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Elevated myonuclear density during skeletal muscle hypertrophy in response to training is reversed during detraining

  • Cory M. Dungan
  • , Kevin A. Murach
  • , Kaitlyn K. Frick
  • , Savannah R. Jones
  • , Samuel E. Crow
  • , Davis A. Englund
  • , Ivan J. Vechetti
  • , Vandre C. Figueiredo
  • , Bryana M. Levitan
  • , Jonathan Satin
  • , John J. McCarthy
  • , Charlotte A. Peterson

Producción científica: Articlerevisión exhaustiva

91 Citas (Scopus)

Resumen

Myonuclei gained during exercise-induced skeletal muscle hypertrophy may be long-lasting and could facilitate future muscle adaptability after deconditioning, a concept colloquially termed "muscle memory." The evidence for this is limited, mostly due to the lack of a murine exercise-training paradigm that is nonsurgical and reversible. To address this limitation, we developed a novel progressive weightedwheel- running (PoWeR) model of murine exercise training to test whether myonuclei gained during exercise persist after detraining. We hypothesized that myonuclei acquired during training-induced hypertrophy would remain following loss of muscle mass with detraining. Singly housed female C57BL/6J mice performed 8 wk of PoWeR, while another group performed 8 wk of PoWeR followed by 12 wk of detraining. Age-matched sedentary cage-dwelling mice served as untrained controls. Eight weeks of PoWeR yielded significant plantaris muscle fiber hypertrophy, a shift to a more oxidative phenotype, and greater myonuclear density than untrained mice. After 12 wk of detraining, the plantaris muscle returned to an untrained phenotype with fewer myonuclei. A finding of fewer myonuclei simultaneously with plantaris deconditioning argues against a muscle memory mechanism mediated by elevated myonuclear density in primarily fasttwitch muscle. PoWeR is a novel, practical, and easy-to-deploy approach for eliciting robust hypertrophy in mice, and our findings can inform future research on the mechanisms underlying skeletal muscle adaptive potential and muscle memory.

Idioma originalEnglish
Páginas (desde-hasta)C649-C654
PublicaciónAmerican Journal of Physiology - Cell Physiology
Volumen316
N.º5
DOI
EstadoPublished - 2019

Nota bibliográfica

Publisher Copyright:
Copyright © 2019 the American Physiological Society.

Financiación

Funding for this study was provided by National Institutes of Health Grants AR-071753 (to K. A. Murach), AR-060701 and AG-049806 (to C. A. Peterson and J. J. McCarthy), and AG-046920 (to C. A. Peterson).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)AR-071753, AR-060701, AG-049806
National Institute on AgingR01AG046920

    ASJC Scopus subject areas

    • Physiology
    • Cell Biology

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