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Relative Workload Determines Exercise-Induced Increases in PGC-1α mRNA

NORDSBORG, NIKOLAI BAASTRUP1,2; LUNDBY, CARSTEN3; LEICK, LOTTE1,4,5; PILEGAARD, HENRIETTE1,4,5

Medicine & Science in Sports & Exercise: August 2010 - Volume 42 - Issue 8 - pp 1477-1484
doi: 10.1249/MSS.0b013e3181d2d21c
Basic Sciences

Introduction: The hypothesis that brief intermittent exercise-induced increases in human skeletal muscle metabolic mRNA is dependent on relative workload was investigated.

Methods: Trained (n = 10) and untrained (n = 8) subjects performed exhaustive intermittent cycling exercise (4 × 4 min at 85% of V˙O2peak, interspersed by 3 min). Trained subjects also performed the intermittent exercise at the same absolute workload as the untrained subjects, corresponding to 70% of V˙O2peak (n = 6).

Results: Exercise at 85% of V˙O2peak elevated (P < 0.001) venous plasma lactate to 10.1 ± 0.4 and 10.8 ± 0.5 mM in the trained and untrained subjects, respectively. Peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) mRNA expression was increased (P < 0.001) approximately four- to fivefold for several hours after exercise in both groups. After exercise at 70% of V˙O2peak, venous plasma lactate was less (P < 0.001) elevated (3.1 ± 0.7 mM) and PGC-1α mRNA content was less (P < 0.05) increased (approximately threefold) than after exercise at 85% of V˙O2peak. Likewise, pyruvate dehydrogenase kinase 4 and hexokinase II mRNA expressions were increased (P < 0.05) only after exercise performed at 85% of V˙O2peak in the trained subjects. Hypoxia-inducible factor 2α mRNA only increased (P < 0.05) 3 h into recovery in trained subjects, with no difference between the 70% and 85% of V˙O2peak trial. No change in hypoxia-inducible factor 1α, phosphofructokinase, citrate synthase, or lactate dehydrogenase, heart and muscle isoforms, mRNA expressions was detected after any of the exercise trials.

Conclusions: The relative intensity of brief intermittent exercise is of major importance for the exercise-induced increase of several mRNA, including PGC-1α.

1Copenhagen Muscle Research Centre, University of Copenhagen, Copenhagen, DENMARK; 2Department of Exercise and Sport Sciences, University of Copenhagen, Copenhagen, DENMARK; 3Rigshospitalet, Copenhagen Muscle Research Centre, Copenhagen, DENMARK; 4Centre of Inflammation and Metabolism, University of Copenhagen, Copenhagen, DENMARK; and 5Department of Biology, University of Copenhagen, Copenhagen, DENMARK

Address for correspondence: Nikolai Baastrup Nordsborg, M.Sc., Ph.D., Copenhagen Muscle Research Centre, University of Copenhagen, Department of Exercise and Sport Sciences, Universitetsparken 13, 2100 Copenhagen, Denmark; E-mail: nnordsborg@ifi.ku.dk.

Submitted for publication July 2009.

Accepted for publication January 2010.

©2010The American College of Sports Medicine