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首页> 外文期刊>Genes and environment >Evaluation of the Genotoxicity of Aristolochic Acid in the Kidney and Liver of F344 gpt delta Transgenic Rat Using a 28-Day Repeated-dose Protocol: A Collaborative Study of the gpt delta Transgenic Rat Mutation Assay
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Evaluation of the Genotoxicity of Aristolochic Acid in the Kidney and Liver of F344 gpt delta Transgenic Rat Using a 28-Day Repeated-dose Protocol: A Collaborative Study of the gpt delta Transgenic Rat Mutation Assay

机译:使用28天重复剂量方案评估马兜铃酸对F344 gpt三角洲转基因大鼠肾脏和肝脏的遗传毒性:gpt三角洲转基因大鼠突变检测的合作研究

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摘要

Transgenic rat gene-mutation assays can be used to assess genotoxicity of chemicals in target organs for carcinogenicity. Since gene mutations in transgenes are genetically neutral and thus accumulate along with treatment periods, the assays are suitable for genotoxicity risk assessment of chemicals using repeated-dose treatment methodologies. However, few studies have been conducted to examine the suitability of the assays in repeat-dose treatment protocols. In order to prove the utility of the transgenic rat assays, we treated gpt delta rats with aristolochic acid at 0.3 and 1 mg/kg by gavage daily for 28 days, and autopsied the rats 3 days after the ?nal treatment, which is a protocol recommended by the International Workshop on Genotoxicity Testing (IWGT). Aristolochic acid exists in herbs and some other plants, and is carcinogenic in the kidney, bladder and stomach in rats. The mutant frequency (MF) in both the kidney and the liver increased signi?cantly in a dose-dependent manner when the rats were treated with aristolochic acid.We concluded that the gpt delta rat assay is sensitive enough to detect gene mutations induced by aristolochic acid and also that the 28-day repeated-dose protocol is suitable for assessing genotoxicity of chemicals.
机译:转基因大鼠基因突变检测可用于评估靶器官中化学物质的致癌性。由于转基因中的基因突变在遗传上是中性的,因此随着治疗时间的推移而积累,因此该测定适用于使用重复剂量治疗方法进行化学物质的遗传毒性风险评估。但是,很少有研究检查重复剂量治疗方案中该方法的适用性。为了证明转基因大鼠实验的实用性,我们每天用管饲法以0.3和1 mg / kg的马兜铃酸处理gpt delta大鼠28天,并在最终治疗后3天对大鼠进行解剖。由国际基因毒性测试讲习班(IWGT)推荐。马兜铃酸存在于草药和其他一些植物中,并且在大鼠的肾脏,膀胱和胃中具有致癌性。当用马兜铃酸治疗大鼠时,肾脏和肝脏中的突变频率(MF)均呈剂量依赖性显着增加。我们得出结论,gpt delta大鼠测定足以检测由马兜铃酸诱导的基因突变酸,以及28天重复剂量方案适合评估化学品的遗传毒性。

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