β2-Adrenergic agonist salbutamol augments hypertrophy in MHCIIa fibers and sprint mean power output but not muscle force during 11 weeks of resistance training in young men

Author:

Jessen Søren1ORCID,Reitelseder Søren2,Kalsen Anders1,Kreiberg Michael1ORCID,Onslev Johan1ORCID,Gad Anders1ORCID,Ørtenblad Niels3ORCID,Backer Vibeke45,Holm Lars26,Bangsbo Jens1ORCID,Hostrup Morten1ORCID

Affiliation:

1. Section of Integrative Physiology, Department of Nutrition, Exercise and Sports, University of Copenhagen, Copenhagen, Denmark

2. Institute of Sports Medicine, Bispebjerg University Hospital, Copenhagen, Denmark

3. Department of Sports Science and Clinical Biomechanics, University of Southern Denmark, Odense, Denmark

4. Centre for Physical Activity Research, Rigshospitalet and University of Copenhagen, Copenhagen Denmark

5. Department of Otorhinolaryngology, Head and Neck Surgery & Audiology, Rigshospitalet and University of Copenhagen, Copenhagen, Denmark

6. School of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham, United Kingdom

Abstract

Here, we show that daily oral treatment with selective β2-agonist salbutamol induces muscle fiber isoform transition from myosin-heavy-chain (MHC)-I toward MHCIIa and augments hypertrophy of MHCIIa fibers during a period of resistance training. Compared with placebo, salbutamol enhanced sprint mean power output, whereas peak power output and measures of muscle strength increased similarly during the resistance training period despite augmented hypertrophy with salbutamol. Thus, salbutamol is a muscle anabolic drug that can enhance sprint ability adaptations to resistance training.

Funder

World Anti-Doping Agency

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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