The effect of dietary flavonoids on DNA damage (strand breaks and oxidised pyrimdines) and growth in human cells

被引:154
作者
Duthie, SJ
Johnson, W
Dobson, VL
机构
[1] Rowett Research Institute, Bucksburn, Aberdeen AB21 9SB, Greenburn Road
关键词
comet assay; human cell; flavonoid; genotoxicity; cytotoxicity; diet;
D O I
10.1016/S0165-1218(97)00010-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The effects of the flavonoids quercetin, myricetin and silymarin on DNA damage and cytotoxicity in human cells were investigated. DNA strand breaks and oxidised pyrimidines were determined using alkaline single cell gel electrophoresis (the comet assay). Inhibition of cell growth was also measured. Caco-2 (colon), HepG2 (liver), HeLa (epithelial) cells and normal human lymphocytes showed different, dose-dependent susceptibilities (in terms of strand breakage) to the various flavonoids, quercetin being the most damaging. This agreed well with the ability of the flavonoids to inhibit cell growth. None of the flavonoids induced DNA base oxidation above background levels. All of the flavonoids under investigation caused depletion of reduced glutathione, which, in the case of quercetin, occurred prior to cell death. Neither cytotoxicity nor genotoxicity was associated with the antioxidant enzyme capacity (glutathione, glutathione reductase, glutathione peroxidase and catalase) of the cells.
引用
收藏
页码:141 / 151
页数:11
相关论文
共 57 条
[11]   Antioxidant properties of hydroxy-flavones [J].
Cotelle, N ;
Bernier, JL ;
Catteau, JP ;
Pommery, J ;
Wallet, JC ;
Gaydou, EM .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (01) :35-43
[12]   ISOLATION AND STUDIES OF THE MUTAGENIC ACTIVITY IN THE AMES TEST OF FLAVONOIDS NATURALLY-OCCURRING IN MEDICAL HERBS [J].
CZECZOT, H ;
TUDEK, B ;
KUSZTELAK, J ;
SZYMCZYK, T ;
DOBROWOLSKA, B ;
GLINKOWSKA, G ;
MALINOWSKI, J ;
STRZELECKA, H .
MUTATION RESEARCH, 1990, 240 (03) :209-216
[13]  
DAWSON JR, 1985, BIOCHEM BIOPH RES CO, V143, P52
[15]   ANTIOXIDANT MICRONUTRIENTS IN CANCER PREVENTION [J].
DORGAN, JF ;
SCHATZKIN, A .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1991, 5 (01) :43-68
[16]   STATUS OF REDUCED GLUTATHIONE IN THE HUMAN HEPATOMA-CELL LINE, HEP-G2 [J].
DUTHIE, SJ ;
COLEMAN, CS ;
GRANT, MH .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (17) :3365-3368
[17]   The influence of cell growth, detoxifying enzymes and DNA repair on hydrogen peroxide-mediated DNA damage (measured using the comet assay) in human cells [J].
Duthie, SJ ;
Collins, AR .
FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (04) :717-724
[18]   DRUG TOXICITY MECHANISMS IN HUMAN HEPATOMA HEPG2 CELLS - CYCLOSPORINE-A AND TAMOXIFEN [J].
DUTHIE, SJ ;
MELVIN, WT ;
BURKE, MD .
XENOBIOTICA, 1995, 25 (10) :1151-1164
[19]   THE TOXICITY OF MENADIONE AND MITOZANTRONE IN HUMAN LIVER-DERIVED HEP G2 HEPATOMA-CELLS [J].
DUTHIE, SJ ;
GRANT, MH .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (08) :1247-1255
[20]   INHIBITORY EFFECT OF GRAPEFRUIT JUICE AND ITS BITTER PRINCIPAL, NARINGENIN, ON CYP1A2 DEPENDENT METABOLISM OF CAFFEINE IN MAN [J].
FUHR, U ;
KLITTICH, K ;
STAIB, AH .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 35 (04) :431-436