Cyanidin and cyanidin 3-O-β-D-glucoside as DNA cleavage protectors and antioxidants

被引:137
作者
Acquaviva, R
Russo, A
Galvano, F
Galvano, G
Barcellona, ML
Volti, GL
Vanella, A
机构
[1] Univ Catania, Dept Biochem Med Chem & Mol Biol, Catania, Italy
[2] Univ Catania, Dept Agron Chem & Anim Prod, Catania, Italy
[3] Univ Reggio Calabria, Dept Agroforestry Environm Sci & Technol, I-89100 Reggio Di Calabria, Italy
关键词
anthocyanins; cyanidin; 3-O-beta-D-glucoside; DNA cleavage; free radical; xanthine oxidase;
D O I
10.1023/B:CBTO.0000003974.27349.4e
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Anthocyanins, colored flavonoids, are water-soluble pigments present in the plant kingdom; in fact they are secondary plant metabolites responsible for the blue, purple, and red color of many plant tissues. Present in beans, fruits, vegetables and red wines, considerable amounts of anthocyanins are ingested as constituents of the human diet (180-215 mg daily). There is now increasing interest in the in vivo protective function of natural antioxidants contained in dietary plants against oxidative damage caused by free radical species. Recently, the antioxidant activity of phenolic phytochemicals, has been investigated. Since the antioxidant mechanism of anthocyanin pigments is still controversial, in the present study we evaluated the effects of cyanidin and cyanidin 3-O-beta-D-glucoside on DNA cleavage, on their free radical scavenging capacity and on xanthine oxidase activity. Cyanidin and cyanidin 3-O-beta-D-glucoside showed a protective effect on DNA cleavage, a dose-dependent free radical scavenging activity and significant inhibition of XO activity. These effects suggest that anthocyanins exhibit interesting antioxidant properties, and could therefore represent a promising class of compounds useful in the treatment of pathologies where free radical production plays a key role.
引用
收藏
页码:243 / 252
页数:10
相关论文
共 52 条
[1]  
Bonina F., 1998, International Journal of Cosmetic Science, V20, P331
[2]  
BOWEN PE, 1995, AM J CLIN NUTR, V62, P1403
[3]  
Brouillard R., 1988, The Flavonoids, P525, DOI DOI 10.1007/978-1-4899-2913-6_16
[4]   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
[5]  
CHENG KC, 1992, J BIOL CHEM, V267, P166
[6]   The potential role of iron chelators in the treatment of Parkinson's disease and related neurological disorders [J].
Gassen, M ;
Youdim, MBH .
PHARMACOLOGY & TOXICOLOGY, 1997, 80 (04) :159-166
[7]   Intestinal transport of quercetin glycosides in rats involves both deglycosylation and interaction with the hexose transport pathway [J].
Gee, JM ;
DuPont, MS ;
Day, AJ ;
Plumb, GW ;
Williamson, G ;
Johnson, IT .
JOURNAL OF NUTRITION, 2000, 130 (11) :2765-2771
[8]  
HALLIWELL B, 1990, METHOD ENZYMOL, V186, P1
[9]  
Halliwell Barry, 1993, American Journal of Clinical Nutrition, V57, p715S, DOI 10.1093/ajcn/57.5.715S
[10]  
Harborne J.B., 1988, The Flavonoids, P1, DOI DOI 10.1007/978-1-4899-2913-6_1