Antioxidant activity of various teas against free radicals and LDL oxidation

被引:47
作者
Ohmori, R
Iwamoto, T
Tago, M
Takeo, T
Unno, T
Itakura, H
Kondo, K
机构
[1] Natl Def Med Coll, Dept Internal Med 1, Tokorozawa, Saitama 3598513, Japan
[2] Ochanomizu Univ, Inst Environm Sci Human Life, Bunkyo Ku, Tokyo 1120012, Japan
[3] Itoen Ltd, Ctr Res Inst, Shizuoka 4210516, Japan
[4] Ibaraki Univ, Dept Life Sci, Ibaraki 3191221, Japan
关键词
D O I
10.1007/s11745-005-1447-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tea is a widely consumed beverage throughout the world. We assessed the antioxidant activity of six teas, including the aqueous extracts of green tea and oolong tea (Camellia sinensis), tochu (Eucommia ulmoides), Gymnema sylvestre, Japanese mugwort (Artemisia princeps), and barley (Hordeum vulgare), against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals and LDL oxidation, and examined the association of LDL oxidizability with the plasma catechin levels in 10 healthy volunteers with a single dose of 5 g green tea powder. In vitro, the inhibitory effects of DPPH radicals and LDL oxidation were found to be strongest in the extract of green tea and weakest in that of barley. After the ingestion of green tea powder, the lag time increased from basal 52.2 +/- 4.1 to 60.3 +/- 4.2 min at 1 h and 59.5 +/- 4.1 min at 2 h, and then returned to the baseline lag time (51.9 +/- 1.4 at 4 h and 52.1 +/- 4.7 min at 6 h). Regarding the plasma catechin levels, epigallocatechingallate and epicatechingallate significantly increased from basal 3.7 +/- 1.3 and 0.8 +/- 0.8 ng/mL to 65.7 +/- 11.6 and 54.6 +/- 12.6 ng/mL at 1 h, and 74.4 +/- 18.6 and 49.4 +/- 7.1 ng/mL at 2 h, respectively. Green tea therefore showed the strongest antioxidant activity among the six different teas, and the inhibitory effects of green tea on LDL oxidation depended on the plasma catechin levels.
引用
收藏
页码:849 / 853
页数:5
相关论文
共 33 条
[1]  
[Anonymous], TOB ATL
[2]  
[Anonymous], 1989, WORLD HLTH STAT ANN
[3]   ANTIDIABETIC EFFECT OF A LEAF EXTRACT FROM GYMNEMA-SYLVESTRE IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS PATIENTS [J].
BASKARAN, K ;
AHAMATH, BK ;
SHANMUGASUNDARAM, KR ;
SHANMUGASUNDARAM, ERB .
JOURNAL OF ETHNOPHARMACOLOGY, 1990, 30 (03) :295-305
[4]  
CHUNG BH, 1986, METHOD ENZYMOL, V128, P181
[5]   DOES DIET OR ALCOHOL EXPLAIN THE FRENCH PARADOX [J].
CRIQUI, MH ;
RINGEL, BL .
LANCET, 1994, 344 (8939-4) :1719-1723
[6]  
ESTERBAUER H, 1987, J LIPID RES, V28, P495
[7]   MALONDIALDEHYDE ALTERATION OF LOW-DENSITY LIPOPROTEINS LEADS TO CHOLESTERYL ESTER ACCUMULATION IN HUMAN MONOCYTE-MACROPHAGES [J].
FOGELMAN, AM ;
SHECHTER, I ;
SEAGER, J ;
HOKOM, M ;
CHILD, JS ;
EDWARDS, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (04) :2214-2218
[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]   Sulfated polysaccharide from the leaves of Artemisia princeps activates heparin cofactor II independently of the Lys(173) and Arg(189) residues of heparin cofactor II [J].
Hayashi, T ;
Hayakawa, Y ;
Hayashi, T ;
Sasaki, H ;
Sakuragawa, N .
THROMBOSIS RESEARCH, 1997, 87 (01) :105-112
[10]   DIETARY ANTIOXIDANT FLAVONOIDS AND RISK OF CORONARY HEART-DISEASE - THE ZUTPHEN ELDERLY STUDY [J].
HERTOG, MGL ;
FESKENS, EJM ;
HOLLMAN, PCH ;
KATAN, MB ;
KROMHOUT, D .
LANCET, 1993, 342 (8878) :1007-1011