The effect of flavonoids on ofloxacin-induced mutagenicity in Euglena gracilis

被引:30
作者
Krizková, L
Nagy, M
Polónyi, J
Ebringer, L
机构
[1] Comenius Univ, Inst Mol & Subcellular Biol, Fac Sci, Bratislava, Slovakia
[2] Comenius Univ, Fac Pharm, Dept Phamacognosy & Bot, Bratislava 83232, Slovakia
关键词
Euglena gracilis; flavonoid; antimutagenicity; co-mutagenicity; ofloxacin;
D O I
10.1016/S1383-5718(98)00080-1
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 antimutagenicity of 14 naturally occurring flavonoids (20 mu mol/l) on ofloxacin (43 mu mol/l and 86 mu mol/l)-induced bleaching (mutagenicity) was studied in Euglena gracilis. The flavonoids chrysin, tectochrysin, chrysin-5-methylether, galangin, galangin-5-methylether, pinocembrin and pinobanksin possess considerable antimutagenic properties against ofloxacin-induced bleaching of E. gracilis. Apigenin and isalpinin had only weak antimutagenic potency. Pinobanksin-5-methylether and pinobanksin-3-acetate showed very weak or no antimutagenic effect. However, kempferol, quercetin-3-methylether and quercetin-3,3'-dimethylether showed co-mutagenic or no antimutagenic effect depending on the concentration of ofloxacin. Two possible modes of action of the flavonoids on ofloxacin-induced bleaching of E. gracilis are discussed. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:85 / 92
页数:8
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