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Human Genotoxic Study Carried Out Two Years after Oil Exposure during the Clean-up Activities Using Two Different Biomarkers

机译:使用两种不同的生物标记物在清理活动中的油暴露两年后进行了人类遗传毒性研究

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Micronuclei, comet and chromosome alterations assays are the most widely used biomarkers for determining the genotoxic damage in a population exposed to genotoxic chemicals. While chromosome alterations are an excellent biomarker to detect short- and long-term genotoxic effects, the comet assay only measures early biological effects, and furthermore it is unknown whether nuclear abnormalies, such as those measured in the micronucleus test, remain detectable long-term after an acute exposure. In our previous study, an increase in structural chromosome alterations in fishermen involved in the clean-up of the Prestige oil spill, two years after acute exposure, was detected. The aim of this study is to investigate whether, in lymphocytes from peripheral blood, the nuclear abnormalies (micronucleus, nucleoplasmic bridges and nuclear buds) have a similar sensitivity to the chromosome damage analysis for genotoxic detection two years after oil exposure in the same non-smoker individuals and in the same peripheral blood extraction. No significant differences in nuclear abnormalies frequencies between exposed and non-exposed individuals were found (p 0.05). However, chromosome damage, in the same individuals, was higher in exposed vs. non-exposed individuals, especially for chromosome lesions (p 0.05). These findings, despite the small sample size, suggest that nuclear abnormalities are probably less-successful biomarkers than are chromosome alterations to evaluate genotoxic effects two or more years after an exposure to oil. Due to the great advantage of micronucleus automatic determination, which allows for a rapid study of hundreds of individuals exposed to genotoxic chemical exposure, further studies are needed to confirm whether this assay is or is not useful in long-term genotoxic studies after the toxic agent is no longer present.
机译:微核,彗星和染色体改变测定法是确定暴露于遗传毒性化学物质的人群中遗传毒性损害的最广泛使用的生物标志物。尽管染色体改变是检测短期和长期遗传毒性作用的极佳生物标志物,但彗星试验只能测量早期的生物学作用,此外,核异常(例如在微核试验中测得的核异常)是否仍可长期检测仍是未知的急性暴露后。在我们先前的研究中,发现在急性暴露两年后,参与清理Prestige漏油事件的渔民的结构染色体改变增加了。这项研究的目的是研究在暴露于同一个非脂肪细胞中两年后,外周血淋巴细胞中的核异常(微核,核质桥和核芽)是否对染色体损伤分析的遗传毒性检测具有相似的敏感性。吸烟者与个人在相同的外周血中抽取。暴露者和未暴露者之间的核异常频率无显着差异(p> 0.05)。然而,在同一个体中,染色体损伤在裸露的个体中比未暴露的个体要高,尤其是对于染色体病变(p <0.05)。尽管样本量很小,但这些发现表明,与评估油暴露两年或两年后的遗传毒性影响的染色体改变相比,核异常可能是较不成功的生物标志物。由于微核自动测定的巨大优势,可以快速研究数百名暴露于遗传毒性化学暴露的个体,因此需要进一步的研究,以确认该试验在毒剂后对长期遗传毒性研究中是否有用。不再存在。

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