Journal
EUROPEAN JOURNAL OF CLINICAL NUTRITION
Volume 55, Issue 5, Pages 334-341Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.ejcn.1601161
Keywords
phenols; tyrosol; hydroxytyrosol; oleuropein; olive oil; antioxidants; LDL-oxidation; HDL-oxidation; lipid hydroperoxides; malondialdehyde; protein carbonyls; FRAP
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Objective: We studied whether consumption of phenol-rich extra virgin olive oil affects the susceptibility of low density lipoproteins (LDL) to oxidation and other markers of oxidation in humans. Design: Randomized cross-over intervention trial, stratified according to sex, age and energy intake. Setting: Division of Human Nutrition and Epidemiology, Wageningen University, The Netherlands. Subjects: Forty-six health. mon and nomen completed the study. Intervention: Subjects consumed two diets supplying 69 g per day of extra virgin olive oil either rich or poor in phenols for 3 weeks each. The mean difference in phenol intake between the treatments was 18 me pel day. Vitamin E intake cas low during the whole study. Fasting blood samples were taken twice at the end of each Results: Resistance of LDL and high density lipoprotein (HDL) to oxidation was not affected by treatment. Thr mean lag time of copper-induced formation of conjugated dienes was 1.6 min shorter in LDL and 0.4 min longer in HDL after the high phenol diet. Other markers of antioxidant capacity in plasma were also not affected: mean lipid hydroperoxides were 0.07 mu mol/l higher, mean malondialdehyde were 0.001 mu mol/l higher, tnc an protein carbonyls were 0.001 nmol/mg protein lower, and the mean ferric reducing ability of plasma (FRAP) was 0.006 mmol/l higher after the high phenol diet. Ali 95% confidence intervals enclosed zero. Serum cholesterol concentrations were not affected by the treatment. Conclusion: Consumption of 18 mg per day of phenols from extra virgin olive oil for 3 weeks did wt affect LDL a: HDL oxidation or other markers of antioxidant capacity in fasting plasma samples.
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