首页> 外文期刊>Collection of Czechoslovak Chemical Communications >~(32)P-Postlabelling Analysis of Dna Adducts with 1-(Phenylazo)-2-Naphthol (Sudan I, Solvent Yellow 14) Formed in vivo In Fisher 344 Rats
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~(32)P-Postlabelling Analysis of Dna Adducts with 1-(Phenylazo)-2-Naphthol (Sudan I, Solvent Yellow 14) Formed in vivo In Fisher 344 Rats

机译:在Fisher 344大鼠体内形成的1-(苯基偶氮)-2-萘酚(苏丹I,溶剂黄14)对Dna加合物的〜(32)P后标记分析

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We report the analysis of DNA adducts with 1-(phenylazo)-2-naphthol in the liver and urinary bladder of Fisher 344 rats treated orally with this dye. DNA adducts were detected and quantitated using the nuclease P1-enhanced version of the ~(32)P-postlabelling assay. Two variations of multidirectional chromatographic systems were used to resolve either bulky and/or smaller (polar) ~(32)P-labelled adducts by TLC. In the present study, a double oral administration of the dye (500 mg/kg) for one day yielded negative results in ~(32)P-postlabelling assay of liver DNA (24 h after dosing). However, three DNA adducts in the urinary bladder were detected under the same conditions of treatment. Chromatography experiments indicated that the two principal DNA adducts detected in the urinary bladder of Fisher 344 rats were the same as those detected in DNA modified by 1-(phenylazo)-2-naphthol and its metabolite 1-(phenylazo)naphthalene-2,6-diol after their activation with peroxidase in vitro. The results presented here strongly suggest that peroxidase itself or in a combination with cytochrome P450 participates in the initiation phase of 1-(phenylazo)-2-naphthol carcinogenesis in the urinary bladder.
机译:我们报告了用该染料口服治疗的Fisher 344大鼠肝脏和膀胱中1-(苯基偶氮)-2-萘酚与DNA加合物的分析。使用〜(32)P后标记测定的核酸酶P1增强版检测并定量DNA加合物。多向色谱系统的两种变体用于通过TLC拆分体积较大和/或较小的(极性)〜(32)P标记的加合物。在本研究中,一天两次口服染料(500 mg / kg)在肝脏DNA的〜(32)P后标记测定(给药后24小时)中产生阴性结果。然而,在相同的治疗条件下,在膀胱中检测到三个DNA加合物。色谱实验表明,在Fisher 344大鼠膀胱中检测到的两个主要DNA加合物与在1-(苯基偶氮)-2-萘酚及其代谢产物1-(苯基偶氮)萘-2,6修饰的DNA中检测到的相同。 -二醇在体外被过氧化物酶激活后。这里给出的结果有力地表明,过氧化物酶本身或与细胞色素P450的组合参与了膀胱中1-(苯基偶氮)-2-萘酚致癌作用的起始阶段。

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