Fourteen days of bed rest induces a decline in satellite cell content and robust atrophy of skeletal muscle fibers in middle-aged adults

Emily J. Arentson-Lantz, Kirk L. English, Douglas Paddon-Jones, Christopher S. Fry

Producción científica: Articlerevisión exhaustiva

152 Citas (Scopus)

Resumen

Bed rest, a ground-based spaceflight analog, induces robust atrophy of skeletal muscle, an effect that is exacerbated with increasing age. We examined the effect of 14 days of bed rest on skeletal muscle satellite cell content and fiber type atrophy in middle-aged adults, an understudied age demographic with few overt signs of muscle aging that is representative of astronauts who perform long-duration spaceflight. Muscle biopsies were obtained from the vastus lateralis of healthy middle-aged adults [n = 7 (4 male, 3 female); age: 51 ± 1 yr] before (Pre-BR) and after (Post-BR) 14 days of bed rest. Immunohistochemical analyses were used to quantify myosin heavy chain (MyHC) isoform expression, cross-sectional area (CSA), satellite cell and myonuclear content, and capillary density. Peak oxygen consumption, knee extensor strength, and body composition were also measured Pre-BR and Post-BR. Post-BR MyHC type 2a fiber percentage was reduced, and mean CSA decreased in all fiber types (-24 ± 5%; P < 0.05). Satellite cell content was also reduced Post-BR (-39 ± 9%; P < 0.05), and the change in satellite cell content was significantly correlated with the change in mean fiber CSA (r2 = 0.60; P < 0.05). A decline in capillary density was observed Post-BR (-23±6%; P<0.05), and Post-BR capillary content was significantly associated with Post-BR peak aerobic capacity (r2 = 0.59; P < 0.05). A subtle decline in myonuclear content occurred during bed rest (-5 ± 1%; P < 0.05). The rapid maladaptation of skeletal muscle to 14 days of mechanical unloading in middle-aged adults emphasizes the need for robust countermeasures to preserve muscle function in astronauts.

Idioma originalEnglish
Páginas (desde-hasta)965-975
Número de páginas11
PublicaciónJournal of Applied Physiology
Volumen120
N.º8
DOI
EstadoPublished - abr 15 2016

Nota bibliográfica

Publisher Copyright:
Copyright © 2016 the American Physiological Society.

Financiación

This work was funded by NSBRI grant NNJ08ZSA002N, NIH R01NR012973 (D. Paddon-Jones), a Texas Space Grant Consortium Fellowship (K. English), NIH grant T32HD007539, and in part by 1UL1RR029876-01 from the National Center for Research Resources. C. Fry is a KL2 scholar supported by the UTMB Claude D. Pepper Older Americans Independence Center NIH/NIA grant P30 AG024832. The study was conducted with the support of UTMB Institute for Translational Sciences, supported in part by a Clinical and Translational Science Award (UL1TR000071) from the National Center for Advancing Translational Sciences (NIH)

FinanciadoresNúmero del financiador
UTMB Claude D. Pepper Older Americans Independence Center NIH
National Institutes of Health (NIH)1UL1RR029876-01, R01NR012973, T32HD007539
National Institute on AgingP30AG024832
National Center for Research Resources
National Center for Advancing Translational Sciences (NCATS)UL1TR000071
National Space Biomedical Research InstituteNNJ08ZSA002N
Institute for Translational Sciences, University of Texas Medical Branch

    ASJC Scopus subject areas

    • Physiology
    • Physiology (medical)

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