Additive or synergetic effects of phenolic compounds on human low density lipoprotein oxidation

被引:75
作者
Cirico, TL [1 ]
Ornaye, ST [1 ]
机构
[1] Univ Nevada, Dept Nutr, Reno, NV 89557 USA
关键词
LDL oxidation; phenolic compounds; polyphenols; flavonoids; antioxidants;
D O I
10.1016/j.fct.2005.08.025
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The in vitro assessment of the antioxidant capacity of four phenolic compounds; catechin, hesperidin, ferulic acid, and quercetin was evaluated by the examination of their ability to inhibit copper (Cu2+)-mediated human low density lipoprotein (LDL) oxidation by using the thiobarbituric acid-reactive substances (TBARS) assay. Individually, the enrichment of LDLs with various concentrations of catechin, hesperidin, ferulic acid, and quercetin produced both antioxidant and prooxidant effects depending on enrichment concentrations of the polyphenolic compounds. Catechin and hesperidin had predominantly antioxidant effects (51.1%, 76.9%, respectively) while ferulic acid and quercetin had mostly prooxidant effects (166.4%; 191.8%, respectively) on LDL oxidation. However, when the mixture of the four phenolic compounds was used to enrich the LDLs, significant antioxidant capacity was demonstrated at all enrichment levels with a dose-response. Synergistic effects of the polyphenolic compounds as mixtures in preventing human LDL oxidation may reflect that nutritional advantages are found in the consumption of a variety of fruits and vegetables in preventing LDL oxidation and perhaps a host of cardiovascular diseases. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:510 / 516
页数:7
相关论文
共 53 条
[1]  
Alexander RR., 1993, Basic biochemical methods
[2]  
Andrikopoulos Nikolaos K., 2002, Journal of Medicinal Food, V5, P1, DOI 10.1089/109662002753723160
[3]  
[Anonymous], 1988, CIRCULATION, V77, p721A
[4]  
Arts ICW, 2001, AM J CLIN NUTR, V74, P227
[5]  
ASCHERIO A, 1995, J NUTR, V125, pS647
[6]  
Bravo L, 1998, NUTR REV, V56, P317, DOI 10.1111/j.1753-4887.1998.tb01670.x
[7]  
Buege J A, 1978, Methods Enzymol, V52, P302
[8]   Antioxidant and prooxidant behavior of flavonoids: Structure-activity relationships [J].
Cao, GH ;
Sofic, E ;
Prior, RL .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (05) :749-760
[9]  
Cheynier V, 2005, AM J CLIN NUTR, V81, p223S, DOI 10.1093/ajcn/81.1.223S
[10]  
CHUNG BH, 1986, METHOD ENZYMOL, V128, P181