首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Genotoxicity of industrial dyes under the inductive effect of ethanol on monooxygenase system in mice.
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Genotoxicity of industrial dyes under the inductive effect of ethanol on monooxygenase system in mice.

机译:在乙醇对小鼠单加氧酶系统的诱导作用下,工业染料的遗传毒性。

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摘要

The genotoxic effects of triarylmethane (Acid Green 16, C.I.44025) and arylmonoazo (Basic Orange 28, developed by Boruta Pigment Plant, Poland, C.I. undisclosed) dyes, were evaluated in Balb/C mice. Animals were fed for 6 days nutritionally adequate Portagen liquid diet (1 kcal/ml) or isocaloric alcoholic diet containing 5% (w/v) ethanol (36% of total calories) in order to induce the cytochrome P-4502E1 monooxygenase. Dye compounds were administered intraperitoneally 30 h before the test at doses: 90 mg/kg of Acid Green 16 and 70 mg/kg of Basic Orange 28. Bone marrow micronucleus test was used for evaluation of genotoxicity of the dyes. Ethanol caused an increase of the level of cytochrome P-450 by 200% and activities of 7-ethoxycoumarin O-deethylase (ECOD) by 650%, 7-ethoxyresorufin O-deethylase (EROD) by 460% and glutathione (GSH)-S-transferase by 60% in the liver. Both dyes exerted genotoxic effect as inferred from a 3-fold increase of frequency of micronucleated polychromatic erythrocytes in bone marrow, and a further increase (2-fold) was caused by ethanol liquid diet combined with Acid Green 16 treatment. Basic Orange 28 genotoxicity remained unaffected by ethanol. It is concluded that: (1) enhancement of genotoxic effect of Acid Green 16 by ethanol is caused by induction of cytochrome P-4502E1 monooxygenases resulting in an increased bioactivation of the dye; (2) lack of enhancement of the genotoxic effect of Basic Orange 28 by ethanol probably results from the dye- and ethanol-mediated stimulation of GSH-S-transferase, bypassing the cytochrome P-4502E1 bioactivation step.
机译:在Balb / C小鼠中评估了三芳基甲烷(Acid Green 16,C.I.44025)和芳基单偶氮(Basic Orange 28,由波兰Boruta Pigment Plant开发,C.I.未公开)染料的遗传毒性作用。给动物饲喂6天的营养充足的Portagen流质饮食(1 kcal / ml)或含有5%(w / v)乙醇(占总卡路里的36%)的等热量酒精饮食,以诱导细胞色素P-4502E1单加氧酶。试验前30小时腹膜内给予染料化合物,剂量为:90 mg / kg的酸性绿16和70 mg / kg的碱性橙28。使用骨髓微核试验评估染料的遗传毒性。乙醇使细胞色素P-450的水平增加200%,使7-乙氧基香豆素O-脱乙基酶(ECOD)的活性增加650%,使7-乙氧基试卤灵O-脱乙基酶(EROD)的活性增加460%,并且使谷胱甘肽(GSH)-S的活性增加-肝脏中60%的转移酶。从骨髓中微核多色红细胞的频率增加3倍可以推断出,两种染料均具有遗传毒性作用,而乙醇流质饮食与Acid Green 16处理相结合则导致进一步的增加(2倍)。碱性橙28的遗传毒性仍然不受乙醇的影响。结论:(1)乙醇增强酸性绿16的遗传毒性作用是由于诱导细胞色素P-4502E1单加氧酶导致染料的生物活化增加所致; (2)乙醇未能增强碱性橙28的遗传毒性作用,可能是由于染料和乙醇介导的GSH-S-转移酶的刺激,绕过了细胞色素P-4502E1的生物激活步骤。

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