Abstract
Introduction Many athletes use short-acting inhaled beta2-agonists multiple times weekly during training sessions to prevent exercise-induced bronchoconstriction, but it is unclear if treatment impairs training outcomes. Herein, we investigated performance adaptations in well-trained females and males training with prior inhalation of salbutamol.
Methods Nineteen females and 21 males with maximal oxygen uptake (VO2max) of 50.5±3.3 and 57.9±4.9 mL·min−1·kg−1 participated in this double-blinded, placebo-controlled, parallel-group study. We randomised participants to placebo or salbutamol inhalation (1600 µg·training day−1) for 6 weeks of combined endurance (1×/week) and high-intensity interval-training (2×/week). We assessed participants’ body composition, VO2max, and muscle contractile function, and collected vastus lateralis muscle biopsies.
Results Salbutamol induced a sex-specific loss of whole-body fat mass (sex×treatment: p=0.048) where only salbutamol-treated females had a fat mass reduction compared to placebo (–0.8 kg at 6 weeks; 95%CI: −0.5 to −1.6; p=0.039). Furthermore, salbutamol-treated females exhibited a repartitioning effect, lowering fat mass while gaining lean mass (p=0.011), which was not apparent for males (p=0.303). Salbutamol negatively impacted VO2max in both sexes (treatment main-effect: p=0.014) due to a blunted increase in VO2max during the initial 4 weeks of the intervention. Quadriceps contractile strength was impaired in salbutamol-treated females (−39 Nm; 95%CI: −61 to −17; p=0.002) compared to placebo at 6 weeks. Muscle electron-transport-chain complex I-V abundance increased with salbutamol (treatment main-effect: p=0.035) while content of SERCAI, beta2-adrenoceptor, and desmin remained unchanged.
Conclusion Inhaled salbutamol appears to be an effective repartitioning agent in females but may impair aerobic and strength related training outcomes.
Footnotes
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- Received September 5, 2023.
- Accepted October 24, 2023.
- Copyright ©The authors 2023
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