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汪求真, 马爱国, 孙永叶, 周晓彬, 韩秀霞. 大剂量维生素E、C联用对细胞功能的影响[J]. 中国公共卫生, 2006, 22(9): 1053-1055. DOI: 10.11847/zgggws2006-22-09-19
引用本文: 汪求真, 马爱国, 孙永叶, 周晓彬, 韩秀霞. 大剂量维生素E、C联用对细胞功能的影响[J]. 中国公共卫生, 2006, 22(9): 1053-1055. DOI: 10.11847/zgggws2006-22-09-19
WANG Qiuzhen, MA Aiguo, SUN Yongye, . Effects of high dose VE and VC on cell activities in rats[J]. Chinese Journal of Public Health, 2006, 22(9): 1053-1055. DOI: 10.11847/zgggws2006-22-09-19
Citation: WANG Qiuzhen, MA Aiguo, SUN Yongye, . Effects of high dose VE and VC on cell activities in rats[J]. Chinese Journal of Public Health, 2006, 22(9): 1053-1055. DOI: 10.11847/zgggws2006-22-09-19

大剂量维生素E、C联用对细胞功能的影响

Effects of high dose VE and VC on cell activities in rats

  • 摘要:
      目的   研究大剂量维生素E(VE)、维生素C(VC)联用对大鼠外周血淋巴细胞的增殖、抗DNA氧化损伤以及红细胞膜流动性的影响。
      方法   将Wistar大鼠随机分为6组, 即对照组、VC组〔每天1 000 mg/(kgºbw)〕、2个VE组〔每天33, 500 mg/(kgºbw)〕及2个VE、VC联合补充组, 实验期为8周。分别采用DPH荧光标记、四甲基偶氮唑盐(MTT)比色法、单细胞凝胶电脉法(SCGE)分析红细胞膜流动性、淋巴细胞转化率及DNA氧化损伤。
      结果   33mg/(kgºbw)VE可降低血浆丙二醛(MDA)水平, 提高红细胞膜谷胱甘肽过氧化物酶(GSH-Px)活力(P < 0.05);该组红细胞膜P、η值低于其它组, 即膜流动性显著改善; 淋巴细胞转化率较对照提高了146.54%;DNA氧化损伤为150.42 AU, 显著低于其它组(P均 < 0.05)。联合补充(VE1+VC)组的细胞转化、抗DNA损伤等细胞功能指标均较单独补充(VE1)组下降(P < 0.05)。
      结论   较大剂量VE能提高淋巴细胞增殖活性及抗DNA氧化损伤能力、改善红细胞膜流动性, 但大剂量VC可能对其影响产生拮抗作用; 过大剂量VE、VC补充时均未观察到有利作用, 甚至显示细胞活性下降。

     

    Abstract:
      Objective   To study the effects of high dose VE and VC on peripheral blood lymphocyte proliferation and anti-DNA oxidative damage activities and erythrocyte membrane fluidity.
      Methods   Wistar rats were randomly divided into six groups including control, VC, VE1, VE2, VE1+VC and VE2+VC groups.The trial lasted 8 weeks.Fluorescence polarization method, methyl thiazolyl tetrazolium(MTT)and comet assay were used to detect erythrocyte membrane fluidity, lymphocyte transformation rate and DNA oxidative damage respectively.
      Results   In VE1〔33 mg/(kgºd)〕group, plasma MDA was lowered while erythrocyte membrane glutathione peruxidase(GSHPx)activity increased significantly.P(fluorescence polarization)and η(microviscosity), which were inversely related with membrane fluidity, were significantly lowered.Compared with the control, lymphocyte transformation rate in VE1 group was significantly increased by 146.54% and DNA oxidative damage induced by 10μmol/1 H2O2 was significantly lowered.There was significant antagonism effect between 1 000 mg/(kgºd) VC and 33 mg/(kgºd)VE and lowered cell function was seen in the combined group.
      Conclusion   Relatively high dose VE could effectively enhance lymphocyte proliferation, DNA stability and erythrocyte membrane fluidity.Buthigh dose VC could cause antagonism effect.Too excessive VE and VC showed no favourable effects and whatever more the activities of peripheral blood cell might be decreased.

     

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