刘艳, 王硕, 吴冠宇, 赵淑华. 纳米氧化石墨烯对小鼠心肌氧化损伤作用[J]. 环境卫生学杂志, 2015, 5(3): 206-210. DOI: 10.13421/j.cnki.hjwsxzz.2015.03.005
    引用本文: 刘艳, 王硕, 吴冠宇, 赵淑华. 纳米氧化石墨烯对小鼠心肌氧化损伤作用[J]. 环境卫生学杂志, 2015, 5(3): 206-210. DOI: 10.13421/j.cnki.hjwsxzz.2015.03.005
    LIU Yan, WANG Shuo, WU Guanyu, ZHAO Shuhua. Effect of Nano Graphene Oxide on Oxidative Injury of Mice Myocardium[J]. Journal of Environmental Hygiene, 2015, 5(3): 206-210. DOI: 10.13421/j.cnki.hjwsxzz.2015.03.005
    Citation: LIU Yan, WANG Shuo, WU Guanyu, ZHAO Shuhua. Effect of Nano Graphene Oxide on Oxidative Injury of Mice Myocardium[J]. Journal of Environmental Hygiene, 2015, 5(3): 206-210. DOI: 10.13421/j.cnki.hjwsxzz.2015.03.005

    纳米氧化石墨烯对小鼠心肌氧化损伤作用

    Effect of Nano Graphene Oxide on Oxidative Injury of Mice Myocardium

    • 摘要:
      目的 观察纳米氧化石墨烯对小鼠心肌的氧化损伤作用。
      方法 选择80只健康ICR小鼠, 雌雄各半, 随机分成4组, 将纳米氧化石墨烯在无菌条件下溶于灭菌高纯水中, 分别以剂量为0、0.35、0.7和1.40 mg/kg的纳米氧化石墨烯进行尾静脉注射1次。于注射后3 d和15 d分别处死40只小鼠, 取心肌, 测定心肌组织匀浆中丙二醛(MDA)的水平、总抗氧化能力(T-AOC)、谷胱甘肽过氧化物酶(GSH-Px)活力、超氧化物歧化酶(SOD)活力。
      结果 注射后3 d, 雌、雄各剂量组MDA含量高于对照(P < 0.05);雄性高剂量组T-AOC显著低于其他组(P < 0.05);雌、雄小鼠各剂量组SOD活性均显著高于对照组(P < 0.05), 雌性小鼠具有剂量-效应关系; 雌、雄小鼠GSH-Px各剂量组均低于对照组(P < 0.05)。染毒后15 d, 雌性和雄性小鼠中、高剂量组MDA仍明显高于对照组(P < 0.05);雄性中、高剂量组T-AOC显著低于对照组和低剂量组(P < 0.05), 雌性各剂量明显低于对照组(P < 0.05);雌、雄小鼠SOD活性随剂量而增高(P < 0.05), 雌性各剂量组均明显高于对照组(P < 0.05);雌、雄小鼠各剂量组GSH-Px活性显著低于对照组(P < 0.05)。
      结论 未经修饰的纳米氧化石墨烯经尾静脉注射后可能对心肌产生脂质过氧化损伤作用。

       

      Abstract:
      Objective To observe the oxidative injury of myocardium in mice induced by nano graphene oxide.
      Methods Eighty healthy male and female ICR mice were randomly divided into four groups. Nano grapheme oxide was dissolved in sterile pure water under aseptic conditions, and it was injected intravenously only for once; the dose for each group was 0, 0.35, 0.70 and 1.40 mg/kg, respectively. Forty mice were sacrificed 3 days and 15 days after the injection, and the heart muscle of mice was collected to measure malondialdehyde (MDA) levels, total antioxidant capacity (T-AOC), the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px).
      Results At 3 days after injection, the levels of MDA in all nano grapheme oxide groups were higher than that in the control group both in male and female mice (P < 0.05); T-AOCs in high dose groups were obviously lower than that in other groups(P < 0.05); SOD activities in all nano grapheme oxide groups were higher than that in the control group both in male and female mice (P < 0.05) and a dose-effect relationship was shown in female mice; the activities of GSH-Px in all nano grapheme oxide groups were higher than that in the control group (P < 0.05). At 15 days after injection, MDA contents in the middle and high dose groups were higher than that in the control group both in male and female mice (P < 0.05); T-AOCs in the middle and high dose male groups were obviously lower than that in the control and low dose male groups (P < 0.05), T-AOCs in all nano grapheme oxide female groups were lower than that in the control group (P < 0.05); the activities of SOD in all nano grapheme oxide groups were higher than that in the control group (P < 0.05) and were rising with the dose of nano grapheme oxide in male and female mice (P < 0.05); the activities of GSH-Px in all nano grapheme oxide groups were higher than that in the control group both in male and female mice (P < 0.05).
      Conclusion Intravenous injection of unmodified nano grapheme oxide might induce lipid peroxidation injury of myocardium in mice.

       

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