癌变·畸变·突变 ›› 2004, Vol. 16 ›› Issue (4): 226-228.doi: 10.3969/j.issn.1004-616x.2004.04.012

• 论著 • 上一篇    下一篇

钬元素对小鼠肝脏细胞DNA损伤的影响

汪承润,闵 莉, 吴 薇,薄 军   

  1. 淮南师范学院化学生物系,安徽 淮南 232001
  • 收稿日期:2004-01-02 修回日期:2004-05-08 出版日期:2004-07-30 发布日期:2004-07-30
  • 通讯作者: 汪承润

Effects of Holmium Element on DNA Lesion of Mice Liver Cells in Vivo

WANG Cheng-run, MIN Li, WU Wei, et al   

  1. Department of Chemistry and Biology, Huainan Normal College, Huainan 232001,China
  • Received:2004-01-02 Revised:2004-05-08 Online:2004-07-30 Published:2004-07-30
  • Contact: WANG Cheng-run

摘要: 背景与目的: 通过研究钬离子溶液对小鼠肝脏细胞DNA的损伤,探讨钬元素对诱导动物细胞凋亡的影响 。材料与方法: 处理组1: 小鼠定时灌胃氯化钬溶液50 mg/(kg•d),连续5 d; 组 2~3: 小鼠分别定时腹腔注射氯化钬溶液60 mg/(kg•d)和120 mg/(kg•d),连续2 d; 组4: 小鼠一次性腹腔注射氯化钬溶液320 mg/kg; 每次染毒相间24 h,组1~4: 小鼠均在末次染毒24 h后处死,提取肝脏DNA。 组5: 小鼠一次性腹腔注射等体积生理盐水; 组6~9: 小鼠一次性腹腔注射氯化钬溶液80 mg/kg,分别于注射后12、24、48和96 h处死小鼠提取肝脏DNA。通过琼脂糖凝胶电泳研究各组DNA带型变化。 结果:处理组7 DNA电泳中出现连续的弥散带型,其它各组均未观察到明显的拖尾现象。也未观察到“DNA ladder"。 结论: 钬离子对小鼠肝脏细胞DNA的断裂作用可能与其剂量大小、处理时间及DNA修复作用有关,而且无特异性。本实验结果表明,钬元素未诱导小鼠肝脏细胞凋亡。

关键词: 钬元素, DNA损伤, DNA ladder, DNA修复, 细胞凋亡

Abstract: BACKGROUND & AIM: To study the effect of holmium ions on DNA breakage of mice liver cells and the effect of holmium element on apoptosis of zoic cells in vivo. MATERIAL AND METHODS: Group 1: Mice were administered orally with daily dose of 50 mg/kg of holmium chloride solution for 5 days;Group 2~3: Mice were treated intraperitoneally with daily dose of 60 mg/kg and 120 mg/kg of holmium chloride solution twice respec tively. Group 4: Mice were treated intraperitoneally with a single dose of 320 mg/kg of holmium chloride solution. In group 1~3, the interval of poisoning was 24 h, and DNA was extracted from mice livers 24 h after the last poisoning in groups above. Group 5: Mice were administered intraperitoneally with the same volume of saline as below. Group 6~9: Mice were treated intraperitoneally with a single dose of 80 mg/kg of holmium chloride solution and DNA was extracted at 12, 24, 48 and 96 h respectively. Agarose gel electrophoresis was performed to observe the tapes'change. RESULTS: In group 7, a continual diffusive tailed tape was showed, but no obvious DNA-tailed tape observed in all the other groups. Meanwhile, no DNA ladder was found, too. CONCLUSIONS: It is possible that the extension of DNA breakage caused by holmium ions to mice liver cells was associated with dose, treating duration and DNA-repair, which had no specificity. The results suggest that holmium element couldn't induce apoptosis of mice liver cells in vivo in the experiments.

Key words: holmium element, DNA breakage, DNA ladder, DNA repair, apoptosis.