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在大鼠Pig-a试验中评估非遗传毒性啮齿动物致癌物苯巴比妥和氯贝丁酯的初步研究。

Pilot studies evaluating the nongenotoxic rodent carcinogens phenobarbital and clofibrate in the rat Pig-a assay.

作者信息

Ji Zhiying, Settivari Raja S, LeBaron Matthew J

机构信息

Toxicology and Environmental Research and Consulting, The Dow Chemical Company, Midland, Michigan.

出版信息

Environ Mol Mutagen. 2019 Jan;60(1):42-46. doi: 10.1002/em.22232. Epub 2018 Oct 19.

Abstract

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 (RET and RBC ) 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. © 2018 Wiley Periodicals, Inc.

摘要

Pig-a试验是一种新兴且有前景的体内方法,用于确定化学物质的诱变潜力。自2008年开发以来,在协调和表征测试程序方面取得了显著进展,主要使用已知的诱变化学物质。本研究的目的是在雄性F344/DuCrl大鼠中,使用两种非遗传毒性且特征明确的啮齿动物肝脏致癌物苯巴比妥和氯贝丁酯,评估Pig-a试验的特异性。以既定的肝毒性剂量每日口服苯巴比妥或氯贝丁酯28天,导致了显著的肝脏改变,然而,与溶剂对照组或预暴露(第-5天)的突变频率相比,并未增加Pig-a突变标记(RET和RBC)的频率。这些结果与关于苯巴比妥和氯贝丁酯肝肿瘤非诱变作用模式(MoA)的现有文献一致。本研究为关于Pig-a试验特异性的有限但不断增加的证据做出了贡献,并进一步为致癌作用模式的研究,即化学物质的诱变或非诱变潜力的研究做出了贡献。《环境与分子突变》60:42 - 46,2019年。© 2018威利期刊公司

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