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Influence of different iodinated contrast media on the induction of DNA doublea??strand breaks after in vitro Xa??ray irradiation

机译:不同碘化造影剂对体外Xa射线辐照后DNA双链断裂诱导的影响

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The objective of this work was to examine differences in DNA doublea??strand break induction in peripheral blood lymphocytes after in vitro Xa??ray irradiation between iodinated contrast agents. Four different iodinated Xa??ray contrast agents a?? three of them with two different iodine concentrations a?? and mannitol (negative control; concentration of 150a??mg mannitol per ml blood) were pipetted into blood samples so that there was a concentration of 0, 7.5 or 15a??mg of iodine per ml blood in the samples. Negative controls without contrast medium (0a??mg of iodine per ml blood) were also processed for every irradiation dose. The tubes were exposed to 0, 20 or 500a??mGy in vitro Xa??ray irradiation. After that, the lymphocytes were separated by using densitya??gradient centrifugation. Fluorescence microscopy was applied to determine the average number of ?3H2AXa??foci per lymphocyte in the presence or absence of different contrast media or mannitol. Differences in the number of ?3H2AXa??foci were statistically analysed by onea??way ANOVA and posta??hoc Tukey's honestly significant difference test. Iodinated contrast agents led to a statistically significant increase in DNA doublea??strand breaks after in vitro irradiation. This effect increased statistically significant with rising radiation dose and appeared independent of the contrast agent used (iopromid, iodixanol, iomeprol, iopamidol). A statistically significant difference in DNA damage between the different tested contrast agents was not found. Therefore, the increase in DNA doublea??strand breaks depends solely on the amount of iodine applied. For evaluation of clinical consequences, our findings could be tested in further animal studies. Copyright ?? 2014 John Wiley & Sons, Ltd.
机译:这项工作的目的是检查碘化造影剂在体外Xa射线照射后外周血淋巴细胞DNA双链断裂的诱导差异。四种不同的碘化Xa射线造影剂其中三个具有两个不同的碘浓度将甘露醇和甘露醇(阴性对照;每毫升血液中浓度为150a-3 mg甘露醇)移入血液样品中,以使样品中每毫升血液中的碘浓度为0、7.5或15 a-3 mg。对于每个辐照剂量,也要处理不含造影剂的阴性对照(每毫升血液中0a-10 mg碘)。使试管在体外Xa射线照射下暴露于0、20或500aΔmGy。此后,通过密度梯度离心分离淋巴细胞。在存在或不存在不同的造影剂或甘露糖醇的情况下,用荧光显微术测定每个淋巴细胞的平均β3H2AXaβ位点数。通过单因素方差分析和post-hoc Tukey的真实显着性差异检验统计分析了?3H2AXa?基因位点数目的差异。碘化造影剂在体外照射后导致DNA双链断裂的统计显着增加。随着辐射剂量的增加,这种作用在统计学上显着增加,并且与所使用的造影剂(碘普罗胺,碘克沙醇,碘美普尔,碘帕醇)无关。未发现不同测试造影剂之间DNA损伤的统计学显着差异。因此,DNA双链断裂的增加仅取决于所施加的碘的量。为了评估临床后果,我们的发现可以在进一步的动物研究中进行检验。版权?? 2014 John Wiley&Sons,Ltd.

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