Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione induced DNA single strand breaks in Caco-2 cells

被引:148
作者
Aherne, SA [1 ]
O'Brien, NM [1 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Dept Food Sci & Technol, Cork, Ireland
关键词
flavonoids; tert-butylhydroperoxide; menadione; DNA damage; Caco-2; cells; BHT; 1,10-phenanthroline; deferoxamine mesylate; free radicals;
D O I
10.1016/S0891-5849(00)00360-9
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
Protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide (tert-BOOH)- and menadione-induced DNA single strand breaks was investigated in Caco-2 cells. Both tert-BOOH and menadione induced DNA single strand breaks in a concentration-dependent manner. Pre-incubation of Caco-2 cells with either quercetin or rutin for 24 h significantly decreased the formation of DNA single strand breaks evoked by tert-BOOH (P < .05). Iron chelators, 1,10-phenanthroline (o-Phen) and deferoxamine mesylate (DFO), also protected against tert-BOOH-induced DNA damage, whereas butylated hydroxytoluene (BHT) had no effect. Quercetin, and not rutin, decreased the extent of menadione-induced DNA single strand breaks. DFO and BHT, and not o-Phen, protected against menadione-induced DNA strand break formation (P < .05). From the results of this study, iron ions were involved in tert-BOOH-induced DNA single strand break formation in Caco-2 cells, whereas DNA damage evoked by menadione was far more complex. We demonstrated that the flavonoids, quercetin and rutin, protected against tert-BOOH-induced DNA strand breaks by way of their metal ion chelating mechanism. However, quercetin, and not rutin, protected against menadione-induced DNA single strand breaks by acting as both a metal chelator and radical scavenger. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:507 / 514
页数:8
相关论文
共 45 条
[1]   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
[2]   Protection by the flavonoids myricetin, quercetin, and rutin against hydrogen peroxide-induced DNA damage in Caco-2 and Hep G2 cells [J].
Aherne, SA ;
O'Brien, NM .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 34 (02) :160-166
[3]   TERT-BUTYL HYDROPEROXIDE-MEDIATED DNA-BASE DAMAGE IN CULTURED-MAMMALIAN-CELLS [J].
ALTMAN, SA ;
ZASTAWNY, TH ;
RANDERS, L ;
LIN, ZL ;
LUMPKIN, JA ;
REMACLE, J ;
DIZDAROGLU, M ;
RAO, G .
MUTATION RESEARCH, 1994, 306 (01) :35-44
[4]  
[Anonymous], FREE RADICALS BIOL M
[5]   NUTRITION AND HEALTH-ASPECTS OF FREE-RADICALS AND ANTIOXIDANTS [J].
ARUOMA, OI .
FOOD AND CHEMICAL TOXICOLOGY, 1994, 32 (07) :671-683
[6]   OXYGEN RADICALS IN ULCERATIVE-COLITIS [J].
BABBS, CF .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 13 (02) :169-181
[7]   ELABORATION OF CELLULAR DNA BREAKS BY HYDROPEROXIDES [J].
BAKER, MA ;
HE, SQ .
FREE RADICAL BIOLOGY AND MEDICINE, 1991, 11 (06) :563-572
[8]   FRUIT, VEGETABLES, AND CANCER PREVENTION - A REVIEW OF THE EPIDEMIOLOGIC EVIDENCE [J].
BLOCK, G ;
PATTERSON, B ;
SUBAR, A .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1992, 18 (01) :1-29
[9]   OXIDATIVE STRESS BY MENADIONE AFFECTS CELLULAR COPPER AND IRON HOMEOSTASIS [J].
CALDERARO, M ;
MARTINS, EAL ;
MENEGHINI, R .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1993, 126 (01) :17-23
[10]  
COLEMAN JB, 1989, MOL PHARMACOL, V36, P193