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涂白杰, 彭斌. 苯并[a]芘染毒致小鼠脑组织胞核DNA损伤[J]. 中国公共卫生, 2006, 22(1): 82-83. DOI: 10.11847/zgggws2006-22-01-43
引用本文: 涂白杰, 彭斌. 苯并[a]芘染毒致小鼠脑组织胞核DNA损伤[J]. 中国公共卫生, 2006, 22(1): 82-83. DOI: 10.11847/zgggws2006-22-01-43
TU Baijie, PENG Bin.. Brain tissue DNA damage in benzo[a]pyrene-poisoned mice[J]. Chinese Journal of Public Health, 2006, 22(1): 82-83. DOI: 10.11847/zgggws2006-22-01-43
Citation: TU Baijie, PENG Bin.. Brain tissue DNA damage in benzo[a]pyrene-poisoned mice[J]. Chinese Journal of Public Health, 2006, 22(1): 82-83. DOI: 10.11847/zgggws2006-22-01-43

苯并a芘染毒致小鼠脑组织胞核DNA损伤

Brain tissue DNA damage in benzoapyrene-poisoned mice

  • 摘要:
      目的   研究苯并a芘(BaP)染毒对小鼠脑组织胞核DNA的损伤.
      方法   将50只昆明种小鼠随机分为5组, 每组10只, 染毒组分为高、中、低3个剂量组, 并设溶剂对照及空白对照组.染毒组用BaP的植物油溶剂进行腹腔注射处理, 高、中、低剂量组每次分别腹腔注射BaP 7.8, 3.2和1.3 mg/kg, 每周4次.溶剂对照组用植物油溶剂作平行处理, 空白对照组不做处理.实验中观察记录小鼠一般情况及神经系统症状, 染毒10周后取各组小鼠脑组织制作切片及细胞悬液, DNA断点末端核糖核酸转移酶地高辛标记法(TUNEL)及单细胞凝胶电泳(SCGE)2种方法检测小鼠脑组织神经细胞DNA的损伤.
      结果   (1) 高剂量BaP染毒组小鼠有明显的全身及神经系统中毒症状.(2)TUNEL法检测, 染毒组与对照组以及不同剂量BaP染毒组之间小鼠脑组织胞核DNA损伤率差异均有统计学意义(P < 10 -16~10 -62).(3)SCGE法检测, 高剂量BaP染毒组与对照组之间小鼠脑组织胞核DNA损伤程度差异有统计学意义(P < 0.05).
      结论   高剂量BaP具有神经系统毒性.BaP染毒可引起小鼠脑组织胞核DNA损伤, 损伤率及损伤程度随染毒剂量增加而增加.

     

    Abstract:
      Objective   To study the DNA damage of benzoapyrene on mice br ain t issue.
      Methods   50 mice were divided into 5 groups randomly, there were 10 animals in each g roup:1control group; ovehicle group; low dose BaP group; ¼ medium dose BaP group; ½ high dose BaP group.The mice of low, medium and high dose BaP groups were administrated by intraperitoneal injection wit h BaP dissolved in vegetable oil at 1.3mg/kg, 3.2mg/kg and 7.8 mg/kg once, 4 times per week specially, the vehicle control group were given vegetable oil parallel and the control group were not given additional treatment.Some tox icological symptomes were observed during the experiments.After 10 weeks expose the mice were killed, the brains were removed.The DNA damage of t he mice brain tissues were detected by the methods of TdT-mediated xdUT P nick end Lableing(TU NEL)and Single Cell Glue Electrophor esis(SCGE).
      Results   1There were some neuro-toxic symptoms had been observed in BaP exposed mice, especial in the high-dose BaP group.oBy the method of TUEL, there were very significant differences of the damage rates between administrated g roups and control groups; there w er e very significant differences of the damag e rates among the low, medium and high dose BaP administrated groups(P < 10 -16~10 -62).By the method of SCGE, there were significant differences of DNA damage betw een the high dose BaP administrated group and the control groups(P < 0.05).
      Conclusion   Administration of BaP could damageneuron DNA of the mice brain, the high the BaP administration doses were, the high the damage rates were and the serious the DNA damage was.

     

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