The time course of the adaptations of human muscle proteome to bed rest and the underlying mechanisms

• Published in: The Journal of physiology Vol. 590; no. 20; pp. 5211 - 5230
• Main Authors: Brocca, Lorenza, Cannavino, Jessica, Coletto, Luisa, Biolo, Gianni, Sandri, Marco, Bottinelli, Roberto, Pellegrino, Maria Antonietta
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-10-2012; Wiley Subscription Services, Inc; Blackwell Science Inc
• Subjects: Adult; Antioxidants; Autophagy; Bed Rest; Energy Metabolism; Heat-Shock Proteins - metabolism; Humans; Male; Metabolism; Muscle Proteins - metabolism; Muscle, Skeletal - anatomy & histology; Muscle, Skeletal - metabolism; Muscular Disorders, Atrophic - metabolism; Musculoskeletal system; Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha; Protein synthesis; Proteins; Proteome; Skeletal Muscle and Exercise; Sterol Regulatory Element Binding Protein 1 - metabolism; Transcription Factors - metabolism; Young Adult
• ISSN: 0022-3751; 1469-7793
• DOI: 10.1113/jphysiol.2012.240267

Key points
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It is still debated whether an imbalance between production and removal of reactive oxygen species is a major trigger of disuse skeletal muscle atrophy in human limb muscles and what the underlying mechanisms are.
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In the bed rest model of human disuse, redox imbalance, impairment of antioxidant defence systems and metabolic derangement occurred early, before vastus lateralis muscle atrophy developed, and persisted through 35 days of bed rest.
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Down‐regulation of PGC‐1α, a master controller of muscle metabolism, and up‐regulation of SREBP‐1, a master controller of lipid synthesis, are likely to have triggered disuse adaptations through mitochondrial dysfunction, whereas AMP kinase, an energy sensor pathway, was unaltered.
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The present and previous results on the same subjects suggest a causal link between muscle atrophy, impaired skeletal muscle metabolism, impaired whole body oxidative metabolism, and insulin sensitivity and moderate inflammation, which are major risk factors of physical inactivity related diseases.
  In order to get a comprehensive picture of the complex adaptations of human skeletal muscle to disuse and further the understanding of the underlying mechanisms, we participated in two bed rest campaigns, one lasting 35 days and one 24 days. In the first bed rest (BR) campaign, myofibrillar proteins, metabolic enzymes and antioxidant defence systems were found to be down‐regulated both post‐8 days and post‐35 days BR by proteomic analysis of vastus lateralis muscle samples from nine subjects. Such profound alterations occurred early (post‐8 days BR), before disuse atrophy developed, and persisted through BR (post‐35 days BR). To understand the mechanisms underlying the protein adaptations observed, muscle biopsies from the second bed rest campaign (nine subjects) were used to evaluate the adaptations of master controllers of the balance between muscle protein breakdown and muscle protein synthesis (MuRF‐1 and atrogin‐1; Akt and p70S6K), of autophagy (Beclin‐1, p62, LC3, bnip3, cathepsin‐L), of expression of antioxidant defence systems (NRF2) and of energy metabolism (PGC‐1α, SREBP‐1, AMPK). The results indicate that: (i) redox imbalance and remodelling of muscle proteome occur early and persist through BR; (ii) impaired energy metabolism is an early and persistent phenomenon comprising both the oxidative and glycolytic one; (iii) although both major catabolic systems, ubiquitin proteasome and autophagy, could contribute to the progression of atrophy late into BR, a decreased protein synthesis cannot be ruled out; (iv) a decreased PGC‐1α, with the concurrence of SREBP‐1 up‐regulation, is a likely trigger of metabolic impairment, whereas the AMPK pathway is unaltered.