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首页> 外文期刊>Environmental and molecular mutagenesis. >Pilot studies evaluating the nongenotoxic rodent carcinogens phenobarbital and clofibrate in the rat Pig-a assay
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Pilot studies evaluating the nongenotoxic rodent carcinogens phenobarbital and clofibrate in the rat Pig-a assay

机译:试验研究评估Nongenotoxic啮齿动物癌苯甲虫和氯纤维在大鼠猪 - A测定中

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The Pig-a assay is an emerging and promising in vivo method to determine mutagenic potential of chemicals. Since its development in 2008, remarkable progress has been made in harmonizing and characterizing the test procedures, primarily using known mutagenic chemicals. The purpose of the present study was to evaluate specificity of the Pig-a assay using two nongenotoxic and well-characterized rodent liver carcinogens, phenobarbital and clofibrate, in male F344/DuCrl rats. Daily oral administration of phenobarbital or clofibrate at established hepatotoxic doses for 28 days resulted in substantial hepatic alterations, however, did not increase the frequency of Pig-a mutation markers (RETCD59- and RBCCD59-) compared to vehicle control or pre-exposure (Day -5) mutant frequencies. These results are consistent with the existing literature on the nonmutagenic mode of action (MoA) of phenobarbital and clofibrate liver tumors. The present study contributes to the limited, but expanding evidence on the specificity of the Pig-a assay and further for the investigations of carcinogenic MoAs, i.e., mutagenic or nonmutagenic potential of chemicals. Environ. Mol. Mutagen. 60:42-46, 2019. (c) 2018 Wiley Periodicals, Inc.
机译:猪 - 一种测定是体内方法的出现和有前途,以确定化学品的致突变性潜力。自2008年的发展以来,在主要使用已知的致突化化学物质的协调和表征测试程序方面取得了显着进展。本研究的目的是评估使用两种Nongenotoxic和特征在于特征的啮齿动物肝癌,苯巴比妥和Clofibrate的猪的特异性,在雄性F344 / Ducrl大鼠中。日常口服苯丙酸或Clofibrate在已建立的肝毒性剂量28天导致实质性肝脏改变,但与载体对照或预曝光相比,未增加猪突变标志物(RetCD59-和RBCCD59-)的频率(Day -5)突变频率。这些结果与苯巴罗布拉伯和氯纤维肝肿瘤的非低级作用模式(MOA)的现有文献一致。本研究有助于有限,但扩大了关于猪的特异性的证据 - 一种测定,进一步用于研究致癌MOAs,即致突变性或化学物质的非培养潜力。环境。摩尔。诱惑。 60:42-46,2019。(c)2018 Wiley期刊,Inc。

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