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Efficacy of HUMN criteria for scoring the micronucleus assay in human lymphocytes exposed to a low concentration of p,p'-DDT

机译:HUMAN标准对在低浓度p,p'-DDT中暴露的人类淋巴细胞中微核分析进行评分的功效

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The cytokinesis-block micronucleus (CBMN) assay is one of the standard cytogenetic tools employed to assess chromosomal damage subsequent to exposure to genotoxic/cytotoxic agents, and is widely applicable to plant, animal and human cells. In the present study, the CBMN assay was used to assess the baseline damage in binuclear human peripheral blood lymphocytes exposed to 25 μg/L p,p'-DDT for 1, 2, 24, and 48 h by measuring the frequency of micronuclei, nucleoplasmic bridges and nuclear buds. These new scoring criteria facilitated the detection of different types of clastogenic and aneugenic effects induced by this type of pollutant. With these criteria, CBMN can also be used to measure nucleoplasmic bridges which are considered to be consequences of chromosome rearrangements and nuclear buds which are biomarkers of altered gene amplification and gene dosage. The total number of micronuclei observed in binuclear human peripheral blood lymphocytes of the exposed samples (ranging from 32 to 47) was significantly greater (P < 0.05) than that detected in the unexposed (0 time) control sample, where the total number of micronuclei was 7. The number of nucleoplasmic bridges and nuclear buds obtained after 24 and 48 h was also significantly (P < 0.05) greater in the samples treated with p,p'-DDT than in the unexposed control samples. Thus, our results confirmed the usefulness of the new criteria applicable for the CBMN assay employed in measuring the DNA damage and its role of a sensitive cytogenetic biomarker.
机译:胞质分裂阻滞微核(CBMN)分析是用于评估暴露于基因毒性/细胞毒性剂后染色体损伤的标准细胞遗传学工具之一,并且广泛适用于植物,动物和人类细胞。在本研究中,CBMN测定法通过测量微核的频率来评估暴露于25μg/ L p,p'-DDT 1、2、24和48 h的双核人外周血淋巴细胞的基线损伤,核质桥和核芽。这些新的评分标准有助于检测由这种类型的污染物引起的不同类型的致胶剂作用和无气孔作用。有了这些标准,CBMN也可以用于测量核质桥,这被认为是染色体重排和核芽的结果,而核芽是改变基因扩增和基因剂量的生物标记。暴露样品的双核人外周血淋巴细胞中观察到的微核总数(从32到47)显着大于未暴露(0次)对照样品中检测到的微核总数(P <0.05)。 p.p'-DDT处理的样品在24和48 h后获得的核质桥和核芽的数量也显着(P <0.05)比未暴露的对照样品大。因此,我们的结果证实了适用于CBMN测定的新标准的有用性,该测定用于测量DNA损伤及其在敏感的细胞遗传生物标记中的作用。

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