Effect of tea flavonoid supplementation on the susceptibility of low-density lipoprotein to oxidative modification

被引:224
作者
Ishikawa, T [1 ]
Suzukawa, M [1 ]
Ito, T [1 ]
Yoshida, H [1 ]
Ayaori, M [1 ]
Nishiwaki, M [1 ]
Yonemura, A [1 ]
Hara, Y [1 ]
Nakamura, H [1 ]
机构
[1] MITUI NORIN CO,FOOD RES LABS,SHIZUOKA,JAPAN
关键词
tea flavonoids; catechin; theaflavins; low-density lipoprotein; LDL; oxidation; macrophage; atherosclerosis; epicatechin; epigallocatechin; epicatechin gallate; epigallocatechin gallate; theaflavin monogallate; theaflavin digallate; humans;
D O I
10.1093/ajcn/66.2.261
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
Dietary flavonoid intake has been reported to be inversely associated with the incidence of coronary artery disease. To clarify the possible role of tea flavonoids in the prevention of atherosclerosis, we investigated the effects of tea flavonoids on the susceptibility of low-density lipoprotein (LDL) to oxidative modification. In an in vitro study, catechins or theaflavins (25-400 mu mol/L) were added to plasma and incubated for 3 h at 37 degrees C. Then, the LDL fraction was separated by ultracentrifugation. The oxidizability of LDL was estimated by measuring conjugated diene, thiobarbituric acid-reactive substances (TEARS), and lipid peroxides after cupric sulfate was added. TEARS and lipid peroxides in the supernates were also measured after incubation with macrophages. Catechins significantly (P < 0.01 by ANOVA) and dose-dependently prolonged the lag time before initiation of oxidation. Among the catechins, epigallocatechin gallate exerted the most marked effect, prolonging the oxidation lag time more than vitamin E at the same molar concentration. Theaflavins exerted stronger inhibitory effects than catechins. Macrophage-mediated LDL oxidation was also inhibited by adding these tea flavonoids to the plasma samples. In an in vivo study, 14 healthy volunteers consumed 750 mt black tea/d for 4 wk. After the subjects had consumed tea for 4 wk, the lag time before LDL oxidation was significantly (P < 0.01) prolonged from 54 to 62 min. This minor prolongation occurred despite much lower plasma flavonoids than were used in vitro. No significant change was observed in eight control volunteers. LDL exposed to tea flavonoids in vitro or in vivo reduced oxidizability. We speculate that tea flavonoids may have a role in ameliorating atherosclerosis.
引用
收藏
页码:261 / 266
页数:6
相关论文
共 31 条
[1]   ANTIOXIDANT VITAMINS AND LOW-DENSITY-LIPOPROTEIN OXIDATION [J].
ABBEY, M ;
NESTEL, PJ ;
BAGHURST, PA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1993, 58 (04) :525-532
[2]   CHELATING AND FREE-RADICAL SCAVENGING MECHANISMS OF INHIBITORY-ACTION OF RUTIN AND QUERCETIN IN LIPID-PEROXIDATION [J].
AFANASEV, IB ;
DOROZHKO, AI ;
BRODSKII, AV ;
KOSTYUK, VA ;
POTAPOVITCH, AI .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (11) :1763-1769
[3]  
Buege J A, 1978, Methods Enzymol, V52, P302
[4]  
CHUNG BH, 1986, METHOD ENZYMOL, V128, P181
[5]   Red wine consumption does not affect oxidizability of low-density lipoproteins in volunteers [J].
deRijke, YB ;
Demacker, PNM ;
Assen, NA ;
Sloots, LM ;
Katan, MB ;
Stalenhoef, AFH .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1996, 63 (03) :329-334
[6]   FLAVONOIDS INHIBIT THE OXIDATIVE MODIFICATION OF LOW-DENSITY LIPOPROTEINS BY MACROPHAGES [J].
DEWHALLEY, CV ;
RANKIN, SM ;
HOULT, JRS ;
JESSUP, W ;
LEAKE, DS .
BIOCHEMICAL PHARMACOLOGY, 1990, 39 (11) :1743-1750
[7]   CONTINUOUS MONITORING OF INVITRO OXIDATION OF HUMAN LOW-DENSITY LIPOPROTEIN [J].
ESTERBAUER, H ;
STRIEGL, G ;
PUHL, H ;
ROTHENEDER, M .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 6 (01) :67-75
[8]   INHIBITION OF OXIDATION OF HUMAN LOW-DENSITY-LIPOPROTEIN BY PHENOLIC SUBSTANCES IN RED WINE [J].
FRANKEL, EN ;
KANNER, J ;
GERMAN, JB ;
PARKS, E ;
KINSELLA, JE .
LANCET, 1993, 341 (8843) :454-457
[9]   INVERSE CORRELATION BETWEEN PLASMA VITAMIN-E AND MORTALITY FROM ISCHEMIC-HEART-DISEASE IN CROSS-CULTURAL EPIDEMIOLOGY [J].
GEY, KF ;
PUSKA, P ;
JORDAN, P ;
MOSER, UK .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 53 (01) :S326-S334
[10]   GREEN TEA COMPOSITION, CONSUMPTION, AND POLYPHENOL CHEMISTRY [J].
GRAHAM, HN .
PREVENTIVE MEDICINE, 1992, 21 (03) :334-350