Guzmán Rincón J, Espinosa J, Graf U
Institute of Toxicology, Swiss Federal Institute of Technology (ETH) and University of Zurich, Schwerzenbach.
Mutat Res. 1998 Jan 13;412(1):69-81. doi: 10.1016/s1383-5718(97)00174-5.
The in vivo nitrosation capacity of third-instar larvae of Drosophila melanogaster was assessed using the wing somatic mutation and recombination test (SMART). Larvate derived from two different crosses, the standard cross (ST) and the high bioactivation cross (HB) both involving the recessive wing cell markers multiple wing hairs (mwh) and flare (flr3), were used. The HB cross is characterised by an increased cytochrome P450-dependent bioactivation capacity for promutagens and procarcinogens. The larvae were treated either with methyl urea, sodium nitrite or its combination. N-Nitrosomethylurea was used as a positive control. The wings of the resulting flies were analysed for the occurrence of mutant spots produced by various types of mutational events or by mitotic recombination. Methyl urea is negative in the ST and the HB cross, whereas sodium nitrite is weakly genotoxic in both crosses. However, the combination of both compounds produces highly increased frequencies of mutations and recombinations predominantly in the HB cross. The genotoxic effects produced by the combined treatments were considerably increased when mashed potatoes or an agar-yeast medium were used for the treatment instead of the standard instant medium. Treatment of larvae with the mixture resulting from the in vitro reaction of nitrosation precursors also resulted in high frequencies of induced spots comparable to those recorded with the potent genotoxin N-nitrosomethylurea. Further experiments showed that the genotoxic effect resulting from the in vivo exposure to nitrosation precursors can be reduced by co-treatment with catechin, a known nitrosation inhibitor. The present study demonstrates that the wing spot test is well suited for the determination of genotoxicity produced by in vivo nitrosation processes and for the study of their modulation by individual compounds or dietary complex mixtures.
利用翅体细胞突变和重组试验(SMART)评估了黑腹果蝇三龄幼虫的体内亚硝化能力。使用了来自两个不同杂交组合的幼虫,即标准杂交组合(ST)和高生物活化杂交组合(HB),这两个组合都涉及隐性翅细胞标记多翅毛(mwh)和耀斑(flr3)。HB杂交组合的特征是对前诱变剂和前致癌物的细胞色素P450依赖性生物活化能力增强。幼虫分别用甲基脲、亚硝酸钠或其组合进行处理。N-亚硝基甲基脲用作阳性对照。分析所得果蝇的翅膀,以确定由各种类型的突变事件或有丝分裂重组产生的突变斑的出现情况。甲基脲在ST和HB杂交组合中呈阴性,而亚硝酸钠在两个杂交组合中均具有弱遗传毒性。然而,两种化合物的组合主要在HB杂交组合中产生了高度增加的突变和重组频率。当使用土豆泥或琼脂酵母培养基代替标准速溶培养基进行处理时,联合处理产生的遗传毒性效应显著增加。用亚硝化前体的体外反应产生的混合物处理幼虫也导致了与用强效基因毒素N-亚硝基甲基脲记录的频率相当的高诱导斑频率。进一步的实验表明,可以通过与已知亚硝化抑制剂儿茶素共同处理来降低体内暴露于亚硝化前体所产生的遗传毒性效应。本研究表明翅斑试验非常适合于测定体内亚硝化过程产生的遗传毒性,以及研究其受单个化合物或膳食复杂混合物调节的情况。