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The Preventive Effect of Specific Collagen Peptides against Dexamethasone-Induced Muscle Atrophy in Miceopen access

Authors
Oh, J.[Oh, J.]Park, S.H.[Park, S.H.]Kim, D.S.[Kim, D.S.]Choi, W.[Choi, W.]Jang, J.[Jang, J.]Rahmawati, L.[Rahmawati, L.]Jang, W.Y.[Jang, W.Y.]Lim, H.K.[Lim, H.K.]Hwang, J.Y.[Hwang, J.Y.]Gu, G.R.[Gu, G.R.]Geum, J.-H.[Geum, J.-H.]Choi, S.-Y.[Choi, S.-Y.]Kim, J.H.[Kim, J.H.]Cho, J.Y.[Cho, J.Y.]
Issue Date
1-Feb-2023
Publisher
MDPI
Keywords
AKT; anti-inflammation; IL-6; mTOR; muscle wasting; myostatin; Smad2
Citation
Molecules, v.28, no.4
Indexed
SCIE
SCOPUS
Journal Title
Molecules
Volume
28
Number
4
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/104542
DOI
10.3390/molecules28041950
ISSN
1420-3049
Abstract
Muscle atrophy, also known as muscle wasting, is the thinning of muscle mass due to muscle disuse, aging, or diseases such as cancer or neurological problems. Muscle atrophy is closely related to the quality of life and has high morbidity and mortality. However, therapeutic options for muscle atrophy are limited, so studies to develop therapeutic agents for muscle loss are always required. For this study, we investigated how orally administered specific collagen peptides (CP) affect muscle atrophy and elucidated its molecular mechanism using an in vivo model. We treated mice with dexamethasone (DEX) to induce a muscular atrophy phenotype and then administered CP (0.25 and 0.5 g/kg) for four weeks. In a microcomputed tomography analysis, CP (0.5 g/kg) intake significantly increased the volume of calf muscles in mice with DEX-induced muscle atrophy. In addition, the administration of CP (0.25 and 0.5 g/kg) restored the weight of the gluteus maximus and the fiber cross-sectional area (CSA) of the pectoralis major and calf muscles, which were reduced by DEX. CP significantly inhibited the mRNA expression of myostatin and the phosphorylation of Smad2, but it did not affect TGF-β, BDNF, or FNDC5 gene expression. In addition, AKT/mTOR, a central pathway for muscle protein synthesis and related to myostatin signaling, was enhanced in the groups that were administered CP. Finally, CP decreased serum albumin levels and increased TNF-α gene expression. Collectively, our in vivo results demonstrate that CP can alleviate muscle wasting through a multitude of mechanisms. Therefore, we propose CP as a supplement or treatment to prevent muscle atrophy. © 2023 by the authors.
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