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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Cadmium chloride, benzo(a)pyrene and cyclophosphamide tested in the in vitro mammalian cell micronucleus test (MNvit) in the human lymphoblastoid cell line TK6 at Covance laboratories, Harrogate UK in support of OECD draft Test Guideline 487.
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Cadmium chloride, benzo(a)pyrene and cyclophosphamide tested in the in vitro mammalian cell micronucleus test (MNvit) in the human lymphoblastoid cell line TK6 at Covance laboratories, Harrogate UK in support of OECD draft Test Guideline 487.

机译:在Harrogate UK Covance实验室的人淋巴母细胞样细胞系TK6的体外哺乳动物细胞微核试验(MNvit)中测试了氯化镉,苯并(a)and和环磷酰胺,以支持OECD测试草案487。

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摘要

The following genotoxic chemicals were tested in the in vitro micronucleus assay, at Covance Laboratories, Harrogate, UK in the human lymphoblastoid cell line TK6. Cadmium chloride (an inorganic carcinogen), benzo[a]pyrene (a polycyclic aromatic hydrocarbon requiring metabolic activation) and cyclophosphamide (an alkylating agent requiring metabolic activation) were treated with and without cytokinesis block (by addition of cytochalasin B). This work formed part of a collaborative evaluation of the toxicity measures recommended in the draft OECD Test Guideline 487 for the in vitro micronucleus test. The toxicity measures used, capable of detecting both cytostasis and cell death, were relative population doubling, relative increase in cell counts and relative cell counts for treatments in the absence of cytokinesis block, and replication index or cytokinesis blocked proliferation index in the presence of cytokinesis block. All of the chemicals tested gave significant increases in the percentage of micronucleated cells with and without cytokinesis block at concentrations giving approximately 60% toxicity (cytostasis and cell death) or less by all of the toxicity measures used. The outcomes from this series of tests support the use of relative increase in cell counts and relative population doubling, as well as relative cell counts, as appropriate measures of cytotoxicity for the non-cytokinesis blocked in the in vitro micronucleus assay.
机译:在英国哈罗盖特市Covance实验室的体外微核试验中,在人淋巴母细胞系TK6中测试了以下遗传毒性化学物质。氯化镉(一种无机致癌物),苯并[a] py(一种需要代谢活化的多环芳烃)和环磷酰胺(一种需要代谢活化的烷基化剂)在有和没有胞质分裂阻滞的情况下(通过添加细胞松弛素B)进行处理。这项工作是对OECD试验准则487草案中建议的体外微核试验毒性措施进行协作评估的一部分。能够检测细胞停滞和细胞死亡的毒性测定方法是:相对群体增加,在不存在胞质分裂阻滞的情况下治疗的细胞计数和相对细胞数的相对增加,以及在胞质分裂存在的情况下复制指数或胞质分裂阻滞增殖指数块。通过所使用的所有毒性测度,所测试的所有化学物质在具有和不具有胞质分裂阻滞的微核细胞中的百分比均显着增加,其浓度给出的毒性约为60%(细胞停滞和细胞死亡)或更低。该系列测试的结果支持使用细胞计数的相对增加和相对群体加倍,以及相对细胞计数,作为体外微核试验中阻断的非胞质分裂的细胞毒性的适当度量。

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