Impaired plasma fatty acid oxidation in extremely obese women
Abstract
Skeletal muscle from extremely obese individuals exhibits decreased lipid oxidation compared with muscle from lean controls. It is unknown whether this effect is observed in vivo or whether the phenotype is preserved after massive weight loss. The objective of this study was to compare free fatty acid (FFA) oxidation during rest and exercise in female subjects who were either lean [ n = 7; body mass index (BMI) = 22.6 ± 2.2 kg/m 2] or extremely obese ( n = 10; BMI = 40.8 ± 5.4 kg/m 2) or postgastric bypass patients who had lost >45 kg (weight reduced) ( n = 6; BMI = 33.7 ± 9.9 kg/m 2) with the use of tracer ([13 C]palmitate and [14 C]acetate) methodology and indirect calorimetry. The lean group oxidized significantly more plasma FFA, as measured by percent fatty acid uptake oxidized, than the extremely obese or weight-reduced group during rest (66.6 ± 14.9 vs. 41.5 ± 16.4 vs. 39.9 ± 15.3%) and exercise (86.3 ± 11.9 vs. 56.3 ± 22.1 vs. 57.3 ± 20.3%, respectively). BMI significantly correlated with percent uptake oxidized during both rest ( r = −0.455) and exercise ( r = −0.459). In conclusion, extremely obese women and weight-reduced women both possess inherent defects in plasma FFA oxidation, which may play a role in massive weight gain and associated comorbidities.
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Reduced capacity for lipid oxidation and activity of mitochondrial enzymes have been found in obese subjects.
“The influence of BMI is supported by others that found reduced capacity for lipid oxidation and activity of mitochondrial enzymes in obese subjects (30,31).”
From Chronological Age Does not Influence<i>Ex-vivo</i>Mitochondrial Respiration and Quality Control in Skeletal Muscle (2016) · cites this paper as [31]
Reduced FA oxidation was observed in obese human muscle.
“While reduced FA oxidation was observed in obese human muscle (39, 42), increased FA oxidation in muscle tissue was found in several HF-fed rodent models (19, 43).”
From Mitochondrial Fission Contributes to Mitochondrial Dysfunction and Insulin Resistance in Skeletal Muscle (2012) · cites this paper as [42]
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References 30 · Cited by 122
- Authors
- Thyfault, J. P., Kraus, R. M., Hickner, R. C., Howell, A. W., Wolfe, R. R., & Dohm, G. L.
- Affiliations
- East Carolina University (US)
- Venue
- American Journal of Physiology-Endocrinology and Metabolism
- Publisher
- American Physiological Society
- Published
- 2004-12
- Volume
- 287
- Issue
- 6
- Pages
- E1076-E1081
- ISSN
- 0193-1849 (ISSN-L)
- 1522-1555
- OpenAlex
- W2100890325
- Cited by
- 122
- References
- 30
- Citations by year
- 2025: 1 · 2024: 3 · 2023: 4 · 2022: 2 · 2021: 3 · 2020: 5 · 2019: 4 · 2018: 5 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 5 · 2013: 10 · 2012: 8
- FWCI
- 4.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Endocrinology and Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (R21AG019209, AG 19209)
- Topics
- Health Sciences › Medicine › Surgery › Bariatric Surgery and Outcomes
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- morbid obesity, women, weight loss, gastric bypass, body mass index, fatty acid uptake, exercise metabolism, obesity-related comorbidities
- MeSH terms
- Adult, Fatty Acids, Female, Hormones, Humans, Kinetics, Middle Aged, Obesity, Morbid, Oxidation-Reduction, Oxygen Consumption, Thinness, Gastric Bypass, Exercise, Body Mass Index, Case-Control Studies
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