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镍冶炼烟尘致NIH/3T3细胞DNA损伤的实验研究
引用本文:吴永会,王军,赵光,于翠平.镍冶炼烟尘致NIH/3T3细胞DNA损伤的实验研究[J].中华劳动卫生职业病杂志,2005,23(5):326-328.
作者姓名:吴永会  王军  赵光  于翠平
作者单位:150086,哈尔滨医科大学公共卫生学院
基金项目:国家自然科学基金资助项目(30371205)
摘    要:目的 研究镍冶炼烟尘致DNA损伤作用.方法 采用单细胞凝胶电泳(SCGE)技术,检测2份镍冶炼烟尘对小鼠NIH/3T3细胞的DNA损伤.结果 相同染毒时间内,随着染毒剂量(除样品2中50.0μg/ml剂量染毒24 h组)加大,细胞拖尾率增高,DNA断裂程度在4 h达到高峰,分别为35.5%、69.7%、85.2%、41.3%、75.7%、89.2%.各受试物在相同剂量下,染毒4 h时均较染毒2 h和染毒24 h细胞拖尾率高.NIH/3T3细胞受到镍冶炼烟尘的受试物作用后,在染毒2 h,样品1、样品2各剂量组的细胞彗星尾DNA含量、尾长(除12.5 μg/ml剂量组外)、尾动差(除样品1的12.5μg/ml剂量组外)均明显高于阴性对照组,差异有统计学意义(P<0.05).在染毒4 h,两样品对细胞DNA的损伤达到高峰,各剂量组的3个指标与对照组的差异有统计学意义(P<0.05).染毒时间延长至24 h,上述3个指标改变程度均较染毒4 h减弱,样品1的彗尾长与对照组的差异无统计学意义(P>0.05).结论 镍冶炼烟尘可不同程度致NIH/3T3细胞DNA损伤.

关 键 词:烟尘  镍冶炼  DNA损伤  彗星试验  NIH/3T3细胞  细胞DNA损伤  镍冶炼烟尘  单细胞凝胶电泳(SCGE)  实验研  染毒时间  DNA损伤作用  染毒剂量  DNA断裂
收稿时间:2005-03-25
修稿时间:2005年3月25日

Experimental study on the DNA damage of NIH/3T3 cells induced by nickel-refining dusts
WU Yong-hui,WANG Jun,ZHAO Guang,YU Cui-ping.Experimental study on the DNA damage of NIH/3T3 cells induced by nickel-refining dusts[J].Chinese Journal of Industrial Hygiene and Occupational Diseases,2005,23(5):326-328.
Authors:WU Yong-hui  WANG Jun  ZHAO Guang  YU Cui-ping
Institution:School of Public Health, Harbin Medical University, Harbin 150086, China
Abstract:OBJECTIVE: To study the effects of nickel-refining dusts on DNA damage in mouse NIH/3T3 cell. METHOD: DNA damage of mouse NIH/3T3 cell induced by two nickel-refining dust samples was determined with single cell gel electrophoresis (SCGE) technique. RESULTS: (1) Under the condition of the same treatment time, the tailed cell (%) of NIH/3T3 cells increased with the increase in doses of nickel-refining dusts (35.5%, 69.7%, 85.2%, 41.3%, 75.7%, 89.2% respectively except for sample 2, 50 microg/ml, 24 h group), and DNA strand breaks reached the peak value at 4 h of exposure; (2) When we treated the NIH/3T3 cells with the same dose of nickel-refining dusts, the tail rate at 4 h was higher than those at 2 h and 24 h of exposure; (3) Both sample 1 and sample 2 with different doses of nickel-refining dusts could induce higher comet tail, DNA%, tail length (except for 12.5 microg/ml), extent of TM (except for sample 1, 12.5 microg/ml) than in control group (P < 0.05). The DNA damage range was significantly increased in different tested doses of nickel-refining dusts and the damage range reached the peak value when the cells were treated for 4 h. CONCLUSION: Nickel-refining dusts could induce different degree DNA damage in NIH/3T3 cells.
Keywords:Dust  nickel refining  DNA damage  Comet assay
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