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  • Mitochondria biogenesis and interval training

Mitochondria biogenesis and interval training

Skeletal muscle is a highly malleable tissue, capable of pronounced metabolic and morphological adaptations in response to contractile activity (i.e. exercise). Repeated sessions of endurance exercise induce marked metabolic and structural adaptations within the skeletal muscle, one of the most striking being the pronounced increase in mitochondrial mass.

The magnitude of this change, or response to training, is dependent on the nature of the training programme. In order to increase the muscle oxidative capacities, continuous (CT) and interval training (IT) are both established exercise modalities used in the preparation of elite athletes as well as in the rehabilitation of patients with chronic diseases.

There is considerable debate as to which training program (CT vs. IT) will have a greater effect on aerobic performance and there are relatively few studies which have directly compared skeletal muscle metabolic adaptations to interval and continuous training.

Mitochondrial biogenesis is a complex process that involved the expression of a large number of genes encoded by both the nuclear and mitochondrial genome, and the molecular events coordinating these expressions within-cell training adaptations remains to be clarified.

Project aims

Our research is interested in the effect of exercise modality on signalling cascades involved in mitochondrial biogenesis

Project findings and impact

Our findings will contribute to the understanding of modality-dependent differences in the cellular adaptations following acute and chronic bouts of exercise.


Research team

Output

A. Combes, J. Dekerle, V. Bougault, F. N. Daussin. Characterization of VO2 Fluctuations during Low-intensity Intermittent Exercise. Eur J Appl Physiol (under review).

A. Combes, J. Dekerle, N. Webborn, P. Watt, V. Bougault, F.N. Daussin.. Metabolic fluctuations influence peroxisome proliferator-activated receptor gamma  coactivator-1 alpha upstream signalling kinases in human skeletal muscle. Am J Physiol Regul Integr Comp Physiol (in preparation).

Partners

Dr Frederic Daussin (University of Lille; France)
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