For their study, the team recruited eight healthy, untrained male volunteers to complete five weeks of high-intensity cycling training. The men worked out three times per week, finishing four minutes of cycling at a target rate of more than 90 per cent of their maximum heart rate followed by a two-minute rest. They repeated this pattern four to five times per workout.
Using a technique called mass spectrometry, the team analysed changes to the composition of 3,168 proteins in tissue samples collected from the participants' thighs before the study and after they completed the training. They also examined changes relating to 1,263 lysine acetyl-sites on 464 acetylated proteins.
Their analyses showed an increase in the production of proteins used to build mitochondria, which produce energy in cells, and in proteins related to muscle contractions. The team also identified increased acetylation of mitochondrial proteins and enzymes that are involved in the production of cellular energy. Additionally, they observed changes in the number of proteins that reduce the skeletal muscle's calcium sensitivity, which is essential for muscle contractions.
The results confirm some well-known changes to skeletal muscle proteins that occur after exercise, as well as identify new ones. For example, the reduced calcium sensitivity may explain why it can be harder for muscle contraction to occur after an athlete becomes fatigued. The work also suggests that exercise-induced changes in the regulation of proteins through acetylation may contribute to boosting metabolism.
"Using state-of-the-art proteomics technology, our study provides new information about how skeletal muscle adapts to exercise training, including the identification of novel exercise-regulated proteins and acetyl-sites," concludes co-corresponding author Atul Deshmukh, associate professor at the Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen. "We hope our work will stimulate further research into how exercise helps improve metabolic health in humans."