首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Genotoxic ability of cadmium, chromium and nickel salts studied by kinetochore staining in the cytokinesis-blocked micronucleus assay.
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Genotoxic ability of cadmium, chromium and nickel salts studied by kinetochore staining in the cytokinesis-blocked micronucleus assay.

机译:通过胞嘧啶阻滞微核试验中的线粒体染色研究了镉,铬和镍盐的遗传毒性。

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摘要

The aneugenic and clastogenic ability of cadmium chloride(II), cadmium sulfate(II), nickel chloride(II), nickel sulfate(II), chromium chloride(III) and potassium dichromate(IV) have been evaluated through kinetochore-stained micronucleus test. Traditional genotoxicity assays evaluate DNA damage, gene mutations and chromosome breakage. However, these tests are not adequate to detect aneugenic agents that do not act directly on DNA. Staining kinetochores in the cytokinesis-blocked micronucleus assay is a useful way to discriminate between clastogens and aneuploidogens and may allow a rapid identification of aneuploidy-inducing environmental compounds.Human diploid fibroblasts (MRC-5) were employed. All compounds increased micronuclei frequency in a statistically significant way. However, increases in kinetochore-positive micronuclei frequencies were higher than in kinetochore-negative ones. The present work demonstrates the genotoxic ability of the cadmium and chromium salts studied. Aneugenic as well as clastogenic ability could be observed with this assay. Nickel salts, as it was expected because of their known weak mutagenicity, showed lower genotoxic effects than the other metal salts studied. As the test employed only allows the detection of malsegregation, it is proposed that this mechanism is at least one of those by which the tested metal salts induced aneuploidy. On the other hand, visualization of kinetochores in all experiments suggests that the compounds studied did not act by damaging these structures.
机译:通过线粒体染色的微核试验评估了氯化镉(II),硫酸镉(II),氯化镍(II),硫酸镍(II),氯化铬(III)和重铬酸钾(IV)的气化和裂解能力。 。传统的遗传毒性测定法评估DNA损伤,基因突变和染色体断裂。但是,这些测试不足以检测不直接作用于DNA的气生因子。在胞质分裂阻滞的微核试验中染色动植物是区分clastogens和非整倍体原的有用方法,并且可以快速鉴定诱导非整倍体的环境化合物。使用了人类二倍体成纤维细胞(MRC-5)。所有化合物均以统计学上显着的方式增加了微核频率。但是,线粒体阳性微核频率的增加要高于线粒体阴性微核频率的增加。本工作证明了所研究的镉和铬盐的遗传毒性。用该测定法可以观察到无瘤和无分裂能力。正如人们所期望的那样,由于已知的镍盐弱致突变性,因此镍盐的遗传毒性作用低于其他研究的金属盐。由于所采用的测试仅允许检测出不正确的偏析,因此提出该机理至少是被测金属盐诱导非整倍性的机理之一。另一方面,在所有实验中对动植物的可视化表明所研究的化合物并未通过破坏这些结构发挥作用。

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