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Am J Physiol Endocrinol Metab 274: E321-E327, 1998;
0193-1849/98 $5.00
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Vol. 274, Issue 2, E321-E327, February 1998

Role of human liver lipogenesis and reesterification in triglycerides secretion and in FFA reesterification

Frederique Diraison1 and Michel Beylot1,2

1 Laboratoire de Physiopathologie Métabolique et Rénale and the 2 Centre de Recherche en Nutrition Humaine de Lyon, 69008 Lyon, France

To measure 1) the contribution of hepatic de novo lipogenesis (DNL) and plasma free fatty acid (FFA) reesterification to plasma triglyceride (TG) secretion, and 2) the role of oxidation and hepatic and extrahepatic reesterification in FFA utilization, five normal subjects drank deuterated water and were infused (postabsorptive state) with [1-13C]palmitate and [1,2,3-2H5]glycerol. Total lipid oxidation (Lox) was measured by indirect calorimetry. FFA oxidation (2.76 ± 0.65 µmol · kg-1 · min-1) accounted for 45% of FFA turnover rate (Rt) (1.04 µmol · kg-1 · min-1) and 91% of Lox; FFA reesterification was 3.27 ± 0.54 µmol · kg-1 · min-1. Fractional and absolute TG Rt were 0.21 ± 0.02 h-1 and 0.11 ± 0.05 µmol · kg-1 · min-1. DNL accounted for 3.9 ± 0.9% of TG secretion, and hepatic FFA reesterification accounted for 49.4 ± 5.7%; this last process represented a utilization of FFA of 0.16 ± 0.02 µmol · kg-1 · min-1. We conclude that, in the postabsorptive state, 1) DNL and FFA reesterification account for only 50-55% of TG secretion, the remaining presumably being provided by stored lipids or lipoproteins taken up by liver, 2) most reesterification occurs in extrahepatic tissues, and 3) oxidation and reesterification each contribute about one-half to FFA utilization; FFA oxidation accounts for almost all Lox.

mass spectrometry; indirect calorimetry; oxidation; stable isotopes; lipids


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