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韩磊, 马爱国, 梁惠. 不同剂量维生素A摄入对大鼠DNA损伤的影响[J]. 中国公共卫生, 2004, 20(8): 943-945.
引用本文: 韩磊, 马爱国, 梁惠. 不同剂量维生素A摄入对大鼠DNA损伤的影响[J]. 中国公共卫生, 2004, 20(8): 943-945.
HAN Lei, MA Ai-guo, LIANG Hui. Influence of vitamin A intake of different dosage on DNA damage in rats[J]. Chinese Journal of Public Health, 2004, 20(8): 943-945.
Citation: HAN Lei, MA Ai-guo, LIANG Hui. Influence of vitamin A intake of different dosage on DNA damage in rats[J]. Chinese Journal of Public Health, 2004, 20(8): 943-945.

不同剂量维生素A摄入对大鼠DNA损伤的影响

Influence of vitamin A intake of different dosage on DNA damage in rats

  • 摘要:
      目的   探讨补充不同剂量维生素A(VA)对DNA氧化及烷化损伤的影响。
      方法   将Wistar大鼠随机分为4组, 分别为VA缺乏组, 及补充VA11.43, 42.86, 142.86μgRE(视黄醇当量)/(kg°d)3个剂量组。干预时间为8周。采用单细胞凝胶电泳法(SCGE)分析比较不同组之间淋巴细胞DNA氧化损伤; 用高效毛细管电泳法测定尿中O6-甲基鸟嘌呤(O6-Methyl-guanine, O6-MeG)的排出量。
      结果   DNA损伤分析显示VA缺乏组淋巴细胞DNA自发性损伤明显高于VA补充组(P < 0.01)。用H2O2诱导淋巴细胞氧化损伤时, 4286μgRE/(kg°d)组的淋巴细胞损伤最轻(P < 0.01)。缺乏组大鼠尿中的O6-MeG的排出量随缺乏时间的延长明显升高(P < 0.01)。42.86μgRE/(kg°d)组O6-MeG的排出量无明显改变。142.86μgRE/(kg°d)组至第8周时, O6-MeG的排出量分别为VA缺乏组、11.43和42.86μgRE/(kg°d)组的1.38倍(P < 0.05)、3.57倍(P < 0.01)和11.75倍(P < 0.01)。
      结论   较长时间VA缺乏可导致机体DNA自发性损伤、H2O2诱导的氧化损伤及DNA烷化损伤均明显增加; 高剂量142.86μgRE/(kg°d)VA补充对DNA损伤不但无防护作用, 反而增加DNA损伤; 适量摄入42.86μgRE/(kg°d)的VA能有效地增强DNA抗氧化和烷化损伤的能力。

     

    Abstract:
      Objective   To investigate the effect of VA supplement with a different dosage on oxidative DNA daaTage and Oe-MeG adduct in rats.
      Methods   Wistar rats selected for VA supplement trial, were randomly divided into four groups.The first group was no VA supplement as a control, and UTe second, third, forth groups were daily supplemented with 11.43, 42.863, 142.863μgRE(Retinol Equivalent)/(kg°d)respectively.DNA oxidative damage in the four groups were detected by single-cell gel electrophoresis(SCGE)and Oe-Methyl-guanine(O6-MeG)was measured by high performance capillary zone electrophoresis.
      Results   The result of DNA damage showed that intrinsic damage of DNA was more severe in the group of vitamin A deficiency than the groups supplemented with vitamin A(P < 0.01).The lowest damage of oxidative DNA damage reduced by H2O2 was found in 42.863μg RE/(kg°d)group(P < 0.01).O6-MeG level in the group of vitamin A deficiency increased significantly chaperonage extending of the supplement deficiency(P < 0.01).O6-MeG level was not nearly change in 42.863μg RE/(kg°d)group in the period of trial.In 142.863μg RE/(kg°d)group O6-MeG level which was significantly higher than deficiency and other two groups in the end of the trial, which was 1.38 times in the first (P < 0.05), 3.57 times in the second(P < 0.01)and 11.75 times in the third groups respectively(P < 0.01).
      Conclusion   If retinol deaciency for a long time can cause or promote DNA damage.Overake retinol did not pretect DNA damage and could produce a strong poisoning effect.A moderate amount such as 42.863μg RE/(kg°d)could enhance the ability of antioxidation and mitigating DNA damage.

     

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