Dietary fat content alters insulin-mediated glucose metabolism in healthy men

Background: A high dietary fat intake is involved in the pathogenesis of in sulin resistance. Objective: The aim was to compare the effect of different amounts of dietar y fat on hepatic and peripheral insulin sensitivity. Design: Six healthy men were studied on 3 occasions after consuming for 11 d diets with identical energy and protein contents but different percentage s of energy as fat and carbohydrate as follows: 0% and 85% [low-fat, high-c arbohydrate (LFHC) diet], 41% and 44% [intermediate-fat, intermediate-carbo hydrate (IFIC) diet], and 83% and 2% [high-fat, low-carbohydrate (HFLC) die t]. Insulin sensitivity was quantified by using a hyperinsulinemic euglycem ic clamp (plasma insulin concentration: approximate to 190 pmoL/L). Results: During hyperinsulinemia, endogenous glucose production was higher after the HFLC diet (2.5 +/- 0.3 mu mol.kg(-1).min(-1); P < 0.05) than afte r the IFIC and LFHC diets (1.7 +/- 0.3 and 1.2 +/- 0.4 <mu>mol.kg(-1).min(- 1), respectively). The ratio of dietary fat to carbohydrate had no unequivo cal effects on insulin-stimulated glucose uptake. In contrast, insulin-stim ulated, nonoxidative glucose disposal tended to increase in relation to an increase in the ratio of fat to carbohydrate, from 14.8 +/- 5.1 to 20.6 +/- 1.9 to 26.2 +/- 2.9 mu mol.kg(-1).min(-1) (P < 0.074 between the 3 diets). Insulin-stimulated glucose oxidation was significantly lower after the HFL C diet than after the IFIC and LFHC diets: 1.7 +/- 0.3 compared with 13.4 /- 2.1 and 19.0 +/- 2.1 <mu>mol.kg(-1).min(-1), respectively (P < 0.05). Du ring the clamp study, plasma fatty acid concentrations were higher after th e HFLC diet than after the IFIC and LFHC diets: 0.22 +/- 0.02 compared with 0.07 +/- 0.01 and 0.05 +/- 0.01 mmoI/L, respectively (P < 0.05). Conclusion: A high-fat, low-carbohydrate intake reduces the ability of insu lin to suppress endogenous glucose production and alters the relation betwe en oxidative and nonoxidative glucose disposal in a way that favors storage of glucose.