基础医学与临床 ›› 2012, Vol. 32 ›› Issue (4): 386-389.

• 研究论文 • 上一篇    下一篇

金属氧化物材料对小鼠急性肺损伤作用的研究

孙婷婷,蒋澄宇   

  1. 北京协和医学院基础医学研究所
  • 收稿日期:2011-12-19 修回日期:2012-02-22 出版日期:2012-04-05 发布日期:2012-03-21
  • 通讯作者: 蒋澄宇 E-mail:jiang@pumc.edu.cn
  • 基金资助:
    国家自然科学基金

A study of the acute pulmonary injury effects of metal oxide materials in mice

  • Received:2011-12-19 Revised:2012-02-22 Online:2012-04-05 Published:2012-03-21

摘要: 摘要:目的 以C57 BL/6小鼠为模型对氧化铜、氧化铁、氧化钛、氧化硅等金属氧化物纳米材料的呼吸系统毒性进行比较和评估。方法 给C57 BL/6小鼠气管注射金属氧化物纳米材料,对给药后小鼠的死亡率、肺湿干比以及小鼠肺泡灌洗液中细胞因子的水平进行检测。结果 注射较高剂量氧化铜纳米材料的小鼠在24 h 内全部死亡,而相同剂量下注射其他金属氧化物未导致小鼠死亡;注射氧化铜纳米的小鼠肺湿干比显著高于对照组,且小鼠肺泡灌洗液中白细胞介素6的水平显著上升,而其他金属氧化物并未导致小鼠肺湿干比或白细胞介素6的水平的显著升高。结论 氧化铜纳米材料对C57 BL/6小鼠具有很强的致死性,并且引起小鼠肺水肿,导致小鼠急性肺损伤。而其他几种金属氧化物纳米材料的毒性较低,对小鼠的急性肺损伤作用较小。炎症因子IL-6水平在注射氧化铜纳米后显著增加,可能在氧化铜诱导的急性肺损伤中起到重要作用。

关键词: 氧化铜, 金属氧化物, 纳米材料, 肺损伤

Abstract: Abstract: Objective To compare and evaluate the pulmonary toxic potential of metal oxide nanoparticles (NPs), including copper oxide, ferric oxide, titanium oxide and silica in C57/BL6 mice. Methods C57/BL6 mice were exposed to metal oxide NPs via intra-tracheal instillation. Mice survival rate, lung wet-dry ratio and the expression level of cytokines in mice BAL fluid were evaluated. Results All mice died within 24 h after administration of high dose copper oxide NPs, while no mice was found dead when the same dose of the other metal oxide NPs were administered. Mice exposed to copper oxide also had significantly higher lung wet-dry ratio and higher interleukin-6 expression level in BAL fluid compared to control group. The administration of the other metal oxides did not result in significant increase of lung wet-dry ratio or elevation of IL-6 in BAL fluid compared to control group. Conclusion Copper oxide NPs demonstrated high lethality in C57/BL6, and can cause pulmonary edema, resulting in acute lung injury. In comparison, the other metal oxide NPs have much lower toxic potential and have little pulmonary injury effect in mice at the doses we used. High expression of IL-6 may play an important role in copper oxide NP-induced acute lung injury.

Key words: Copper oxide, metal oxides, nanomaterials, acute lung injury

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