In vivo 2H2O administration reveals impaired triglyceride storage in adipose tissue of insulin-resistant humans |
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Authors: | Candice A. Allister Li-fen Liu Cindy A. Lamendola Colleen M. Craig Samuel W. Cushman Marc K. Hellerstein Tracey L. McLaughlin |
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Affiliation: | *Department of Nutritional Science and Toxicology, University of California at Berkeley, Berkeley, CA;†Department of Medicine, Stanford University School of Medicine, Stanford, CA;§Diabetes, Endocrinology, and Obesity Branch, National Institute of Digestive Diseases and Kidney Disease, National Institutes of Health, Bethesda, MD |
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Abstract: | Indirect evidence suggests that impaired triglyceride storage in the subcutaneous fat depot contributes to the development of insulin resistance via lipotoxicity. We directly tested this hypothesis by measuring, in vivo, TG synthesis, de novo lipogenesis (DNL), adipocyte proliferation, and insulin suppression of lipolysis in subcutaneous adipose tissue of BMI-matched individuals classified as insulin resistant (IR) or insulin sensitive (IS). Nondiabetic, moderately obese subjects with BMI 25–35 kg/m2, classified as IR or IS by the modified insulin suppression test, consumed deuterated water (2H2O) for 4 weeks. Deuterium incorporation into glycerol, palmitate, and DNA indicated TG synthesis, DNL, and adipocyte proliferation, respectively. Net TG synthesis and DNL in adipose cells were significantly lower in IR as compared with IS subjects, whereas adipocyte proliferation did not differ significantly. Plasma FFAs measured during an insulin suppression test were 2.5-fold higher in IR subjects, indicating resistance to insulin suppression of lipolysis. Adipose TG synthesis correlated directly with DNL but not with proliferation. These results provide direct in vivo evidence for impaired TG storage in subcutaneous adipose tissue of IR as compared with IS. Relative inability to store TG in the subcutaneous depot may represent a mechanism contributing to the development of insulin resistance in the setting of obesity. |
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Keywords: | obesity insulin resistance subcutaneous adipose triglycerides de novo lipogenesis lipolysis |
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