Two weeks of reduced-volume sprint interval or traditional exercise training does not improve metabolic functioning in sedentary obese men
Open accessAbstract
AIMS: To investigate the effects of short-term, reduced-volume sprint interval training (SIT) compared to traditional exercise recommendations (TER) in sedentary obese men. METHODS: Sixteen subjects [37.8 ± 5.8 years; body mass index (BMI) 32.8 ± 4.7 kg/m(2)] were randomly allocated to 2 weeks of either SIT (6 sessions of 8-12 × 10 s sprints) or TER [10 sessions of 30 min at 65% peak oxygen consumption (VO(2peak))] cycle exercise. Fasting plasma glucose, insulin, non-esterified fatty acids (NEFA), homeostasis model assessment of insulin sensitivity (HOMA-IR), body composition and VO(2peak) were assessed at baseline and approximately 72 h after the final training bout. Skeletal muscle biopsy samples were also obtained before and 72 h after training and analysed for AS160 phosphorylation and COX II, COX IV, GLUT-4, Nur77 and SIRT1 protein expression. RESULTS: No changes in BMI, body composition, VO(2peak), glucose, insulin, NEFA and HOMA-IR were observed after training, either within or between groups. Skeletal muscle markers of glucose metabolism and mitochondrial function also remained unaltered after 2 weeks of exercise training. CONCLUSIONS: Our findings show that 2 weeks of reduced-volume SIT or TER did not elicit any measurable metabolic adaptations in sedentary obese men. Further work is needed to determine the minimal amount of exercise required for short-term adaptations in this population.
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Skleryk et al. reported that a protocol involving 8-12×10 s all-out cycle sprints against 5% body weight interspersed with 80 s rest, performed six times over 2 wk, did not improve mitochondrial capacity in overweight men as reflected by a lack of change in the protein content of COXII and COXIV.
“Skleryk et al. [23] reported that a protocol involving 8–12×10 s all-out cycle sprints against 5% body weight interspersed with 80 s rest, performed six times over 2 wk, did not improve mitochondrial capacity in overweight men as reflected by a lack of change in the protein content of COXII and COXIV.”
From Three minutes of all-out intermittent exercise per week increases skeletal muscle oxidative capacity and improves cardiometabolic health (2014) · cites this paper as [23]
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- Authors
- Skleryk, J. R., Karagounis, L. G., Hawley, J. A., Sharman, M. J., Laursen, P. B., & Watson, G.
- Affiliations
- Edith Cowan University (AU)
- RMIT University (AU)
- Corresponding author
- Skleryk, J. R.
- Venue
- Diabetes Obesity and Metabolism
- Publisher
- Wiley
- Published
- 2013-07-16
- Volume
- 15
- Issue
- 12
- Pages
- 1146-1153
- ISSN
- 1462-8902 (ISSN-L)
- 1463-1326
- OpenAlex
- W2024986074
- Cited by
- 63
- References
- 44
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 4 · 2023: 5 · 2022: 1 · 2021: 5 · 2020: 8 · 2019: 4 · 2018: 8 · 2017: 4 · 2016: 3 · 2015: 11 · 2014: 3 · 2013: 1
- FWCI
- 14.11
- Type
- journal article
- Language
- en
- Open access
- green
- figshare.com
- Locations
- Diabetes Obesity and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Murdoch University Research Portal (submittedVersion)
- eCite Digital Repository (University of Tasmania) (submittedVersion)
- Research Bank (Australian Catholic University) (submittedVersion)
- Edith Cowan University Research Online (Edith Cowan University) (submittedVersion)
- RMIT Research Repository (RMIT University Library) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Figshare (submittedVersion)
- Funders
- Edith Cowan University
- Topics
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Health Sciences › Medicine › Physiology › Physical Activity and Health
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Keywords
- sprint interval training, insulin resistance, glucose metabolism, skeletal muscle glucose transport, GLUT4, AS160 phosphorylation, mitochondrial function, SIRT1, Nur77, free fatty acids, peak oxygen uptake
- MeSH terms
- Adult, Energy Metabolism, Exercise Therapy, Fatty Acids, Nonesterified, Homeostasis, Humans, Insulin, Male, Obesity, Oxygen Consumption, Phosphorylation, Body Mass Index, Muscle, Skeletal, Glucose Transporter Type 4, Sedentary Behavior
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