Lipid peroxidation and coupled vitamin oxidation in simulated and human gastric fluid inhibited by dietary polyphenols: Health implications

被引:86
作者
Gorelik, S
Lapidot, T
Shaham, I
Granit, R
Ligumsky, M
Kohen, R
Kanner, J [1 ]
机构
[1] Agr Res Org, Volcani Ctr, Dept Food Sci, IL-50250 Bet Dagan, Israel
[2] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Dept Pharmacol, IL-91120 Jerusalem, Israel
[3] Hadassah Univ Hosp, Gastroenterol Unit, IL-91120 Jerusalem, Israel
关键词
lipid peroxidation; vitamins E and C; beta-carotene; human gastric fluid; dietary polyphenois antioxidants; health;
D O I
10.1021/jf040401o
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The Western diet contains large quantities of oxidized lipids, because a large proportion of the food in the diet is consumed in a fried, heated, processed, or stored form. We investigated the reaction that could occur in the acidic pH of the stomach and accelerate the generation of lipid hydroperoxides and cooxidation of dietary vitamins. To estimate the oxygen content in the stomach after food consumption, oxygen released from masticated bread (20 g) into deoxygenated water (100 mL) was measured. Under these conditions, the oxygen concentration rose by 250 mu M and reached a full oxygen saturation. The present study demonstrated that heated red meat homogenized in human gastric fluid, at pH 3.0, generated hydroperoxides and malondialdehyde. The cross-reaction between free radicals produced during this reaction cooxidized vitamin E, P-carotene, and vitamin C. Both lipid peroxiclation and cooxidation of vitamin E and beta-carotene were inhibited at pH 3.0 by red wine polyphenols. Ascorbic acid (44 mg) at a concentration that represented the amount that could be ingested during a meal inhibited lipid peroxiclation only slightly. Red wine polyphenols failed to prevent ascorbic acid oxidation significantly but, in conjunction with ascorbic acid, did inhibit lipid peroxiclation. In the presence of catechin, a well-known polyphenol found in red wine, ascorbic acid at pH 3.0 works in a synergistic manner preventing lipid peroxidation and beta-carotene cooxidation. The present data may explain the major benefits to our health and the crucial role of consuming food products rich in dietary antioxidants such as fruits, vegetables, red wines, or green tea during the meal.
引用
收藏
页码:3397 / 3402
页数:6
相关论文
共 43 条
[1]   OCCURRENCE OF LIPID OXIDATION-PRODUCTS IN FOODS [J].
ADDIS, PB .
FOOD AND CHEMICAL TOXICOLOGY, 1986, 24 (10-11) :1021-1030
[2]   URINARY MALONDIALDEHYDE-EQUIVALENTS DURING INGESTION OF MEAT COOKED AT HIGH OR LOW-TEMPERATURES [J].
BROWN, ED ;
MORRIS, VC ;
RHODES, DG ;
SINHA, R ;
LEVANDER, OA .
LIPIDS, 1995, 30 (11) :1053-1056
[3]  
CHANDHARY AK, 1994, SCIENCE, V265, P1580
[4]   Dietary patterns and adenocarcinoma of the esophagus and distal stomach [J].
Chen, HL ;
Ward, MH ;
Graubard, BI ;
Heineman, EF ;
Markin, RM ;
Potischman, NA ;
Russell, RB ;
Weisenburger, DD ;
Tucker, KL .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 75 (01) :137-144
[5]   Oxidized fat in the diet, postprandial lipaemia and cardiovascular disease [J].
Cohn, JS .
CURRENT OPINION IN LIPIDOLOGY, 2002, 13 (01) :19-24
[6]   ANTIOXIDANT AND CO-ANTIOXIDANT ACTIVITY OF VITAMIN-C - THE EFFECT OF VITAMIN-C, EITHER ALONE OR IN THE PRESENCE OF VITAMIN-E OR A WATER-SOLUBLE VITAMIN-E ANALOG, UPON THE PEROXIDATION OF AQUEOUS MULTILAMELLAR PHOSPHOLIPID LIPOSOMES [J].
DOBA, T ;
BURTON, GW ;
INGOLD, KU .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 835 (02) :298-303
[7]  
*FOOD NUTR BOARD I, 2000, DIET REF INT VIT C V, P1
[8]  
GIOVANNUCCI E, 1994, CANCER RES, V54, P2390
[9]   Guidelines for the systematic treatment of the depressed patient. [J].
Goldfried, MR .
PSYCHOTHERAPY RESEARCH, 2001, 11 (02) :235-236
[10]   In vivo absorption, metabolism, and urinary excretion of au,P-Unsaturated aldehydes in experimental animals - Relevance to the development of cardiovascular diseases by the dietary ingestion of thermally stressed polyunsaturate-rich culinary oils [J].
Grootveld, M ;
Atherton, MD ;
Sheerin, AN ;
Hawkes, J ;
Blake, DR ;
Richens, TE ;
Silwood, CJL ;
Lynch, E ;
Claxson, AWD .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1210-1218