Δ0.16 mm, 95% CI: 0.04–0.28 mm, P = 0.0093), myofibrils diameter (Δ0.06 μm, 95% CI: 0.02–0.10 μm, P = 0.006), oxidative muscle fiber percentage (Δ4.84%, 95% CI: 0.15–9.53%, P = 0.0434), mitochondria oxidative phosphorylate capacity (P < 0.0001). Biomolecules spatial distribution in situ and bioinformatic analyses of transcriptomics suggested COPD-related alteration in metabolites and gene expression, which can be impacted by exercise. CONCLUSION: COPD rat model had multi-level structure and function impairment, which can be mitigated by exercise. Lippincott Williams & Wilkins 2023-02-20 2023-02-08 /pmc/articles/PMC10106246/ /pubmed/36752784 http://dx.doi.org/10.1097/CM9.0000000000002175 Text en Copyright © 2023 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Articles Qumu, Shiwei Sun, Weiliang Guo, Jing Zhang, Yuting Cai, Lesi Si, Chaozeng Xu, Xia Yang, Lulu Situ, Xuanming Yang, Tianyi He, Jiaze Shi, Minghui Liu, Dongyan Ren, Xiaoxia Huang, Ke Niu, Hongtao Li, Hong Yu, Chang’An Chen, Yang Yang, Ting Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title | Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title_full | Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title_fullStr | Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title_full_unstemmed | Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title_short | Pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
title_sort | pulmonary rehabilitation restores limb muscle mitochondria and improves the intramuscular metabolic profile |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106246/ https://www.ncbi.nlm.nih.gov/pubmed/36752784 http://dx.doi.org/10.1097/CM9.0000000000002175 |
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