No effect of consumption of green and black tea on plasma lipid and antioxidant levels and on LDL oxidation in smokers

被引:145
作者
Princen, HMG
van Duyvenvoorde, W
Buytenhek, R
Blonk, C
Tijburg, LBM
Langius, JAE
Meinders, AE
Pijl, H
机构
[1] TNO, PG, Gaubius Lab, NL-2301 CE Leiden, Netherlands
[2] Unilever Res Labs Vlaardingen, NL-3130 AC Vlaardingen, Netherlands
[3] Univ Leiden Hosp, Dept Dietet, NL-2300 RC Leiden, Netherlands
[4] Univ Leiden Hosp, Dept Gen Internal Med, NL-2300 RC Leiden, Netherlands
关键词
tea; flavonoids; antioxidants; LDL oxidation; plasma cholesterol;
D O I
10.1161/01.ATV.18.5.833
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Intake of flavonoids is associated with a reduced cardiovascular risk. Oxidation of LDL is a major step in atherogenesis, and antioxidants may protect LDL from oxidation. Because tea is an important source of flavonoids, which are strong antioxidants, we have assessed in a randomized, placebo-controlled study the effect of consumption of black and green tea and of intake of isolated green tea polyphenols on LDL oxidation ex vivo and on plasma levels of antioxidants and lipids. Healthy male and female smokers (aged 34+/-12 years, 13 to 16 per group) consumed during a 4-week period 6 cups (900 mL) of black or green tea or water per day, or they received as a supplement 3.6 grams of green tea polyphenols per day (equivalent to the consumption of 18 cups of green tea per day). Consumption of black or green tea had no effect on plasma cholesterol and triglycerides, HDL and LDL cholesterol, plasma vitamins C and E, beta-carotene, and uric acid. No differences were found in parameters of LDL oxidation. Intake of green tea polyphenols decreased plasma vitamin E significantly in that group compared with the control group (-11% P=.016) but had no effect on LDL oxidation ex vivo. We conclude that consumption of black or green tea (6 cups per day) has no effect on plasma lipids and no sparing effect on plasma antioxidant vitamins and that intake of a high dose of isolated green tea polyphenols decreases plasma vitamin E. Although tea polyphenols had a potent antioxidant activity on LDL oxidation in vitro, no effect was found on LDL oxidation ex vivo after consumption of green or black tea or intake of a green tea polyphenol isolate.
引用
收藏
页码:833 / 841
页数:9
相关论文
共 68 条
[1]  
Alpha-Tocopherol Beta Carotene Cancer Prevention Study Group, 1994, N Engl J Med, V330, P1029, DOI 10.1056/NEJM199404143301501
[2]   EFFECTS OF COFFEE AND TEA ON LIPOPROTEINS AND PROSTANOIDS [J].
ARO, A ;
KOSTIAINEN, E ;
HUTTUNEN, JK ;
SEPPALA, E ;
VAPAATALO, H .
ATHEROSCLEROSIS, 1985, 57 (01) :123-128
[3]  
Balentine D. A., 1992, PHENOLIC COMPOUNDS F, V506, P102
[4]   POSITIONAL DISTRIBUTION OF STEARIC-ACID AND OLEIC-ACID IN A TRIACYLGLYCEROL AND DIETARY CALCIUM-CONCENTRATION DETERMINES THE APPARENT ABSORPTION OF THESE FATTY-ACIDS IN RATS [J].
BRINK, EJ ;
HADDEMAN, E ;
DEFOUW, NJ ;
WESTSTRATE, JA .
JOURNAL OF NUTRITION, 1995, 125 (09) :2379-2387
[5]   Effect of 17 beta-estradiol on plasma lipids and LDL oxidation in postmenopausal women with type II diabetes mellitus [J].
Brussaard, HE ;
Leuven, JAG ;
Kluft, C ;
Krans, HMJ ;
vanDuyvenvoorde, W ;
Buytenhek, R ;
vanderLaarse, A ;
Princen, HMG .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (02) :324-330
[6]  
CHOW CK, 1986, J AM COLL NUTR, V5, P305
[7]   FREE-RADICAL CHEMISTRY OF CIGARETTE-SMOKE AND ITS TOXICOLOGICAL IMPLICATIONS [J].
CHURCH, DF ;
PRYOR, WA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1985, 64 :111-126
[8]  
Clifton Peter M., 1995, Current Opinion in Lipidology, V6, P20, DOI 10.1097/00041433-199502000-00005
[9]   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
[10]   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