Effect of beta2-adrenergic agonist and resistance training on maximal oxygen uptake and muscle oxidative enzymes in men

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

While beta2 -adrenoceptor stimulation has been shown to increase lean mass and to alter metabolic properties of skeletal muscle, adaptations in muscle oxidative enzymes and maximal oxygen uptake (V̇O2max) in response to beta2-adrenergic agonist treatment are inadequately explored in humans, particularly in association with resistance training. Herein we investigated beta2-adrenergic-induced changes in V̇O2max, leg and arm composition, and muscle content of oxidative enzymes in response to treatment with the selective beta2-adrenergic agonist terbutaline with and without concurrent resistance training in young men. Forty-six subjects were randomized to four weeks of lifestyle maintenance (n=23) or resistance training (n=23). Within the lifestyle maintenance and resistance training group, subjects received daily terbutaline (8·0.5 mg)(n=13) or placebo (n=10) treatment. No apparent treatment by training interactions were observed during the study period. Terbutaline increased leg and arm lean mass with the intervention, whereas no treatment differences were observed in absolute V̇O2max and incremental peak power output (iPPO). Treatment main effects were observed for V̇O2-reserve (P < .05), V̇O2max relative to body mass (P < .05), V̇O2max relative to leg lean mass (P < .01), and iPPO relative to leg lean mass, in which terbutaline had a negative effect compared to placebo. Furthermore, content of electron transport chain complex I-V decreased by 11% (P < .05) for terbutaline compared to placebo. Accordingly, chronic treatment with the selective beta2-adrenergic agonist terbutaline may negatively affect V̇O2max and iPPO in relative terms, but not in absolute.

OriginalsprogEngelsk
TidsskriftScandinavian Journal of Medicine & Science in Sports
Vol/bind29
Udgave nummer12
Sider (fra-til)1881-1891
Antal sider11
ISSN0905-7188
DOI
StatusUdgivet - 2019

Bibliografisk note

CURIS 2019 NEXS 308

ID: 226827024