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Adipose tissue triglyceride turnover, de novo lipogenesis, and cell proliferation in humans measured with ²H₂O

¹Department of Nutritional Sciences and Toxicology, University of California at Berkeley, Berkeley 94720; and ²Division of Endocrinology and Metabolism, Department of Medicine, San Francisco General Hospital, University of California at San Francisco, San Francisco, California 94110

Submitted 3 March 2003 ; accepted in final form 13 October 2003

The turnover of adipose tissue components (lipids and cells) and the pathways of adipose lipid deposition have been difficult to measure in humans. We apply here a ²H₂O long-term labeling technique for concurrent measurement of adipose-triglyceride (TG) turnover, cell (DNA) proliferation, and de novo lipogenesis (DNL). Healthy subjects drank ²H₂O (70 ml/day) for 5-9 wk. Subcutaneous adipose tissue aspirates were taken (gluteal, thigh, and flank depots). Deuterium incorporation into TG glycerol (representing all-source TG synthesis), TG palmitate (representing DNL, by mass isotopomer distribution analysis), and DNA (representing cell proliferation) was measured by gas chromatography-mass spectrometry. Subjects tolerated the protocol well, and body ²H₂O enrichments were stable. Mean TG-glycerol fractional synthesis was 0.12 (i.e., 12%) with a range of 0.03-0.32 after 5 wk and 0.20 (range 0.08-0.49) after 9 wk (TG half-life 200-270 days). Label decay measurements 5-8 mo after discontinuing ²H₂O gave similar turnover estimates. Net lipolysis (TG turnover) was 50-60 g/day. DNL contribution to adipose-TG was 0.04 after 9 wk, representing 20% of newly deposited TG. Cell proliferation was 0.10-0.17 after 9 wk (half-life 240-425 days). In summary, long-term ²H₂O administration to human subjects allows measurement of the dynamics of adipose tissue components. Turnover of all elements is slow, and DNL contributes 20% of new TG.

triglyceride synthesis; adipogenesis; lipolysis; stable isotopes; lipid kinetics

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