Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men

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Standard

Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men. / Kalsen, Anders; Hostrup, Morten; Söderlund, Karin; Karlsson, Sebastian; Backer, Vibeke; Bangsbo, Jens.

I: Medicine and Science in Sports and Exercise, Bind 48, Nr. 1, 2016, s. 39-48.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kalsen, A, Hostrup, M, Söderlund, K, Karlsson, S, Backer, V & Bangsbo, J 2016, 'Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men', Medicine and Science in Sports and Exercise, bind 48, nr. 1, s. 39-48. https://doi.org/10.1249/MSS.0000000000000732

APA

Kalsen, A., Hostrup, M., Söderlund, K., Karlsson, S., Backer, V., & Bangsbo, J. (2016). Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men. Medicine and Science in Sports and Exercise, 48(1), 39-48. https://doi.org/10.1249/MSS.0000000000000732

Vancouver

Kalsen A, Hostrup M, Söderlund K, Karlsson S, Backer V, Bangsbo J. Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men. Medicine and Science in Sports and Exercise. 2016;48(1):39-48. https://doi.org/10.1249/MSS.0000000000000732

Author

Kalsen, Anders ; Hostrup, Morten ; Söderlund, Karin ; Karlsson, Sebastian ; Backer, Vibeke ; Bangsbo, Jens. / Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men. I: Medicine and Science in Sports and Exercise. 2016 ; Bind 48, Nr. 1. s. 39-48.

Bibtex

@article{513e2dddc275463f84b6127eb8653f8c,
title = "Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men",
abstract = "PURPOSE: The aim of the present study was to investigate the effect of the beta2-agonist terbutaline (TER) on power output and muscle metabolism during maximal sprint cycling.METHODS: In a randomized double-blind crossover design, nine moderately trained men (VO2max: 4.6±0.2 L[BULLET OPERATOR]min) conducted a 10-s cycle sprint after inhalation of either 15 mg TER or placebo (PLA). A muscle biopsy was collected before and <10 s after the sprint, and analyzed for metabolites.RESULTS: Mean and peak power during the sprint were 8.3±1.1 and 7.8±2.5 % higher (P<0.05) in TER than in PLA, respectively. Moreover, net rate of glycogenolysis (6.5±0.8 vs. 3.1±0.7 mmol glucosyl units kg dw s) and glycolysis (2.4±0.2 vs. 1.6±0.2 mmol glucosyl units kg dw s) were higher (P<0.05) in TER than in PLA. After the sprint, ATP was reduced in PLA (P<0.05), but not in TER. During the sprint, there was no difference in breakdown of phosphocreatine (PCr) between treatments. Estimated anaerobic ATP utilization was 9.2 ±4.0 % higher (P<0.05) in TER than in PLA. After the sprint, ATP was lowered (P <0.05) by 25.7±7.3 % in type II fibers in PLA with no reduction in TER. Before the sprint, PCr was 24.5±7.2 % lower (P <0.05) in type II fibers in TER than in PLA. In PLA, breakdown of PCr was 50.2±24.8 % higher (P <0.05) in type II than in type I fibers with no difference in TER.CONCLUSION: The present study shows that a terbutaline-induced increase in power output is associated with increased rates of glycogenolysis and glycolysis in skeletal muscles. Furthermore, as terbutaline counteracted a reduction in ATP in type II fibers, terbutaline may postpone fatigue development in these fibers.",
author = "Anders Kalsen and Morten Hostrup and Karin S{\"o}derlund and Sebastian Karlsson and Vibeke Backer and Jens Bangsbo",
note = "CURIS 2016 NEXS 012",
year = "2016",
doi = "10.1249/MSS.0000000000000732",
language = "English",
volume = "48",
pages = "39--48",
journal = "Medicine and Science in Sports and Exercise",
issn = "0195-9131",
publisher = "Lippincott Williams & Wilkins",
number = "1",

}

RIS

TY - JOUR

T1 - Inhaled Beta2-agonist increases power output and glycolysis during sprinting in men

AU - Kalsen, Anders

AU - Hostrup, Morten

AU - Söderlund, Karin

AU - Karlsson, Sebastian

AU - Backer, Vibeke

AU - Bangsbo, Jens

N1 - CURIS 2016 NEXS 012

PY - 2016

Y1 - 2016

N2 - PURPOSE: The aim of the present study was to investigate the effect of the beta2-agonist terbutaline (TER) on power output and muscle metabolism during maximal sprint cycling.METHODS: In a randomized double-blind crossover design, nine moderately trained men (VO2max: 4.6±0.2 L[BULLET OPERATOR]min) conducted a 10-s cycle sprint after inhalation of either 15 mg TER or placebo (PLA). A muscle biopsy was collected before and <10 s after the sprint, and analyzed for metabolites.RESULTS: Mean and peak power during the sprint were 8.3±1.1 and 7.8±2.5 % higher (P<0.05) in TER than in PLA, respectively. Moreover, net rate of glycogenolysis (6.5±0.8 vs. 3.1±0.7 mmol glucosyl units kg dw s) and glycolysis (2.4±0.2 vs. 1.6±0.2 mmol glucosyl units kg dw s) were higher (P<0.05) in TER than in PLA. After the sprint, ATP was reduced in PLA (P<0.05), but not in TER. During the sprint, there was no difference in breakdown of phosphocreatine (PCr) between treatments. Estimated anaerobic ATP utilization was 9.2 ±4.0 % higher (P<0.05) in TER than in PLA. After the sprint, ATP was lowered (P <0.05) by 25.7±7.3 % in type II fibers in PLA with no reduction in TER. Before the sprint, PCr was 24.5±7.2 % lower (P <0.05) in type II fibers in TER than in PLA. In PLA, breakdown of PCr was 50.2±24.8 % higher (P <0.05) in type II than in type I fibers with no difference in TER.CONCLUSION: The present study shows that a terbutaline-induced increase in power output is associated with increased rates of glycogenolysis and glycolysis in skeletal muscles. Furthermore, as terbutaline counteracted a reduction in ATP in type II fibers, terbutaline may postpone fatigue development in these fibers.

AB - PURPOSE: The aim of the present study was to investigate the effect of the beta2-agonist terbutaline (TER) on power output and muscle metabolism during maximal sprint cycling.METHODS: In a randomized double-blind crossover design, nine moderately trained men (VO2max: 4.6±0.2 L[BULLET OPERATOR]min) conducted a 10-s cycle sprint after inhalation of either 15 mg TER or placebo (PLA). A muscle biopsy was collected before and <10 s after the sprint, and analyzed for metabolites.RESULTS: Mean and peak power during the sprint were 8.3±1.1 and 7.8±2.5 % higher (P<0.05) in TER than in PLA, respectively. Moreover, net rate of glycogenolysis (6.5±0.8 vs. 3.1±0.7 mmol glucosyl units kg dw s) and glycolysis (2.4±0.2 vs. 1.6±0.2 mmol glucosyl units kg dw s) were higher (P<0.05) in TER than in PLA. After the sprint, ATP was reduced in PLA (P<0.05), but not in TER. During the sprint, there was no difference in breakdown of phosphocreatine (PCr) between treatments. Estimated anaerobic ATP utilization was 9.2 ±4.0 % higher (P<0.05) in TER than in PLA. After the sprint, ATP was lowered (P <0.05) by 25.7±7.3 % in type II fibers in PLA with no reduction in TER. Before the sprint, PCr was 24.5±7.2 % lower (P <0.05) in type II fibers in TER than in PLA. In PLA, breakdown of PCr was 50.2±24.8 % higher (P <0.05) in type II than in type I fibers with no difference in TER.CONCLUSION: The present study shows that a terbutaline-induced increase in power output is associated with increased rates of glycogenolysis and glycolysis in skeletal muscles. Furthermore, as terbutaline counteracted a reduction in ATP in type II fibers, terbutaline may postpone fatigue development in these fibers.

U2 - 10.1249/MSS.0000000000000732

DO - 10.1249/MSS.0000000000000732

M3 - Journal article

C2 - 26197029

VL - 48

SP - 39

EP - 48

JO - Medicine and Science in Sports and Exercise

JF - Medicine and Science in Sports and Exercise

SN - 0195-9131

IS - 1

ER -

ID: 141979286