Altered In Vivo Lipid Fluxes and Cell Dynamics in Subcutaneous Adipose Tissues Are Associated With the Unfavorable Pattern of Fat Distribution in Obese Adolescent Girls

Author:

Nouws Jessica1,Fitch Mark2,Mata Mariana1,Santoro Nicola1ORCID,Galuppo Brittany1,Kursawe Romy3,Narayan Deepak4,Vash-Margita Alla5,Pierpont Bridget1,Shulman Gerald I.678ORCID,Hellerstein Marc2,Caprio Sonia1ORCID

Affiliation:

1. Division of Pediatric Endocrinology, Department of Pediatrics, Yale University School of Medicine, New Haven, CT

2. Department of Nutritional Sciences and Toxicology, University of California at Berkeley, Berkeley, CA

3. Diabetes and Obesity, The Jackson Laboratory, Farmington, CT

4. Division of Plastic and Reconstructive Surgery, Department of Surgery, Yale University School of Medicine, New Haven, CT

5. Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, CT

6. Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT

7. Department of Internal Medicine, Yale University School of Medicine, New Haven, CT

8. Department of Cellular and Molecular Physiology, Yale University, New Haven, CT

Abstract

Patterns of abdominal fat distribution (for example, a high vs. low visceral adipose tissue [VAT]/[VAT + subcutaneous adipose tissue (SAT)] ratio), independent of obesity, during adolescence carry a high risk for insulin resistance and type 2 diabetes. Longitudinal follow-up of a cohort of obese adolescents has recently revealed that a high ratio (high VAT/[VAT + SAT]) is a major determinant of fatty liver and metabolic impairment over time, with these effects being more pronounced in girls than in boys. To unravel the underlying metabolic alterations associated with the unfavorable VAT/(VAT + SAT) phenotype, we used the 2H2O labeling method to measure the turnover of adipose lipids and cells in the subcutaneous abdominal and gluteal/femoral adipose tissue (SAT) of weight-stable obese adolescent girls with a similar level of obesity but discordant VAT/(VAT + SAT) ratios. Girls with the unfavorable (high VAT/[VAT + SAT]) phenotype exhibited higher in vivo rates of triglyceride (TG) turnover (representing both lipolysis and synthesis at steady state), without significant differences in de novo lipogenesis in both abdominal and gluteal depots, compared with obese girls with the favorable phenotype. Moreover, mature adipocytes had higher turnover, with no difference in stromal vascular cell proliferation in both depots in the metabolically unfavorable phenotype. The higher TG turnover rates were significantly correlated with higher intrahepatic fat stores. These findings are contrary to the hypothesis that impaired capacity to deposit TGs or proliferation of new mature adipocytes are potential mechanisms for ectopic fat distribution in this setting. In summary, these results suggest that increased turnover of TGs (lipolysis) and of mature adipocytes in both abdominal and gluteal SAT may contribute to metabolic impairment and the development of fatty liver, even at this very early stage of disease.

Funder

Robert Leet Patterson and Clara Guthrie Patterson Trust

American Diabetes Association

National Institutes of Health

National Institute of Child Health and Human Development

NIH

Bioimage Suite

Diabetes Research Center

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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