Walnut polyphenolics inhibit in vitro human plasma and LDL oxidation

被引:351
作者
Anderson, KJ
Teuber, SS
Gobeille, A
Cremin, P
Waterhouse, AL
Steinberg, FM [1 ]
机构
[1] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Internal Med, Div Rheumatol Allergy & Clin Immunol, Sch Med, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Viticulture & Enol, Davis, CA 95616 USA
[4] Sequoia Sci, San Diego, CA USA
关键词
polyphenol; ellagic acid; LDL; antioxidant; English walnuts;
D O I
10.1093/jn/131.11.2837
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Recent epidemiologic studies have associated nut consumption with a reduced incidence of cardiovascular mortality. However, little is known about the contribution of nut polyphenols to antioxidant and cardiovascular protection. In this investigation, polyphenol-rich extracts from English walnuts (Juglans regia) were studied and compared with ellagic acid for their ability to inhibit in vitro plasma and LDL oxidation, as well as their effects on LDL a-tocopherol during oxidative stress. In addition, the Trolox equivalent antioxidant activity (TEAC) was determined and liquid chromatography electrospray detection mass spectrometry (LC-ELSD/MS) analyses of the walnut extracts were performed. 2,2'-Azobis'(2-amidino propane) hydrochloride (AAPH)-induced LDL oxidation was significantly inhibited by 87 and 38% with the highest concentration (1.0 mu mol/L) of ellagic acid and walnut extract, respectively. In addition, copper-mediated LDL oxidation was inhibited by 14 and 84% in the presence of ellagic acid and walnut extract, respectively, with a modest, significant LDL alpha -tocopherol sparing effect observed. Plasma thiobarbituric acid reacting substance (TBARS) formation was significantly inhibited by walnut extracts and ellagic acid in a dose-dependent manner, and the extracts exhibited a TEAC value greater than that of alpha -tocopherol. LC-ELSD/MS analysis of the walnut extracts identified ellagic acid monomers, polymeric ellagitannins and other phenolics, principally nonflavonoid compounds. These results demonstrate that walnut polyphenolics are effective inhibitors of in vitro plasma and LDL oxidation. The polyphenolic content of walnuts should be considered when evaluating their antiatherogenic potential.
引用
收藏
页码:2837 / 2842
页数:6
相关论文
共 68 条
[1]   PARTIAL REPLACEMENT OF SATURATED FATTY-ACIDS WITH ALMONDS OR WALNUTS LOWERS TOTAL PLASMA-CHOLESTEROL AND LOW-DENSITY-LIPOPROTEIN CHOLESTEROL [J].
ABBEY, M ;
NOAKES, M ;
BELLING, GB ;
NESTEL, PJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1994, 59 (05) :995-999
[2]   Antioxidant activity of phenolics extracted from Olea europaea L-leaves [J].
Benavente-García, O ;
Castillo, J ;
Lorente, J ;
Ortuño, A ;
Del Rio, JA .
FOOD CHEMISTRY, 2000, 68 (04) :457-462
[3]   The role of oxidized lipoproteins in atherogenesis [J].
Berliner, JA ;
Heinecke, JW .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (05) :707-727
[4]  
BROUSSEAU T, 1993, CLIN CHEM, V39, P960
[5]  
Brown JE, 1998, BIOCHEM J, V330, P1173
[6]  
Buege J A, 1978, Methods Enzymol, V52, P302
[7]   Supplementation with wine phenolic compounds increases the antioxidant capacity of plasma and vitamin E of low-density lipoprotein without changing the lipoprotein Cu2+-oxidizability: Possible explanation by phenolic location [J].
Carbonneau, MA ;
Leger, CL ;
Monnier, L ;
Bonnet, C ;
Michel, F ;
Fouret, G ;
Dedieu, F ;
Descomps, B .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 1997, 51 (10) :682-690
[8]   A diet rich in walnuts favourably influences plasma fatty acid profile in moderately hyperlipidaemic subjects [J].
Chisholm, A ;
Mann, J ;
Skeaff, M ;
Frampton, C ;
Sutherland, W ;
Duncan, A ;
Tiszavari, S .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 1998, 52 (01) :12-16
[9]   The oxidative modification hypothesis of atherogenesis: An overview [J].
Chisolm, GM ;
Steinberg, D .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (12) :1815-1826
[10]   PREDISPOSITION TO LDL OXIDATION IN PATIENTS WITH AND WITHOUT ANGIOGRAPHICALLY ESTABLISHED CORONARY-ARTERY DISEASE [J].
COMINACINI, L ;
GARBIN, U ;
PASTORINO, AM ;
DAVOLI, A ;
CAMPAGNOLA, M ;
DESANTIS, A ;
PASINI, C ;
FACCINI, GB ;
TREVISAN, MT ;
BERTOZZO, L ;
PASINI, F ;
LOCASCIO, V .
ATHEROSCLEROSIS, 1993, 99 (01) :63-70