Red wine polyphenols, in the absence of alcohol, reduce lipid peroxidative stress in smoking subjects

被引:75
作者
Caccetta, RAA
Burke, V
Mori, TA
Beilin, LJ
Puddey, IB
Croft, KD
机构
[1] Univ Western Australia, Royal Perth Hosp, Dept Med, Perth, WA 6847, Australia
[2] W Australian Heart Res Inst, Perth, WA, Australia
关键词
wine polyphenols; isoprostanes; lipid peroxidation; atherosclerosis; alcohol; free radicals;
D O I
10.1016/S0891-5849(00)00497-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
(P)henolic compounds in red wine can exert antioxidant effects on in vitro lipoprotein oxidation, This has led to speculation that red wine consumption mediates unique anti-atherosclerotic effects compared to other alcoholic beverages. However, studies assessing the effects of red wine consumption on lipoprotein oxidation ex vivo have not been conclusive. The recent identification of the F-2-isoprostanes as oxidative products of arachidonic acid has provided a reliable measure of in vivo lipid peroxidation. This randomized trial investigated changes in plasma and urinary F-2-isoprostane concentrations following red wine, white wine, or dealcoholized red wine consumption in humans, Eighteen male smokers consumed, in random order, red wine, white wine, or dealcoholized red wine, for two weeks with one week washout between beverages. Plasma and urinary F-2-isoprostane concentrations were measured before and alter each beverage. Serum gamma -glutamyl transpeptidase (gamma -GT) and urinary 4-O -methylgallic acid were measured as markers of alcohol consumption and phenolic acid absorption, respectively. Plasma F-2-isoprostanes (p < .05) decreased significantly with dealcoholized red wine but not with the alcohol-containing beverages. Urinary excretion of F-2-isoprostanes showed a similar trend. <gamma>-GT decreased significantly with dealcoholized red wine and increased with both alcohol-containing beverages (p < .01). Urinary excretion of 4-O-methylgallic acid increased significantly (p < .001) in the 24 h urine samples following red wine or dealcoholized red wine ingestion, but not with white wine, Serum urate increased and beta -carotene decreased with both alcoholic beverages relative to dealcoholized red wine. There was no change in the antioxidants alpha- and gamma -tocopherol or vitamin C with any of the beverages. The results suggest that polyphenols in dealcoholized red wine can reduce in vivo lipid peroxidation as measured by F-2-isoprostanes in smoking subjects. However, no reduction in lipid peroxidation was observed following red or white wine consumption, suggesting that any protective effects of wine drinking on cardiovascular disease are unlikely to be related to inhibition of lipid oxidation. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:636 / 642
页数:7
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