首页|奥克托金对中国仓鼠肺成纤维细胞DNA的氧化应激损伤

奥克托金对中国仓鼠肺成纤维细胞DNA的氧化应激损伤

扫码查看
目的 了解奥克托金(HMX)对中国仓鼠肺成纤维细胞(V79细胞)的细胞毒性及DNA损伤作用.方法 以体外培养V79细胞为研究对象,采用细胞增殖与毒性检测实验方法(CCK-8法)检测5个浓度(5、25、50、75、100 mg/L)HMX溶液染毒24 h对V79细胞的毒性作用;采用单细胞凝胶电泳技术(SCGE)和Elisa方法进行3个浓度(50、75、100 mg/L)HMX溶液染毒24 h后致V79细胞的DNA损伤指标及氧化应激指标.结果 与溶剂对照组比较,50、75、100 mg/L HMX染毒组V79细胞的存活率均降低,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的存活率呈下降趋势.与溶剂对照组相比,50~100 mg/L HMX染毒组V79细胞的尾长、尾部DNA%、尾距和Olive尾距均增加,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的尾长、尾部DNA%、尾距和Olive尾距均呈上升趋势.与溶剂对照组相比,75和100 mg/L的HMX显著增加了 V79细胞的8-OHdG水平,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的8-OHdG水平呈先上升后下降的趋势.与溶剂对照组相比,仅100 mg/L的HMX显著增加了V79细胞的ROS水平,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的ROS水平呈先上升趋势.与溶剂对照组相比,75和100 mg/L的HMX显著增加了 V79细胞的MDA水平,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的MDA水平呈上升趋势.与溶剂对照组相比,各浓度HMX染毒组V79细胞的GSH水平均降低,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的GSH水平呈下降趋势.与溶剂对照组相比,仅75 mg/LHMX染毒组V79细胞的SOD水平降低,差异有统计学意义(P<0.05);且随着HMX染毒浓度的升高,V79细胞的SOD水平呈先下降后升高的趋势.结论 在本实验条件下,HMX能够通过引起细胞氧化损伤诱导细胞毒性,明显抑制V79细胞增殖,导致DNA损伤.
Oxidative stress damage of octogen to DNA in V79 cells
Objective To investigate the cytotoxicity and DNA damage of octogen(HMX)on Chinese hamster lung fibroblasts(V79 cells).Methods Using in vitro cultured V79 cells as the research object,the cell proliferation and toxicity detection experimental method(CCK-8 method)was used to detect the toxic effects of 5 concentrations(5,25,50,75 and 100 mg/L)of HMX solution on V79 cells after 24 hours of exposure;Single cell gel electrophoresis(SCGE)and Elisa method were used to determine the DNA damage index and oxidative stress index of V79 cells exposed to HMX solution at three concentrations(50,75,100 mg/L)for 24 h.Results Compared with the solvent control group,in 50,75,and 100 mg/L groups,the survival rate of V79 cells significantly decreased(P<0.05),and with the increase of HMX concentration,the survival rate of V79 cells showed a decreasing trend.Compared with the solvent control group,in 50-100 mg/L groups,the tail length,tail DNA%,tail distance,and live tail distance of V79 cells significantly increased(P<0.05),and with the increase of HMX concentration,the tail length,tail DNA%,tail distance,and live tail distance of V79 cells all showed an upward trend.Compared to the solvent control group,in 75 and 100 mg/L groups,the 8-OHdG level in V79 cells significantly increased(P<0.05),and with the increase of HMX concentration,the 8-OHdG level of V79 cells showed a trend of first increasing and then decreasing.Compared to the solvent control group,only in 100 mg/L group,the ROS level of V79 cells significantly increased(P<0.05),and with the increase of HMX concentration,the ROS level of V79 cells showed an initial upward trend.Compared to the solvent control group,in 75 and 100 mg/L groups,the MDA level of V79 cells significantly increased(P<0.05),and with the increase of HMX concentration,the MDA level of V79 cells showed an upward trend.Compared with the solvent control group,the GSH levels of V79 cells in the groups treated with HMX at different concentrations decreased significantly(P<0.05),and with the increase of HMX concentration,the GSH level of V79 cells showed a downward trend.Compared to the solvent control group,only in 75 mg/L group,the SOD level of V79 cells significantly decreased(P<0.05),and with the increase of HMX concentration,the SOD level of V79 cells showed a trend of first decreasing and then increasing.Conclusion In the present experiment,HMX can induce cytotoxicity by causing oxidative damage and significantly inhibit V79 cell proliferation,resulting in DNA damage.

Octogen(HMX)V79 cellsOxidative stressDNA damage

邓辉、吕小强、李存治、高婷、李欢、高俊宏

展开 >

兵器工业卫生研究所毒理技术研究中心,陕西西安 710065

西安市毒理与生物效应重点实验室

奥克托金 中国仓鼠肺成纤维细胞 氧化应激 DNA损伤

北京理工大学科研项目

202120929047

2024

环境与健康杂志
中华预防医学会,天津市疾病预防控制中心

环境与健康杂志

CSTPCD
影响因子:0.658
ISSN:1001-5914
年,卷(期):2024.41(3)