Mechanisms underlying enhancements in muscle force and power output during maximal cycle ergometer exercise induced by chronic β2-adrenergic stimulation in men

Morten Hostrup, Anders Kalsen, Johan Onslev, Søren Jessen, Christoffer Haase, Sajad Habib, Niels Ørtenblad, Vibeke Backer, Jens Bangsbo

25 Citations (Scopus)

Abstract

The study was a randomized placebo-controlled trial investigating mechanisms by which chronic β2 -adrenergic stimulation enhances muscle force and power output during maximal cycle ergometer exercise in young men. Eighteen trained men were assigned to an experimental group [oral terbutaline 5 mg/30 kg body weight (bw) twice daily (TER); n= 9] or a control group [placebo (PLA); n= 9] for a 4-wk intervention. No changes were observed with the intervention in PLA. Isometric muscle force of the quadriceps increased (P ≤ 0.01) by 97 ± 29 N (means ± SE) with the intervention in TER compared with PLA. Peak and mean power output during 30 s of maximal cycling increased (P ± 0.01) by 32 ± 8 and 25 ± 9 W, respectively, with the intervention in TER compared with PLA. Maximal oxygen consumption (V O2max ) and time to fatigue during incremental cycling did not change with the intervention. Lean body mass increased by 1.95 ± 0.8 kg (P ≤ 0.05) with the intervention in TER compared with PLA. Change in single fiber cross-sectional area of myosin heavy chain (MHC) I (1,205 ± 558μm-2 ; P ≤ 0.01) and MHC II fibers (1,277 ± 595 μm2 ; P≤ 0.05) of the vastus lateralis muscle was higher for TER than PLA with the intervention, whereas no changes were observed in MHC isoform distribution. Expression of muscle proteins involved in growth, ion handling, lactate production, and clearance increased (P ± 0.05) with the intervention in TER compared with PLA, with no change in oxidative enzymes. Our observations suggest that muscle hypertrophy is the primary mechanism underlying enhancements in muscle force and peak power during maximal cycling induced by chronic β;-adrenergic stimulation in humans.

Original languageEnglish
JournalJournal of Applied Physiology
Volume119
Issue number5
Pages (from-to)475-486
Number of pages12
ISSN8750-7587
DOIs
Publication statusPublished - 1 Sept 2015

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