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ORIGINAL RESEARCH COMMUNICATION |
1 From the Department of Physiology, University of Lausanne, Lausanne, Switzerland (K-AL, DF, RS, and LT); the University Institute of Social and Preventive Medicine, Lausanne, Switzerland (DF); the Department of Clinical Research, MR Spectroscopy and Methodology, University of Bern, Bern, Switzerland (MI, RK, PV, and CB); the Pennington Biomedical Research Center, Baton Rouge, LA (ER); and the Division of Diabetes, Endocrinology and Metabolism, Lausanne University Hospital, Lausanne, Switzerland (LT)
Background: High fructose consumption is suspected to be causally linked to the epidemics of obesity and metabolic disorders. In rodents, fructose leads to insulin resistance and ectopic lipid deposition. In humans, the effects of fructose on insulin sensitivity remain debated, whereas its effect on ectopic lipids has never been investigated.
Objective: We assessed the effect of moderate fructose supplementation on insulin sensitivity (IS) and ectopic lipids in healthy male volunteers (n = 7).
Design: IS, intrahepatocellular lipids (IHCL), and intramyocellular lipids (IMCL) were measured before and after 1 and 4 wk of a high-fructose diet containing 1.5 g fructose · kg body wt1 · d1. Adipose tissue IS was evaluated from nonesterified fatty acid suppression, hepatic IS from suppression of hepatic glucose output (6,6-2H2-glucose), and muscle IS from the whole-body glucose disposal rate during a 2-step hyperinsulinemic euglycemic clamp. IHCL and IMCL were measured by 1H magnetic resonance spectroscopy.
Results: Fructose caused significant (P < 0.05) increases in fasting plasma concentrations of triacylglycerol (36%), VLDL-triacylglycerol (72%), lactate (49%), glucose (5.5%), and leptin (48%) without any significant changes in body weight, IHCL, IMCL, or IS. IHCL were negatively correlated with triacylglycerol after 4 wk of the high-fructose diet (r = 0.78, P < 0.05).
Conclusion: Moderate fructose supplementation over 4 wk increases plasma triacylglycerol and glucose concentrations without causing ectopic lipid deposition or insulin resistance in healthy humans.
Key Words: Cardiovascular disease risk dyslipidemia healthy men ectopic lipids insulin sensitivity fructose
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