Effect of lifelong football training on the expression of muscle molecular markers involved in healthy longevity

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • A Mancini
  • D Vitucci
  • G Labruna
  • E Imperlini
  • Morten Bredsgaard Randers
  • Jakob Friis Schmidt
  • H. Hagman
  • Thomas Rostgaard Andersen
  • R Russo
  • S Orrù
  • Peter Krustrup
  • F Salvatore
  • P Buono

PURPOSE: We investigated whether lifelong football training affects the expression of healthy longevity-related muscle molecular markers.

METHODS: Biopsies were collected from the vastus lateralis muscle of 10 lifelong football-trained men (68.2 ± 3.0 years) and of 10 active untrained healthy men (66.7 ± 1.3 years). Gene and protein expression was measured by RTqPCR on RNA and by western blotting on protein extracts from muscle biopsies, respectively.

RESULTS: The expression of AMPKα1/α2, NAMPT, TFAM and PGC1α, which are markers of oxidative metabolism, and MyHC β isoform expression was higher in the muscle of football-trained men vs untrained men. Also citrate synthase activity was higher in trained than in untrained men (109.3 ± 9.2 vs 75.1 ± 9.2 mU/mg). These findings were associated with a healthier body composition in trained than in untrained men [body weight: 78.2 ± 6.5 vs 91.2 ± 11.2 kg; body mass index BMI: 24.4 ± 1.6 vs 28.8 ± 4.0 kg m(-2); fat%: 22.6 ± 8.0 vs 31.4 ± 5.0%)] and with a higher maximal oxygen uptake (VO2max: 34.7 ± 3.8 vs 27.3 ± 4.0 ml/min/kg). Also the expression of proteins involved in DNA repair and in senescence suppression (Erk1/2, Akt and FoxM1) was higher in trained than in untrained men. At BMI- and age-adjusted multiple linear regression analysis, fat percentage was independently associated with Akt protein expression, and VO2max was independently associated with TFAM mRNA and with Erk1/2 protein expression.

CONCLUSIONS: Lifelong football training increases the expression of key markers involved in muscle oxidative metabolism, and in the DNA repair and senescence suppression pathways, thus providing the molecular basis for healthy longevity.

OriginalsprogEngelsk
TidsskriftEuropean Journal of Applied Physiology
Vol/bind117
Udgave nummer4
Sider (fra-til)721-730
Antal sider10
ISSN1439-6319
DOI
StatusUdgivet - 2017

Bibliografisk note

CURIS 2017 NEXS 076

ID: 173948441