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作 者:崔琳[1] 高维奇[1] 刘平[1] 张红[1] 于莉[1] 关立南[1]
机构地区:[1]哈尔滨医科大学第一附属医院眼科医院眼科三病房,黑龙江哈尔滨150001
出 处:《中国伤残医学》2007年第5期17-19,共3页Chinese Journal of Trauma and Disability Medicine
摘 要:目的:研究丹参对体外培养的兔晶状体氧化损伤的保护作用。方法:应用单细胞凝胶电泳法分别测定了0.1mg/ml、0.5mg/ml、1mg/ml浓度丹参液对体外培养72h后晶状体上皮细胞氧化损伤的保护作用,并测定晶状体中SOD、MDA含量。结果:各浓度丹参培养组相对于H2O2培养组晶状体的氧化损伤均有不同程度减轻,1mg/ml丹参剂量组的保护作用更为明显,其尾长、彗星细胞百分率及SOD、MDA含量与对照组相比无显著差异(P>0.05),对照组及各处理组与H2O2培养组相比各指标均有显著差异(P<0.001)。结论:丹参中的有效成分对体外培养的晶状体氧化损伤有明显的保护作用,且呈现剂量依赖的量效关系。Objective:To investigate the protection of Tan-shen on H2O2-induced lens damage of rabbit. Method: The protection of 0.1mg/ml, 0.5mg/ml, lmg/ml Tan-shen on H2Oa-induced lens epithelial cells damage was detected with single cell gel electrophoresis assay at 72 hours after culture in vitor ,and detected the contents of SOD, MDA in lens. Results:The various concentration groups of Tan-shen were significantly increased campared H2O2-induced group, 0.8mg/ml group have an advantage on other groups.There was not significant differece with control groups in tail DNA%, tail length and the contents of SOD, MDA(P〉0.05), there was great significant differece at treatment groups and damage groups in various indexs(P〈0.001). Conclusion: Tan-shen could protect lens epithelial cells against oxidative stress. Its effect might be dose-dependent.
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