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The in vivo rat micronucleus test: integration with a 14-day study.

机译:体内大鼠微核试验:与一项为期14天的研究相结合。

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摘要

A 14-day subchronic toxicity study is routinely conducted in Fischer 344 rats at the Lilly Research Laboratories. This study is done to gather preliminary toxicological information about chemical entities showing efficacy in various pharmacological screens. This manuscript describes the validation of a method for evaluating micronuclei in the bone marrow polychromatic erythrocytes of animals from this test in order to obtain additional information about the genotoxic potential of these compounds without incurring the cost of additional animals or the use of additional test article, which is often in limited supply. Compounds selected for evaluation were acetylsalicylic acid, mitomycin C, cyclophosphamide, colchicine, 6-mercaptopurine, and etoposide. With the exception of colchicine, the results obtained were as expected with acetylsalicylic acid yielding negative results and the other compounds yielding positive results. These findings are consistent with those published for mice (MacGregor et al., Fund. Appl. Toxicol., 14, 513-522, 1990) and show that a bone marrow micronucleus test can be successfully integrated into a routine subchronic rat toxicology study.
机译:礼来研究实验室通常在Fischer 344大鼠中进行为期14天的亚慢性毒性研究。进行这项研究是为了收集有关化学实体的初步毒理学信息,这些信息在各种药理学筛选中均显示功效。这份手稿描述了一项用于评估该试验动物骨髓多色红细胞中微核的方法的验证,以便获得有关这些化合物遗传毒性潜力的其他信息,而又不会增加其他动物的成本或使用其他试验物品的费用,通常供应有限。选择进行评估的化合物是乙酰水杨酸,丝裂霉素C,环磷酰胺,秋水仙碱,6-巯基嘌呤和依托泊苷。除秋水仙碱外,所获得的结果均与预期一致,乙酰水杨酸产生阴性结果,其他化合物产生阳性结果。这些发现与针对小鼠发表的那些发现是一致的(MacGregor等,Fund.Appl.Toxicol。,14,513-522,1990),并表明骨髓微核试验可以成功地整合到常规的亚慢性大鼠毒理学研究中。

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