4.7 Article

Effects of oxidative stress on endothelial function after a high-fat meal

Journal

CLINICAL SCIENCE
Volume 106, Issue 3, Pages 315-319

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/CS20030227

Keywords

endothelial function; flow-mediated vasodilatation; glutathione peroxidase; high-fat meal; oxidative stress; postprandial hypertriglyceridaemia

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Postprandial lipaemia is known to cause endothelial dysfunction, but its underlying mechanism is still under debate. The present study was undertaken to investigate the effects of postprandial lipaemia on endothelial dysfunction and oxidative stress. We measured plasma glutathione peroxidase (GSH-Px), an antioxidant enzyme, and the urinary excretion of 8-epi-prostaglandin F-2alpha (8-PGF(2alpha)), a free radical-catalysed product from the oxidative modification of arachiclonic acid, in 16 healthy subjects (mean age, 30 +/- 5 years) without major coronary risk factors. Plasma high-sensitive C-reactive protein, soluble intercellular cell-adhesion molecule-I and vascular cell-adhesion molecule-I were also measured. High-resolution ultrasound was used to assess the flowmediated vasodilatation (FMD) of the brachial artery. Blood and urine samples were collected before and 2, 4 and 6 h after a standard high-fat meal (3677 J, containing 50 g of fat). Serum triacylglycerol (triglyceride) increased and FMD decreased significantly after a high-fat meal. Plasma GSH-Px significantly decreased from 27.2 +/- 12.3 mug/ml to 25.7 +/- 11.8 mug/ml (P = 0.022) 2 h after the meal, and urinary excretion of 8-PGF(2alpha) significantly increased from 1286 +/- 1401 pg/mg of creatinine to 2 197 +/- 1343 pg/mg of creatinine (P = 0.014) at 4 h after the meal. However, there were no significant changes in the levels of high-sensitive C-reactive protein and adhesion molecules after a high-fat meal. In conclusion, endothelial dysfunction was observed after consuming a high-fat meal and is associated with augmented oxidative stress manifested by the depletion of serum antioxidant enzymes and increased excretion of oxidative modification products.

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