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Alternative Expression of XRCC1 Gene in Target Organs of Rats Exposed Subchronically to Cadmium

机译:XRCC1基因在亚慢性暴露于镉的大鼠靶器官中的替代表达

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The research is to investigate the alternative expression of XRCC1 gene in target organs of rats exposed subchronically to cadmium (Cd),to understand the toxic effects of certain DNA repair genes in vivo.Based on our pre-established animal model of subchronic cadmium exposure,the abnormal expressions of XRCC1 gene in the liver,kidney,heart and lung of rats treated with CdCl2 at different concentration were detected by fluorescent quantitative polymerase chain reaction (FQ-PCR).The levels of XRCC1 protein were further confirmed by western blotting analysis.Compared to the corresponding controls,under the inner standard of TBP,the expression levels of XRCC1 mRNA were significantly decreased in all the measured liver and kidney in all Cd exposed rats with dose-dependent manner (P<0.01).Among low-dose,mid-dose and high-dose groups of the rats exposed to Cd,FQ-PCR assay showed that the XRCC1 mRNA expressions were respectively 45%,32%,13% of controls in the liver; 68%,31%,16% of controls in the kidney; 42%,30%,15% of controls in the heart; and 47%,28%,19% of controls in the lung.The western blotting analysis further displayed that the tendency of XRCC1 protein level was consistent with XRCC1 mRNA expression,indicating the subchronic Cd exposure cart obviously regulate down the expression of XRCC1 gene in main inner organs of rats.The alternative expression of XRCC1 gene in rat's liver,kidney,heart and lung might be an important biomarker for toxic effects during long-term low level exposure to Cd in vivo.
机译:本研究旨在探讨XRCC1基因在镉(Cd)慢性暴露后靶器官中的替代表达,以了解某些DNA修复基因在体内的毒性作用。基于我们预先建立的亚慢性镉暴露的动物模型,用荧光定量聚合酶链反应(FQ-PCR)检测不同浓度CdCl2处理的大鼠肝,肾,心脏和肺中XRCC1基因的异常表达,并通过western blotting进一步证实XRCC1蛋白的水平。与相应对照组相比,在TBP内标下,所有Cd暴露大鼠肝脏和肾脏中XRCC1 mRNA的表达均呈剂量依赖性降低(P <0.01)。 Cd,FQ-PCR检测大鼠中剂量和高剂量组肝组织中XRCC1 mRNA的表达分别为对照组的45%,32%,13%。肾脏控制68%,31%,16%;心脏控制的42%,30%,15%; Western blotting分析进一步显示XRCC1蛋白水平的变化趋势与XRCC1 mRNA表达相一致,表明亚慢性Cd暴露推车明显下调了XRCC1基因的表达。 XRCC1基因在大鼠肝脏,肾脏,心脏和肺中的交替表达可能是体内长期低水平暴露于Cd期间毒性作用的重要生物标志物。

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