Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice

Abstract 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) ca...

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Main Authors: Soichiro Nagata, Akihiko Kato, Shinsuke Isobe, Tomoyuki Fujikura, Naro Ohashi, Hiroaki Miyajima, Hideo Yasuda
Format: Article
Language:English
Published: Wiley 2020-08-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14557
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author Soichiro Nagata
Akihiko Kato
Shinsuke Isobe
Tomoyuki Fujikura
Naro Ohashi
Hiroaki Miyajima
Hideo Yasuda
author_facet Soichiro Nagata
Akihiko Kato
Shinsuke Isobe
Tomoyuki Fujikura
Naro Ohashi
Hiroaki Miyajima
Hideo Yasuda
author_sort Soichiro Nagata
collection DOAJ
description Abstract 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.
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spelling doaj.art-27d72965b508464e8c62152187340fea2022-12-22T01:32:46ZengWileyPhysiological Reports2051-817X2020-08-01816n/an/a10.14814/phy2.14557Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in miceSoichiro Nagata0Akihiko Kato1Shinsuke Isobe2Tomoyuki Fujikura3Naro Ohashi4Hiroaki Miyajima5Hideo Yasuda6Internal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanBlood Purification Unit Hamamatsu University Hospital Hamamatsu JapanInternal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanInternal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanInternal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanInternal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanInternal Medicine 1 Hamamatsu University School of Medicine Hamamatsu JapanAbstract 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.https://doi.org/10.14814/phy2.14557acute kidney injurybranched‐chain amino acidexercisemuscle wasting
spellingShingle Soichiro Nagata
Akihiko Kato
Shinsuke Isobe
Tomoyuki Fujikura
Naro Ohashi
Hiroaki Miyajima
Hideo Yasuda
Regular exercise and branched‐chain amino acids prevent ischemic acute kidney injury‐related muscle wasting in mice
Physiological Reports
acute kidney injury
branched‐chain amino acid
exercise
muscle wasting
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 acute kidney injury
branched‐chain amino acid
exercise
muscle wasting
url https://doi.org/10.14814/phy2.14557
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