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Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice
Acute kidney injury (AKI) causes glucose and protein metabolism abnormalities that result in muscle wasting, thereby affecting the long‐term prognosis of critical illness survivors. Here, we examined whether early intervention with treadmill exercise and branched‐chain amino acids (BCAA) can prevent...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448801/ https://www.ncbi.nlm.nih.gov/pubmed/32845566 http://dx.doi.org/10.14814/phy2.14557 |
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author | Nagata, Soichiro Kato, Akihiko Isobe, Shinsuke Fujikura, Tomoyuki Ohashi, Naro Miyajima, Hiroaki Yasuda, Hideo |
author_facet | Nagata, Soichiro Kato, Akihiko Isobe, Shinsuke Fujikura, Tomoyuki Ohashi, Naro Miyajima, Hiroaki Yasuda, Hideo |
author_sort | Nagata, Soichiro |
collection | PubMed |
description | Acute kidney injury (AKI) causes glucose and protein metabolism abnormalities that result in muscle wasting, thereby affecting the long‐term prognosis of critical illness survivors. Here, we examined whether early intervention with treadmill exercise and branched‐chain amino acids (BCAA) can prevent AKI‐related muscle wasting and reduced physical performance in mice. Unilateral 15 min ischemia‐reperfusion injury was induced in contralateral nephrectomized mice, and muscle histological and physiological changes were assessed and compared with those of pair‐fed control mice, since AKI causes severe anorexia. Mice exercised for 30 min each day and received oral BCAA for 7 days after AKI insult. By day 7, ischemic AKI significantly decreased wet weight, myofiber cross‐sectional area, and central mitochondrial volume density of the anterior tibialis muscle, and significantly reduced maximal exercise time. Regular exercise and BCAA prevented AKI‐related muscle wasting and low physical performance by suppressing myostatin and atrogin‐1 mRNA upregulation, and restoring reduced phosphorylated Akt and PGC‐1α mRNA expression in the muscle. Ischemic AKI induces muscle wasting by accelerating muscle protein degradation and reducing protein synthesis; however, we found that regular exercise and BCAA prevented AKI‐related muscle wasting without worsening kidney damage, suggesting that early rehabilitation with nutritional support could prevent AKI‐related muscle wasting. |
format | Online Article Text |
id | pubmed-7448801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74488012020-08-31 Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice Nagata, Soichiro Kato, Akihiko Isobe, Shinsuke Fujikura, Tomoyuki Ohashi, Naro Miyajima, Hiroaki Yasuda, Hideo Physiol Rep Original Research Acute kidney injury (AKI) causes glucose and protein metabolism abnormalities that result in muscle wasting, thereby affecting the long‐term prognosis of critical illness survivors. Here, we examined whether early intervention with treadmill exercise and branched‐chain amino acids (BCAA) can prevent AKI‐related muscle wasting and reduced physical performance in mice. Unilateral 15 min ischemia‐reperfusion injury was induced in contralateral nephrectomized mice, and muscle histological and physiological changes were assessed and compared with those of pair‐fed control mice, since AKI causes severe anorexia. Mice exercised for 30 min each day and received oral BCAA for 7 days after AKI insult. By day 7, ischemic AKI significantly decreased wet weight, myofiber cross‐sectional area, and central mitochondrial volume density of the anterior tibialis muscle, and significantly reduced maximal exercise time. Regular exercise and BCAA prevented AKI‐related muscle wasting and low physical performance by suppressing myostatin and atrogin‐1 mRNA upregulation, and restoring reduced phosphorylated Akt and PGC‐1α mRNA expression in the muscle. Ischemic AKI induces muscle wasting by accelerating muscle protein degradation and reducing protein synthesis; however, we found that regular exercise and BCAA prevented AKI‐related muscle wasting without worsening kidney damage, suggesting that early rehabilitation with nutritional support could prevent AKI‐related muscle wasting. John Wiley and Sons Inc. 2020-08-26 /pmc/articles/PMC7448801/ /pubmed/32845566 http://dx.doi.org/10.14814/phy2.14557 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 Nagata, Soichiro Kato, Akihiko Isobe, Shinsuke Fujikura, Tomoyuki Ohashi, Naro Miyajima, Hiroaki Yasuda, Hideo Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title | Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title_full | Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title_fullStr | Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title_full_unstemmed | Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title_short | Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
title_sort | regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448801/ https://www.ncbi.nlm.nih.gov/pubmed/32845566 http://dx.doi.org/10.14814/phy2.14557 |
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