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Oxidative changes and apoptosis induced by 1800-MHz electromagnetic radiation in NIH/3T3 cells

机译:1800 MHz电磁辐射诱导NIH / 3T3细胞的氧化变化和凋亡

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To investigate the potential adverse effects of mobile phone radiation, we studied reactive oxygen species (ROS), DNA damage and apoptosis in mouse embryonic fibroblasts (NIH/3T3) after intermittent exposure (5 min on/10 min off, for various durations from 0.5 to 8 h) to an 1800-MHz GSM-talk mode electromagnetic radiation (EMR) at an average specific absorption rate of 2 W/kg. A 2',7'-dichlorofluorescin diacetate fluorescence probe was used to detect intracellular ROS levels, immunofluorescence was used to detect gamma H2AX foci as a marker for DNA damage, and flow cytometry was used to measure apoptosis. Our results showed a significant increase in intracellular ROS levels after EMR exposure and it reached the highest level at an exposure time of 1 h (p < 0.05) followed by a slight decrease when the exposure continued for as long as 8 h. No significant effect on the number of gamma H2AX was detected after EMR exposure. The percentage of late-apoptotic cells in the EMR-exposed group was significantly higher than that in the sham-exposed groups (p < 0.05). These results indicate that an 1800-MHz EMR enhances ROS formation and promotes apoptosis in NIH/3T3 cells.
机译:为了研究手机辐射的潜在不利影响,我们研究了间歇性暴露(5分钟开启/ 10分钟关闭,从0.5开始的不同时间)后小鼠胚胎成纤维细胞(NIH / 3T3)中的活性氧(ROS),DNA损伤和凋亡至8 h)的平均比吸收率为2 W / kg的1800-MHz GSM通话模式电磁辐射(EMR)。使用2',7'-二氯荧光素二乙酸酯荧光探针检测细胞内ROS水平,使用免疫荧光检测作为DNA损伤标记物的γH2AX病灶,并使用流式细胞仪检测细胞凋亡。我们的结果显示,EMR暴露后细胞内ROS水平显着增加,并且在1 h的暴露时间达到最高水平(p <0.05),然后在长达8 h的暴露时间下略有下降。 EMR暴露后未检测到对H2AX数量的显着影响。暴露于EMR的组中晚期凋亡细胞的百分比显着高于假暴露组(p <0.05)。这些结果表明,1800-MHz EMR增强了NIH / 3T3细胞中的ROS形成并促进了细胞凋亡。

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