Cited by 23Cardiovascular and exercise physiologyMuscle metabolism and nutritionAdipose Tissue and Metabolism

Abdominal fat reducing outcome of exercise training: fat burning or hydrocarbon source redistribution?

Open access
Kuo, Chia-Hua, Harris, M. Brennan·2016·Canadian Journal of Physiology and Pharmacology

Abstract

Fat burning, defined by fatty acid oxidation into carbon dioxide, is the most described hypothesis to explain the actual abdominal fat reducing outcome of exercise training. This hypothesis is strengthened by evidence of increased whole-body lipolysis during exercise. As a result, aerobic training is widely recommended for obesity management. This intuition raises several paradoxes: first, both aerobic and resistance exercise training do not actually elevate 24 h fat oxidation, according to data from chamber-based indirect calorimetry. Second, anaerobic high-intensity intermittent training produces greater abdominal fat reduction than continuous aerobic training at similar amounts of energy expenditure. Third, significant body fat reduction in athletes occurs when oxygen supply decreases to inhibit fat burning during altitude-induced hypoxia exposure at the same training volume. Lack of oxygen increases post-meal blood distribution to human skeletal muscle, suggesting that shifting the postprandial hydrocarbons towards skeletal muscle away from adipose tissue might be more important than fat burning in decreasing abdominal fat. Creating a negative energy balance in fat cells due to competition of skeletal muscle for circulating hydrocarbon sources may be a better model to explain the abdominal fat reducing outcome of exercise than the fat-burning model.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1139/cjpp-2015-0425

Cites

3 of 3 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • The amount of fat lost after a relatively long period of HIIT and SIT is disproportionately larger than the estimated utilization within the HIIT or SIT sessions.

    “As the amount of fat lost after a relatively long period of HIIT and SIT is disproportionately larger than the estimated utilization within the HIIT or SIT sessions, the mechanisms explaining this fat-reducing effect are of interest (Kuo and Harris, 2016).”

    From Effect of Exercise Training on Fat Loss—Energetic Perspectives and the Role of Improved Adipose Tissue Function and Body Fat Distribution (2021) · cites this paper as Kuo and Harris, 2016

    In the section ‘Apparently, aforementioned scientific experiments reject the fat burning hypothesis’ (page unavailable), the paper reports substantial fat reduction after HIIT despite describing it as anaerobic; it also says fat contributes less fuel as exercise intensity rises. That supports the proposed mismatch between fat loss and fat use during exercise, but the copy does not give an estimated session-by-session comparison or address SIT specifically. (LLM, conf=0.82)

    Experimental — accuracy not yet measured
  • HIIT and SIT efficiently reduce total fat mass, despite carbohydrates being the predominant source of energy during exercise bouts.

    “HIIT and SIT also efficiently reduce total fat mass, despite carbohydrates being the predominant source of energy during the exercise bouts (Trapp et al., 2008; Kuo and Harris, 2016).”

    From Effect of Exercise Training on Fat Loss—Energetic Perspectives and the Role of Improved Adipose Tissue Function and Body Fat Distribution (2021) · cites this paper as Kuo and Harris, 2016

    The section headed “Apparently, aforementioned scientific experiments reject the fat burning hypothesis” reports that HIIT reduced total body fat and describes it as anaerobic. Another passage says that exercise becomes more dependent on carbohydrate as intensity increases. Our copy does not separately address sprint interval training (SIT), so it does not support that part of the claim. Page numbers were not provided. (LLM, conf=0.84)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 22

  1. Boudou, P., Sobngwi, E., Mauvais-Jarvis, F., Vexiau, P., and Gautier, J. 2003. Absence of exercise-induced variations in adiponectin levels despite decreased abdominal adiposity and improved insulin sensitivity in type 2 diabetic men. Eur. J. Endocrinol. 149(5): 421-424.
  2. Chin. J. Physiol. 56(1): 18-25.
  3. Coppack, S.W., Fisher, R.M., Gibbons, G.F., Humphreys, S.M., McDonough, M.J., Potts, J.L., and Frayn, K.N. 1990. Postprandial substrate deposition in human forearm and adipose tissues in vivo. Clin. Sci. (London). 79(4): 339-348.
  4. Cribb, P.J., and Hayes, A. 2006. Effects of supplement timing and resistance exercise on skeletal muscle hypertrophy. Med. Sci. Sports Exerc. 38(11): 1918-1925.
  5. Deveci, D., Marshall, J.M., and Egginton, S. 2001. Relationship between capillary angiogenesis, fiber type, and fiber size in chronic systemic hypoxia. Am. J. Physiol. 281(1): H241-H252.
  6. Diaz, M., Martel, N., Fitzsimmons, R.L., Eriksson, N.A., Cowin, G.J., Thomas, G.P., Lê Cao, K.-A., Muscat, G.E.O., and Leong, G.M. 2012. Ski Overexpression in skeletal muscle modulates genetic programs that control susceptibility to diet-induced obesity and insulin signaling. Obesity. 20(11): 2157-2167.
  7. Fouladiun, M., Körner, U., Bosaeus, I., Daneryd, P., Hyltander, A., and Lundholm, K.G. 2005. Body composition and time course changes in regional distribution of fat and lean tissue in unselected cancer patients on palliative care-Correlations with food intake, metabolism, exercise capacity, and hormones. Cancer. 103(10): 2189-2198.
  8. Guo, Y., Ma, L., Enriori, P.J., Koska, J., Franks, P.W., Brookshire, T., Cowley, M.A., Salbe, A.D., DelParigi, A., and Tataranni, P.A. 2006. Physiological evidence for the involvement of peptide YY in the regulation of energy homeostasis in humans. Obesity. 14(9): 1562-1570.
  9. Ivy, J.L., Katz, A.L., Cutler, C.L., Sherman, W.M., and Coyle, E.F. 1988. Muscle glycogen synthesis after exercise: effect of time of carbohydrate ingestion. J. Appl. Physiol. 64(4): 1480-1485.
  10. Ivy, J.L., and Kuo, C.H. 1998. Regulation of GLUT4 protein and glycogen synthase during muscle glycogen synthesis after exercise. Acta Physiol. Scand. 162(3): 295-304. doi: 10.1046/j.1365-201X.1998.0302e.x. · DOI · Paper page
  11. Kuo, C.H., Hunt, D.G., Ding, Z., and Ivy, J.L. 1999. Effect of carbohydrate supplementation on postexercise GLUT-4 protein expression in skeletal muscle. J. Appl. Physiol. 87(6): 2290-2295.
  12. Levenhagen, D.K., Gresham, J.D., Carlson, M.G., Maron, D.J., Borel, M.J., and Flakoll, P.J. 2001. Postexercise nutrient intake timing in humans is critical to recovery of leg glucose and protein homeostasis. Am. J. Physiol. 280(6): E982-993.
  13. Melanson, E.L., Gozansky, W.S., Barry, D.W., Maclean, P.S., Grunwald, G.K., and Hill, J.O. 2009. When energy balance is maintained, exercise does not induce negative fat balance in lean sedentary, obese sedentary, or lean endurance-trained individuals. J. Appl. Physiol. 107(6): 1847-1856. doi: 10.1152/japplphysiol.00958.2009. · DOI
  14. Melanson, E.L., Sharp, T.A., Seagle, H.M., Horton, T.J., Donahoo, W.T., Grunwald, G.K., Hamilton, J.T., and Hill, J.O. 2002b. Effect of exercise intensity on 24-h energy expenditure and nutrient oxidation. J. Appl. Physiol. 92(3): 1045-1052. doi: 10.1152/japplphysiol.00706.2001. · DOI
  15. Romijn, J.A., Klein, S., Coyle, E.F., Sidossis, L.S., and Wolfe, R.R. 1993. Strenuous endurance training increases lipolysis and triglyceride-fatty acid cycling at rest. J. Appl. Physiol. 75(1): 108-113.
  16. Ross, R., and Janssen, I. 2001. Physical activity, total and regional obesity: dose-response considerations. Med. Sci. Sports Exerc. 33(6): S521-S527.
  17. Simsolo, R.B., Ong, J.M., and Kern, P.A. 1993. The regulation of adipose tissue and muscle lipoprotein lipase in runners by detraining. J. Clin. Invest. 92(5): 2124-2130.
  18. Slentz, C.A., Houmard, J.A., and Kraus, W.E. 2009. Exercise, abdominal obesity, skeletal muscle, and metabolic risk: Evidence for a dose response. Obesity. 17(S3): S27-S33. doi: 10.1038/oby.2009.385. · DOI · Paper page
  19. Suzuki, M., Doi, T., Lee, S., Okamura, K., Shimizu, S., Okano, G., Sato, Y., Shimomura, Y., and Fushiki, T. 1999. Effect of meal timing after resistance exercise on hindlimb muscle mass and fat accumulation in trained rats. J. Nutr. Sci. Vitaminol. 45(4): 401-409.
  20. Toth, M.J., Beckett, T., and Poehlman, E.T. 1999. Physical activity and the progressive change in body composition with aging: current evidence and research issues. Med. Sci. Sports Exerc. 31(11): S590-596.
  21. Vissers, D., Hens, W., Taeymans, J., Baeyens, J.-P., Poortmans, J., and Van Gaal, L. 2013. The effect of exercise on visceral adipose tissue in overweight adults: A systematic review and meta-analysis. PLoS ONE. 8(2): e56415. doi: 10.1371/journal.pone.0056415. · DOI · Paper page
  22. Zhu, R., Li, J., Wen, C., Harris, B., Liu, Y.Y., and Kuo, C.H. 2015. Lipid storage changes in human skeletal muscle during detraining. Front. Physiol. 6. doi: 10.3389/fphys.2015.00309. · DOI

Cited by

Sorted by citations

Authors
Kuo, C.-H., & Harris, M. B.
Affiliations
  • China Medical University (TW)
  • William & Mary (US)
Venue
Canadian Journal of Physiology and Pharmacology
Published
2016-07
Volume
94
Issue
7
Pages
695-698
ISSN
  • 0008-4212 (ISSN-L)
  • 1205-7541
OpenAlex
W2290618484
Cited by
23
References
3
Citations by year
2026: 1 · 2025: 1 · 2024: 7 · 2023: 1 · 2022: 3 · 2021: 2 · 2020: 5 · 2018: 2 · 2017: 1
FWCI
2.05
Type
journal article
Language
en
Open access
Locations
  • Canadian Journal of Physiology and Pharmacology (publishedVersion)
  • PubMed (publishedVersion)
  • TSpace (University of Toronto) (acceptedVersion)
Funders
Ministry of Science and Technology, Taiwan
Topics
  • Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
Keywords
abdominal fat reduction, exercise training, fat oxidation, lipolysis, high-intensity intermittent training, aerobic exercise, resistance training, hypoxia, skeletal muscle, adipose tissue, energy balance, obesity treatment
MeSH terms
Adipose Tissue, Animals, Energy Metabolism, Humans, Hydrocarbons, Oxygen Consumption, Exercise, Muscle, Skeletal, Abdominal Fat, Lipid Metabolism, Resistance Training

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review