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覃容贵, 吴建伟, 国果, 付萍. 蝇蛆壳聚糖对H2O2致内皮细胞损伤保护作用[J]. 中国公共卫生, 2011, 27(10): 1275-1276. DOI: 10.11847/zgggws-2011-27-10-24
引用本文: 覃容贵, 吴建伟, 国果, 付萍. 蝇蛆壳聚糖对H2O2致内皮细胞损伤保护作用[J]. 中国公共卫生, 2011, 27(10): 1275-1276. DOI: 10.11847/zgggws-2011-27-10-24
QIN Rong-gui, WU Jian-wei, GUO Guo, . Protective effect of housefly maggot chitosan on brain microvascular endotheliocyte[J]. Chinese Journal of Public Health, 2011, 27(10): 1275-1276. DOI: 10.11847/zgggws-2011-27-10-24
Citation: QIN Rong-gui, WU Jian-wei, GUO Guo, . Protective effect of housefly maggot chitosan on brain microvascular endotheliocyte[J]. Chinese Journal of Public Health, 2011, 27(10): 1275-1276. DOI: 10.11847/zgggws-2011-27-10-24

蝇蛆壳聚糖对H2O2致内皮细胞损伤保护作用

Protective effect of housefly maggot chitosan on brain microvascular endotheliocyte

  • 摘要: 目的 研究蝇蛆壳聚糖(HMC)对过氧化氢(H2O2)诱导的内皮细胞氧化应激损伤的保护作用。方法 利用H2O2诱导的内皮细胞损伤模型,采用不同剂量HMC预培养,通过四甲基偶氮噻唑蓝(MTT)比色法检测细胞存活率,生化法和放免法检测细胞培养液超氧化物歧化酶(SOD)和丙二醛(MDA)、一氧化氮(NO)和内皮素(ET)水平。结果 中、高剂量HMC组细胞存活率A值分别为(0.714 0±0.059 5)、(0.811 9±0.059 7),均高于H2O2 损伤组(0.597 2±0.042 2)(P<0.01);低、中、高剂量HMC组细胞SOD活性分别为(14.76±1.59)、(16.99±1.69)、(19.22±2.31)NU/mL,明显高于H2O2损伤组(P<0.05,P<0.01);低、中、高剂量HMC组细胞MDA含量分别为(10.11±1.91)、(8.23±1.64)、(6.74±1.26)nmol/L,明显低于H2O2损伤组(P<0.01);各剂量HMC组细胞NO水平明显高于H2O2损伤组,而ET含量则明显低于H2O2损伤组(P<0.01)。结论 HMC具有保护血管内皮细胞的作用,机制可能与减少细胞NO释放、增加ET水平、维护内皮细胞结构和功能完整及增强其抗氧化能力有关。

     

    Abstract: Objective To study the protective effect of housefly maggot chitosan(HMC)on the damage of brain microvascular endotheliocyte induced by H2O2 in vitro.Methods Normal cells,damaged cells induced by H2O2 were cultured in modified minimal essential medium(DMEM),together with different doses of HMC.The survival rates of the cells were tested with 3-(4,5 dimethythiazol-2-yl)-2,5 diphenyl-tetrazolium bromide(MTT)assay.Vasoactive substance contents such as nitric oxide(NO)and endothelin(ET)in cell culture fluid were tested with biochemistry and radioimmunity method.In addition,superoxide dismutase(SOD)and malonodialdehyde(MDA)contents in culture fluid of H2O2 damaged cells were detected with biochemistry method.Results In MTT experiment,A values for cell survival rate of moderate and high dose HMC+hydrogen peroxide groups were 0.714 0±0.059 5 and 0.811 9±0.059 7,which were higher than that of hydrogen peroxide treated groups(P<0.01).In all HMC+hydrogen peroxide groups,SOD levels were 14.76±1.59, 16.99±1.69,and 19.22±2.31NU/mL,respectively,which were higher than those of hydrogen peroxide treated groups (P<0.05,P<0.01).In all HMC+hydrogen peroxide groups,MDA levels were 10.11±1.91,8.23±1.64,and 6.74±1.26 nmol/L,respectively,which were lower than that of hydrogen peroxide treated groups(P<0.01).NO levels were higher (P<0.05,P<0.01)and ET contents were lower(P<0.01)than those of H2O2 treated group(P<0.01).Conclusion HMC could protect vascular endothelial cell and could elevate cell survival rate,promote the releasing of NO from damaged cell induced by H2O2,restrain the releasing of ET,preserve the structural and functional integrity of the cell.HMC could activate SOD,enhance its anti-oxidation effect.

     

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