In vivo 2H2O administration reveals impaired triglyceride storage in adipose tissue of insulin-resistant humans

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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 classifi ed as insulin resistant (IR) or insulin sensitive (IS). Nondiabetic, moderately obese subjects with BMI 25-35 kg/m2 , classifi ed as IR or IS by the modifi ed insulin suppression test, consumed deuterated water ( 2H2 O) 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 signifi cantly lower in IR as compared with IS subjects, whereas adipocyte proliferation did not differ signifi cantly. 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. -Allister, C. A., L-f. Liu, C. A. Lamendola, C. M. Craig, S. W. Cushman, M. K. Hellerstein, and T. L. McLaughlin. In vivo 2H2 O administration reveals impaired triglyceride storage in adipose tissue of insulinresistant humans. J. Lipid Res.

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Allister, C. A., Liu, L. F., Lamendola, C. A., Craig, C. M., Cushman, S. W., Hellerstein, M. K., & McLaughlin, T. L. (2015). In vivo 2H2O administration reveals impaired triglyceride storage in adipose tissue of insulin-resistant humans. Journal of Lipid Research, 56(2), 435–439. https://doi.org/10.1194/jlr.M052860

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