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评价幼龄大鼠肝脏微核试验(四):合作研究组进行的微核试验(CSGMT)/日本环境诱变剂学会(JEMS)-哺乳动物诱变性研究组(MMS)的双剂量/单取样法研究。

Evaluation of a liver micronucleus assay in young rats (IV): a study using a double-dosing/single-sampling method by the Collaborative Study Group for the Micronucleus Test (CSGMT)/Japanese Environmental Mutagen Society (JEMS)-Mammalian Mutagenicity Study Group (MMS).

机构信息

Mitsubishi Chemical Medience Corporation, 14 Sunayama, Kamisu-shi, Ibaraki 314-0255, Japan.

出版信息

Mutat Res. 2010 Apr 30;698(1-2):24-9. doi: 10.1016/j.mrgentox.2010.02.010. Epub 2010 Feb 25.

Abstract

A collaborative study was conducted to evaluate whether a liver micronucleus assay using four-week-old male F344 rats can be used to detect genotoxic rat hepatocarcinogens using double-dosing with a single-sampling 4 days after the second dose. The assay methods were thoroughly validated by the seven laboratories involved in the study. Seven chemicals, 2,4-diaminotoluene, diethyl nitrosamine, p-dimethylaminoazobenzene, 1,2-dimethylhydrazine dihydrochloride, 2,4-dinitrotolunene, 2,6-dinitrotoluene and mitomycin C, known to produce positive responses in the single-dosing/triple-sampling method were selected for use in the present study, and each chemical was examined in two laboratories with the exception of 2,4-dinitrotolunene. Although several of the compounds were examined at lower doses for reasons of toxicity than in the single-dosing/triple-sampling method, all chemicals tested in the present study induced micronuclei in liver cells indicating a positive result. These findings suggest that the liver micronucleus assay can be used in young rats to detect genotoxic rat hepatocarcinogens using a double-dosing/single-sampling procedure. Further, the number of animals used in the liver micronucleus assay can be reduced by one-third to a half by using the double-dosing/single-sampling method. This reduction in animal numbers also has significant savings in time and resource for liver perfusion and hepatocyte isolation.

摘要

采用双剂量一次取样法,在第二次给药后 4 天进行检测,以评估使用四周龄雄性 F344 大鼠进行肝脏微核试验是否可以检测遗传毒性大鼠肝致癌物。本研究涉及的七个实验室对该检测方法进行了全面验证。选择了 7 种已知在单次给药/三次取样方法中产生阳性反应的化学物质,2,4-二氨基甲苯、二乙基亚硝胺、对二甲氨基偶氮苯、1,2-二甲基肼二盐酸盐、2,4-二硝基甲苯、2,6-二硝基甲苯和丝裂霉素 C,用于本研究,除了 2,4-二硝基甲苯之外,每种化学物质都在两个实验室进行了检查。尽管由于毒性原因,某些化合物的剂量比单次给药/三次取样方法低,但本研究中测试的所有化学物质均诱导了肝细胞中的微核,表明结果为阳性。这些发现表明,肝脏微核试验可以用于年轻大鼠,通过双剂量一次取样程序检测遗传毒性大鼠肝致癌物。此外,通过双剂量一次取样法,可以将肝脏微核试验中使用的动物数量减少三分之一至一半。这种动物数量的减少也显著节省了肝脏灌注和肝细胞分离的时间和资源。

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