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DNA damage induced in cells by gamma and UVA radiation as measured by HPLC/GC-MS and HPLC-EC and Comet assay.

机译:HPLC / GC-MS,HPLC-EC和Comet法测定,γ和UVA辐射在细胞中诱导的DNA损伤。

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The aim of the work was to measure DNA damage induced within tumoral human monocytes by gamma rays, UVA radiation, and exogenous photosensitizers. The accurate HPLC-EC assay was used to determine the level of 8-oxodGuo. The formation of FapyGua and FapyAde was monitored by HPLC/GC-MS analyses after formic acid hydrolysis at room temperature. For this purpose, cells were exposed to relatively high doses of gamma rays and UVA radiation. The extent of formation of FapyGua in the DNA of cells exposed to gamma rays was estimated to be more than 2-fold higher than that of 8-oxodGuo, i.e., about 0. 027 lesion per 10(6) bases per Gy. The yield of FapyAde was estimated to be 1 order of magnitude lower. The latter results were used to calibrate the alkaline comet assay associated with DNA N-glycosylases. The latter approach allowed the determination of the background level (0.11-0.16 Fpg-sensitive site/10(6) bases) and the yields of strand breaks and DNA base damage upon low irradiation doses. Insights into the mechanism of radiation-induced DNA damage were gained from these measurements. A major involvement of (1)O(2) with respect to hydroxyl radicals and type I photosensitization was thus observed within cells exposed to UVA radiation.
机译:这项工作的目的是测量伽玛射线,UVA辐射和外源光敏剂在人类肿瘤单核细胞中诱导的DNA损伤。准确的HPLC-EC测定法用于确定8-oxodGuo的水平。室温下甲酸水解后,通过HPLC / GC-MS分析监测FapyGua和FapyAde的形成。为此,将细胞暴露于相对高剂量的伽玛射线和UVA辐射中。据估计,暴露于伽马射线的细胞DNA中FapyGua的形成程度是8-oxodGuo的2倍以上,即每Gy每10(6)个碱基约有0.027处。 FapyAde的产率估计低1个数量级。后一结果用于校准与DNA N-糖基化酶相关的碱性彗星试验。后一种方法可以确定背景水平(0.11-0.16 Fpg敏感位点/ 10(6)碱基)以及低辐照剂量下链断裂和DNA碱基损伤的产量。通过这些测量,可以深入了解辐射诱导的DNA损伤的机制。因此,在暴露于UVA辐射的细胞中观察到(1)O(2)在羟基自由基和I型光敏化方面的主要参与。

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