Impaired proteostatic mechanisms other than decreased protein synthesis limit old skeletal muscle recovery after disuse atrophy

Bibliographic Details
Title: Impaired proteostatic mechanisms other than decreased protein synthesis limit old skeletal muscle recovery after disuse atrophy
Authors: Jordan D. Fuqua, Marcus M. Lawrence, Zachary R. Hettinger, Agnieszka K. Borowik, Parker L. Brecheen, Marcelina M. Szczygiel, Claire B. Abbott, Frederick F. Peelor III, Amy L. Confides, Michael Kinter, Sue C. Bodine, Esther E. Dupont‐Versteegden, Benjamin F. Miller
Source: Journal of Cachexia, Sarcopenia and Muscle, Vol 14, Iss 5, Pp 2076-2089 (2023)
Publisher Information: Wiley, 2023.
Publication Year: 2023
Collection: LCC:Diseases of the musculoskeletal system
LCC:Human anatomy
Subject Terms: collagen, isotope labelling, protein aggregates, protein turnover, proteomics, ribosome biogenesis, Diseases of the musculoskeletal system, RC925-935, Human anatomy, QM1-695
More Details: Abstract Background Skeletal muscle mass and strength diminish during periods of disuse but recover upon return to weight bearing in healthy adults but are incomplete in old muscle. Efforts to improve muscle recovery in older individuals commonly aim at increasing myofibrillar protein synthesis via mammalian target of rapamycin (mTOR) stimulation despite evidence demonstrating that old muscle has chronically elevated levels of mammalian target of rapamycin complex 1 (mTORC1) activity. We hypothesized that protein synthesis is higher in old muscle than adult muscle, which contributes to a proteostatic stress that impairs recovery. Methods We unloaded hindlimbs of adult (10‐month) and old (28‐month) F344BN rats for 14 days to induce atrophy, followed by reloading up to 60 days with deuterium oxide (D2O) labelling to study muscle regrowth and proteostasis. Results We found that old muscle has limited recovery of muscle mass during reloading despite having higher translational capacity and myofibrillar protein synthesis (0.029 k/day ± 0.002 vs. 0.039 k/day ± 0.002, P
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2190-6009
2190-5991
Relation: https://doaj.org/toc/2190-5991; https://doaj.org/toc/2190-6009
DOI: 10.1002/jcsm.13285
Access URL: https://doaj.org/article/d851fd486f8f4e6f9a75250858a8e346
Accession Number: edsdoj.851fd486f8f4e6f9a75250858a8e346
Database: Directory of Open Access Journals
More Details
ISSN:21906009
21905991
DOI:10.1002/jcsm.13285
Published in:Journal of Cachexia, Sarcopenia and Muscle
Language:English