首页> 美国卫生研究院文献>Journal of Toxicologic Pathology >Concordance between Results of Medium-term Liver Carcinogenesis Bioassays andLong-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane inF344 Rats
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Concordance between Results of Medium-term Liver Carcinogenesis Bioassays andLong-term Findings for Carcinogenic 2-Nitropropane and Non-carcinogenic 1-Nitropropane inF344 Rats

机译:中期肝癌发生生物测定结果与结果之间的一致性致癌性2-硝基丙烷和非致癌性1-硝基丙烷的长期发现F344大鼠

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摘要

This study was conducted to determine the concordance of results for a pair of structural isomers, 2-nitropropane (2-NP) and 1-nitropropane (1-NP), using the rat medium-term liver carcinogenesis bioassay (Ito test) and previously published long-term carcinogenicity tests. Male F344 rats were given a single intraperitoneal injection of DEN (200 mg/kg b.w.) to initiate hepatocarcinogenesis. After 2 weeks, they received per os 0, 0.8, 4 or 20 mg/kg/day of 2-NP or 1-NP six times a week and were subjected to two-thirds partial hepatectomy at week 3. Non-initiated groups receiving 0 or 20 mg/kg/day were also included. The animals were sacrificed for quantitative analysis of GST-P-positive foci at week 8. With the highest dose of 2-NP, significantly increased numbers and areas of GST-P-positive foci were demonstrated as compared with the respective control but were not noted with 1-NP. In the non-DEN-initiated groups, many small GST-P-positive foci of less than 0.2 mm in diameter were also induced in the rats treated with 2-NP at 20 mg/kg/day but were lacking with 1-NP. These results strongly support that 2-NP is a complete hepatocarcinogen with a potent initiation activity, whereas 1-NP is not.
机译:这项研究是使用大鼠中期肝脏癌变生物测定法(伊藤试验)和以前进行的,以确定一对结构异构体2-硝基丙烷(2-NP)和1-硝基丙烷(1-NP)的结果是否一致。发表了长期致癌性测试。对雄性F344大鼠进行一次腹膜内DEN(200μmg/ kg b.w.)注射,以启动肝癌发生。 2周后,他们每周口服6、0、0.8、4或20μmg/ kg / day的2-NP或1-NP剂量,并在第3周接受三分之二的部分肝切除术。还包括0或20 mg / kg /天。在第8周处死动物以定量分析GST-P阳性灶。与相应的对照组相比,最大剂量的2-NP可显示GST-P阳性灶的数量和面积显着增加,但没有用1-NP表示。在非DEN引发的组中,在以20μg/ kg / day剂量的2-NP处理但缺乏1-NP的大鼠中,也诱发了许多直径小于0.2μmm的小GST-P阳性灶。这些结果强烈支持2-NP是具有有效起始活性的完全肝癌原,而1-NP则不是。

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