Effects of acute lipid overload on skeletal muscle insulin resistance, metabolic flexibility, and mitochondrial performance
Open accessAbstract
We hypothesized that acute lipid-induced insulin resistance would be attenuated in high-oxidative muscle of lean trained (LT) endurance athletes due to their enhanced metabolic flexibility and mitochondrial capacity. Lean sedentary (LS), obese sedentary (OS), and LT participants completed two hyperinsulinemic euglycemic clamp studies with and without (glycerol control) the coinfusion of Intralipid. Metabolic flexibility was measured by indirect calorimetry as the oxidation of fatty acids and glucose during fasted and insulin-stimulated conditions, the latter with and without lipid oversupply. Muscle biopsies were obtained for mitochondrial and insulin-signaling studies. During hyperinsulinemia without lipid, glucose infusion rate (GIR) was lowest in OS due to lower rates of nonoxidative glucose disposal (NOGD), whereas state 4 respiration was increased in all groups. Lipid infusion reduced GIR similarly in all subjects and reduced state 4 respiration. However, in LT subjects, fat oxidation was higher with lipid oversupply, and although glucose oxidation was reduced, NOGD was better preserved compared with LS and OS subjects. Mitochondrial performance was positively associated with better NOGD and insulin sensitivity in both conditions. We conclude that enhanced mitochondrial performance with exercise is related to better metabolic flexibility and insulin sensitivity in response to lipid overload.
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Under euglycemic-hyperinsulinemic clamp conditions, insulin-resistant states are associated with impaired metabolic flexibility to glucose.
“In those studies, insulin-resistant states are clearly associated with impaired metabolic flexibility to glucose (MetFlex-glu).”
From Metabolic flexibility to lipid availability during exercise is enhanced in individuals with high insulin sensitivity (2018) · cites this paper as [7]
Exercise-enhanced mitochondrial performance is related to a better metabolic flexibility and insulin sensitivity.
“Furthermore, a reduction in mitochondrial oxidative capacity is linked to the development of T2DM and obesity (see “Metabolic syndrome and T2DM”), whereas exercise-enhanced mitochondrial performance is related to a better metabolic flexibility and insulin sensitivity (106) (see “Cancer”).”
From Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease (2018) · cites this paper as [106]
Methodological differences can severely impact interpretation of study data, advocating for a gold-standard application of available methods and technology.
“Methodological differences can severely impact interpretation of study data (106), advocating for a gold-standard application of available methods and technology.”
From Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease (2018) · cites this paper as [106]
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References 50 · Cited by 83
- Authors
- Dubé, J. J., Coen, P. M., DiStefano, G., Chacon, A. C., Helbling, N. L., Desimone, M. E., Stafanovic-Racic, M., Hames, K. C., Despines, A. A., Toledo, F. G. S., & Goodpaster, B. H.
- Affiliations
- University of Pittsburgh (US)
- Sanford Burnham Prebys Medical Discovery Institute (US)
- Division of Endocrinology and Metabolism, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania and
- Corresponding author
- Dubé, John J.
- ORCID
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2014-12-15
- Volume
- 307
- Issue
- 12
- Pages
- E1117-E1124
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- PMC
- PMC4269675
- OpenAlex
- W2104872226
- Cited by
- 83
- References
- 50
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 4 · 2023: 5 · 2022: 5 · 2021: 6 · 2020: 8 · 2019: 6 · 2018: 13 · 2017: 8 · 2016: 8 · 2015: 7
- FWCI
- 3.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (UL1TR000005)
- National Cancer Institute (P30CA138313)
- National Institute of Diabetes and Digestive and Kidney Diseases (K01DK084213, K01-DK-084213-01)
- National Center for Research Resources (P20RR017677, M01-RR00056, M01RR000056)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Keywords
- lipid overload, insulin resistance, skeletal muscle, metabolic flexibility, endurance athletes, Intralipid, hyperinsulinemic-euglycemic clamp, fat oxidation, glucose oxidation, nonoxidative glucose disposal, state 4 respiration, obesity, exercise training, insulin signaling
- MeSH terms
- Adult, Emulsions, Energy Metabolism, Female, Humans, Insulin Resistance, Lipids, Male, Mitochondria, Muscle, Phospholipids, Soybean Oil, Time Factors, Glucose Clamp Technique, Muscle, Skeletal, Cell Respiration, Young Adult
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