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1Centre of Inflammation and Metabolism, Department of Infectious Diseases and Copenhagen Muscle Research Centre, Rigshospitalet and Faculty of Health Sciences, University of Copenhagen; 2Department of Radiology, Rigshospitalet, University of Copenhagen; and 3Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark
Submitted 25 November 2008 ; accepted in final form 15 February 2009
Glucose ingestion during exercise attenuates activation of metabolic enzymes and expression of important transport proteins. In light of this, we hypothesized that glucose ingestion during training would result in 1) an attenuation of the increase in fatty acid uptake and oxidation during exercise, 2) lower citrate synthase (CS) and β-hydroxyacyl-CoA dehydrogenase (β-HAD) activity and glycogen content in skeletal muscle, and 3) attenuated endurance performance enhancement in the trained state. To investigate this we studied nine male subjects who performed 10 wk of one-legged knee extensor training. They trained one leg while ingesting a 6% glucose solution (Glc) and ingested a sweetened placebo while training the other leg (Plc). The subjects trained their respective legs 2 h at a time on alternate days 5 days a week. Endurance training increased peak power (Pmax) and time to fatigue at 70% of Pmax
14% and
30%, respectively. CS and β-HAD activity increased and glycogen content was greater after training, but there were no differences between Glc and Plc. After training the rate of oxidation of palmitate (Rox) and the % of rate of disappearance that was oxidized (%Rdox) changed. %Rdox was on average 16.4% greater during exercise after training whereas, after exercise %Rdox was 30.4% lower. Rox followed the same pattern. However, none of these parameters were different between Glc and Plc. We conclude that glucose ingestion during training does not alter training adaptation related to substrate metabolism, mitochondrial enzyme activity, glycogen content, or performance.
metabolism; skeletal muscle; performance
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