This study tested whether a single 100 μg inhalation of salmeterol enhances 12-s sprint performance in both fresh and fatigued states in elite road cyclists. In a randomized crossover design, 16 well-trained, non-asthmatic male cyclists completed 2 trials 1 week apart. Participants inhaled either 100 μg salmeterol or placebo 1h before testing. Each trial involved: an initial 12-s sprint (fresh), a 1h race simulation (40%-95% peak power output) with heart rate, blood lactate concentration, and rating of perceived exertion (RPE) monitored, and a final 12-s sprint (fatigued). Peak and mean power, and vastus lateralis myoelectric activity were recorded during the sprints. Power declined from pre- to post-simulation in both conditions (p < 0.016), but the decrement was attenuated with salmeterol (peak: -7.5% vs. -18.2%; mean: -13.0% vs. -19.8%). Fatigued-sprint peak power was higher with salmeterol (915 ± 135 W) than placebo (831 ± 112 W; p = 0.030), as was mean power (692 ± 76 vs. 643 ± 92 W; p = 0.037). No effect of salmeterol was observed on fresh sprint performance and myoelectric activity. Blood lactate concentration and RPE rose similarly in both conditions (p < 0.001), while heart rate was higher with salmeterol during the first 20 min (p = 0.004). Acute inhalation of salmeterol attenuates muscle fatigue and enhances sprint performance at the end of a simulated race. These findings challenge the presumption of no enhancing effect of inhaled salmeterol at therapeutic doses in competitive road cycling, where final sprints often determine outcomes.

Mitigating End-Stage Fatigue: Acute Inhaled Salmeterol Preserves Sprint Power in Simulated Cycling

Schena, Federico;
2025-01-01

Abstract

This study tested whether a single 100 μg inhalation of salmeterol enhances 12-s sprint performance in both fresh and fatigued states in elite road cyclists. In a randomized crossover design, 16 well-trained, non-asthmatic male cyclists completed 2 trials 1 week apart. Participants inhaled either 100 μg salmeterol or placebo 1h before testing. Each trial involved: an initial 12-s sprint (fresh), a 1h race simulation (40%-95% peak power output) with heart rate, blood lactate concentration, and rating of perceived exertion (RPE) monitored, and a final 12-s sprint (fatigued). Peak and mean power, and vastus lateralis myoelectric activity were recorded during the sprints. Power declined from pre- to post-simulation in both conditions (p < 0.016), but the decrement was attenuated with salmeterol (peak: -7.5% vs. -18.2%; mean: -13.0% vs. -19.8%). Fatigued-sprint peak power was higher with salmeterol (915 ± 135 W) than placebo (831 ± 112 W; p = 0.030), as was mean power (692 ± 76 vs. 643 ± 92 W; p = 0.037). No effect of salmeterol was observed on fresh sprint performance and myoelectric activity. Blood lactate concentration and RPE rose similarly in both conditions (p < 0.001), while heart rate was higher with salmeterol during the first 20 min (p = 0.004). Acute inhalation of salmeterol attenuates muscle fatigue and enhances sprint performance at the end of a simulated race. These findings challenge the presumption of no enhancing effect of inhaled salmeterol at therapeutic doses in competitive road cycling, where final sprints often determine outcomes.
2025
WADA
doping
durability
elite sport
ergogenic aid
physiological resilience
β2‐agonists
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1174862
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