期刊
AMERICAN JOURNAL OF CLINICAL NUTRITION
卷 99, 期 2, 页码 268-275出版社
OXFORD UNIV PRESS
DOI: 10.3945/ajcn.113.069526
关键词
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资金
- Nestec SA
- Swiss National Science Foundation [SNF 31003A_132935, SNF 320030_135743]
- Swiss National Science Foundation (SNF) [320030_135743] Funding Source: Swiss National Science Foundation (SNF)
Background: Epidemiologic and experimental data have suggested that chlorogenic acid, which is a polyphenol contained in green coffee beans, prevents diet-induced hepatic steatosis and insulin resistance. Objective: We assessed whether the consumption of chlorogenic acid rich coffee attenuates the effects of short-term fructose overfeeding, dietary conditions known to increase intrahepatocellular lipids (IHCLs), and blood triglyceride concentrations and to decrease hepatic insulin sensitivity in healthy human. Design: Effects of 3 different coffees were assessed in 10 healthy volunteers in a randomized, controlled, crossover trial. IHCLs, hepatic glucose production (HGP) (by 6,6-d(2) glucose dilution), and fasting lipid oxidation were measured after 14 d of consumption of caffeinated coffee high in chlorogenic acid (C-HCA), decaffeinated coffee high in chlorogenic acid, or decaffeinated coffee with regular amounts of chlorogenic acid (D-RCA); during the last 6 d of the study, the weight-Maintenance diet of subjects was supplemented with 4 g fructose . kg(-1) . d(-1) (total energy intake +/- SD: 143 +/- 1% of weight-maintenance requirements). All participants were also studied without coffee supplementation, either with 4 g fructose . kg(-1) . d(-1) (high fructose only) or without high fructose (control). Results: Compared with the control diet, the high-fructose diet significantly increased IHCLs by 102 +/- 36% and HGP by 16 +/- 3% and decreased fasting. lipid oxidation by 100 +/- 29% (all P < 0.05). All 3 coffees significantly decreased HGP. Fasting lipid oxidation increased with C-HCA and D-RCA (P < 0.05). None of the 3 coffees significantly altered IHCLs. Conclusions: Coffee consumption attenuates hepatic insulin resistance but not the increase of IHCLs induced by fructose overfeeding. This effect does not appear to be mediated by differences in the caffeine or chlorogenic acid content. This trial was registered at clinicaltrials.gov as NCT00827450.
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