Alkylperoxyl radical-scavenging activity of various flavonoids and other phenolic compounds: Implications for the anti-tumor-promoter effect of vegetables

被引:270
作者
Sawa, T
Nakao, M
Akaike, T
Ono, K
Maeda, H
机构
[1] Kumamoto Univ, Sch Med, Dept Microbiol, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Fac Sci, Dept Biol Sci, Kumamoto 8600862, Japan
关键词
alkylperoxyl radical; flavonoids; phenolic compounds; anti-tumor-promoter; radical scavenger;
D O I
10.1021/jf980765e
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
We recently reported that alkylperoxyl radical (ROO.) enhanced carcinogenesis in rats treated with carcinogen (Sawa et al. Cancer Epidemiol. Biomarkers Prev. 1998, 7, 1007-1012), and the tumor promoting action of ROO. could be reduced by addition of hot-water extracts of vegetables (Maeda et al.;Tpn. J. Cancer Res. 1992, 83, 923-928). Here we described the ROO.-scavenging activity of flavonoids and nonflavonoid phenolics and their role in anti-tumor-promoter effects. A model molecular species, ROO., was generated from tert-butyl hydroperoxide (t-BuOOH) and heme iron, and the scavenging of t-BuOO. was determined by (a) bioassay based on the bactericidal action of ROO., (b) luminol-enhanced chemiluminescence, and (c) electron spin resonance. Of 17 authentic plant phenolics tested, 9 compounds (including rutin, chlorogenic acid, vanillin, vanillic acid, neohesperidin, gallic acid, shikimic acid, rhamnetin, and kaempferol) showed remarkably high ROO.-scavenging activity. Some of them were detected and quantified in hot-water extracts of mung bean sprouts, used as the model vegetable, and their contents increased after germination, which paralleled very well to the ROO.-scavenging capacity of the vegetable extracts. Thus, a diet rich in these radical scavengers would reduce the cancer-promoting action of ROO.. Consequently, the carcinogenic potentials of oxygen-related radicals may be suppressed.
引用
收藏
页码:397 / 402
页数:6
相关论文
共 28 条
[1]   BACTERICIDAL ACTIVITY OF ALKYL PEROXYL RADICALS GENERATED BY HEME-IRON-CATALYZED DECOMPOSITION OF ORGANIC PEROXIDES [J].
AKAIKE, T ;
SATO, K ;
IJIRI, S ;
MIYAMOTO, Y ;
KOHNO, M ;
ANDO, M ;
MAEDA, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 294 (01) :55-63
[2]   DETERMINATION OF PEROXYL RADICAL-SCAVENGING ACTIVITY IN FOOD BY USING BACTERICIDAL ACTION OF ALKYL PEROXYL RADICAL [J].
AKAIKE, T ;
IJIRI, S ;
SATO, K ;
KATSUKI, T ;
MAEDA, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1995, 43 (07) :1864-1870
[3]  
ARUOMA OI, 1989, J BIOL CHEM, V264, P13024
[4]  
BORS W, 1990, METHOD ENZYMOL, V186, P343
[5]   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
[6]   DETECTION OF PEROXYL AND ALKOXYL RADICALS PRODUCED BY REACTION OF HYDROPEROXIDES WITH HEME-PROTEINS BY ELECTRON-SPIN RESONANCE SPECTROSCOPY [J].
DAVIES, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 964 (01) :28-35
[7]   FORMATION OF 8-HYDROXYDEOXYGUANOSINE, HYDROXYL FREE-RADICAL ADDUCT OF DNA IN GRANULOCYTES EXPOSED TO THE TUMOR PROMOTER, TETRADECONYLPHORBOLACETATE [J].
FLOYD, RA ;
WATSON, JJ ;
HARRIS, J ;
WEST, M ;
WONG, PK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 137 (02) :841-846
[8]   HYDROXYL FREE-RADICAL MEDIATED FORMATION OF 8-HYDROXYGUANINE IN ISOLATED DNA [J].
FLOYD, RA ;
WEST, MS ;
ENEFF, KL ;
HOGSETT, WE ;
TINGEY, DT .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1988, 262 (01) :266-272
[9]   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
[10]   OXIDATIVE MECHANISMS IN CARCINOGENESIS [J].
GUYTON, KZ ;
KENSLER, TW .
BRITISH MEDICAL BULLETIN, 1993, 49 (03) :523-544