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项华, 潘尽草, 章晓玲, 寇宇, 查捷, 俞国强, 王衡. 铅对妊娠期及新生期大鼠神经细胞DNA的损伤[J]. 中国公共卫生, 2005, 21(7): 829-830. DOI: 10.11847/zgggws2005-21-07-33
引用本文: 项华, 潘尽草, 章晓玲, 寇宇, 查捷, 俞国强, 王衡. 铅对妊娠期及新生期大鼠神经细胞DNA的损伤[J]. 中国公共卫生, 2005, 21(7): 829-830. DOI: 10.11847/zgggws2005-21-07-33
XIANG Hua, PAN Jincao, ZHANG Xiaoling, . Study on DNA damage of neural cells during pregnancy and newborn in lead-induced rats[J]. Chinese Journal of Public Health, 2005, 21(7): 829-830. DOI: 10.11847/zgggws2005-21-07-33
Citation: XIANG Hua, PAN Jincao, ZHANG Xiaoling, . Study on DNA damage of neural cells during pregnancy and newborn in lead-induced rats[J]. Chinese Journal of Public Health, 2005, 21(7): 829-830. DOI: 10.11847/zgggws2005-21-07-33

铅对妊娠期及新生期大鼠神经细胞DNA的损伤

Study on DNA damage of neural cells during pregnancy and newborn in lead-induced rats

  • 摘要:
      目的   研究妊娠期及新生期母体铅暴露对新生仔鼠神经细胞DNA损伤作用, 以进一步揭示铅的神经毒性作用机制。
      方法   SD孕鼠随机分为6组, 妊娠第1d至新生仔鼠出生后第28d进行醋酸铅Pb(CH3COOH)20, 50, 80, 120, 200mg/(kg·bw)连续经口灌胃染毒。取出生8d的新生仔鼠的海马和皮层细胞, 进行单细胞分离后, 采用单细胞凝胶电泳(彗星试验)检测细胞, 观察DNA迁移长度及拖尾细胞百分率。
      结果   各剂量醋酸铅均可引起神经细胞DNA的单链断裂, 出现彗星拖尾, 其拖尾细胞百分率DNA迁移长度均随醋酸铅剂量的增加而增长, 各剂量与阴性对照的结果比较均差异有统计学意义(P < 0.05)。
      结论   醋酸铅可引起神经细胞DNA损伤, 并与剂量呈正相关; 单细胞凝胶电泳是检测神经细胞遗传毒性及细胞凋亡的有效方法。

     

    Abstract:
      Objective   To study the effect of lead exposure during pregnancy and new born on DNA damage in the neural cells of newborn rat.
      Methods   Pregnant rats were divided into six groups randomly, and were treated with lead acetate at the dosage of 0, 50, 80, 120, 150, 200 mg/(kg·bw)by gastric feeding from day 1 of gestation to day 8 after delivery.The single cells were dissociated from hippo camous and cerbral cortex of new born rats at 8 days old.Then single cell gel electrophoresis test was used to measure the DNA damage.Comet length means and percentage of tailed cell were observed.
      Results   The lead acetate could induce the breakage of DNA single strand and resulted in comet cells with tail in every treatment dosage groups compared with control group(P < 0.05).Both the number of comet cells and the length of DNA migration increased with increasing of dosage of lead acetate.
      Conclusion   Lead acetate might cause DNA damage of rat neural cells.The damage was positive correlative with the lead dosage.The single cell gel electrophoresis test was a useful tool for deter mining the geno toxicity and apoposis of neural cells.

     

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