Key result
Hyperglycemia increases hepatic TG secretion by ~51% while halving splanchnic fatty acid oxidation.
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The effect of hyperglycemia ( approximately 8 mmol/l) on splanchnic fatty acid oxidation and triacylglycerol (TG) secretion rates was investigated in five healthy men. U-13C-labeled fatty acids were infused to estimate fatty acid kinetics and oxidation across the splanchnic region, and in vivo labeled very low density lipoprotein (VLDL)-TG was infused to estimate TG secretion rate. Plasma fatty acid carbon enrichment and concentration were maintained constant by infusion of lipids and heparin in the hyperglycemia experiments. Fatty acid uptake by the splanchnic region was 1.4 +/- 0.2 and 2.2 +/- 0.9 micromol. kg-1. min-1 in the basal and clamp experiments, respectively, whereas fatty acid oxidation decreased from 0.4 +/- 0. 04 to 0.2 +/- 0.05 micromol. kg-1. min-1 (P < 0.05). Hepatic TG secretion increased from 0.35 +/- 0.07 micromol. kg-1. min-1 in the basal state to 0.53 +/- 0.11 micromol. kg-1. min-1 after 15 h of hyperglycemia (P < 0.05). Similarly, plasma VLDL-TG concentration increased from 0.28 +/- 0.06 to 0.43 +/- 0.05 mmol/l during the clamp (P < 0.05). In summary, hyperglycemia attenuates fatty acid oxidation in the splanchnic region in human volunteers, even when fatty acid availability is constant. This adaptation results in a significant increase in the VLDL-TG secretion rate and concentration in plasma.
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Sidossis et al. (1998) studied Healthy men (experimental hyperglycemia) (n=5). Hyperglycemia clamp with constant plasma fatty acid availability (lipids and heparin infusion) vs. Basal state was evaluated on Splanchnic fatty acid oxidation and hepatic triacylglycerol (TG) secretion rates (p=<0.05). Hyperglycemia (8 mmol/l) decreased splanchnic fatty acid oxidation (0.4 to 0.2 umol/kg/min, P<0.05) and increased hepatic TG secretion (0.35 to 0.53 umol/kg/min, P<0.05).
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