Short duration small sided football and to a lesser extent whole body vibration exercise induce acute changes in markers of bone turnover

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Joanna L. Bowtell
  • Sarah R Jackman
  • Suzanne Scott
  • Luke J. Connolly
  • Magni Mohr
  • Giorgos Ermidis
  • R Julian
  • F Yousefian
  • Helge, Eva Wulff
  • Niclas Rye Jørgensen
  • J Fulford
  • Karen M. Knapp
  • P Krustrup

We aimed to study whether short-duration vibration exercise or football sessions of two different durations acutely changed plasma markers of bone turnover and muscle strain. Inactive premenopausal women (n = 56) were randomized to complete a single bout of short (FG15) or long duration (FG60) small sided football or low magnitude whole body vibration training (VIB). Procollagen type 1 amino-terminal propeptide (P1NP) was increased during exercise for FG15 (51.6 ± 23.0 to 56.5 ± 22.5 μg·L(-1), mean ± SD, P < 0.05) and FG60 (42.6 ± 11.8 to 50.2 ± 12.8 μg·L(-1), P <0.05) ± (38.8 14.7 μg·l(-1), 15.1 36.6 but for not p to vib> 0.05). An increase in osteocalcin was observed 48 h after exercise (P < 0.05), which did not differ between exercise groups. C-terminal telopeptide of type 1 collagen was not affected by exercise. Blood lactate concentration increased during exercise for FG15 (0.6 ± 0.2 to 3.4 ± 1.2 mM) and FG60 (0.6 ± 0.2 to 3.3 ± 2.0 mM), but not for VIB (0.6 ± 0.2 to 0.8 ± 0.4 mM) (P < 0.05). Plasma creatine kinase increased by 55 ± 63% and 137 ± 119% 48 h after FG15 and FG60 (P < 0.05), but not after VIB (26 ± 54%, NS). In contrast to the minor elevation in osteocalcin in response to a single session of vibration exercise, both short and longer durations of small sided football acutely increased plasma P1NP, osteocalcin, and creatine kinase. This may contribute to favorable effects of chronic training on musculoskeletal health.

OriginalsprogEngelsk
Artikelnummer3574258
TidsskriftBioMed Research International
Vol/bind2016
Antal sider10
ISSN2314-6133
DOI
StatusUdgivet - 2016

Bibliografisk note

CURIS 2016 NEXS 373

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