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机构地区:[1]辽宁中医药大学,沈阳110032
出 处:《山东医药》2011年第15期34-35,共2页Shandong Medical Journal
基 金:辽宁省教育厅2009年度高等学校科研项目计划项目(2009A495)
摘 要:目的探讨沙棘总黄酮对损伤人脐静脉血管内皮细胞株(CRL-1730)的保护作用。方法采用H2O2诱导CRL-1730细胞损伤模型,并将细胞随机分为四组,正常组不予任何干预;模型组加入250μmol/L H2O2;沙棘组加入沙棘总黄酮终浓度分别为50、100、200μg/m l,继续培养24 h后加入H2O2(剂量同上);丹参组加入丹参注射液终浓度2.5 mg/m l,继续培养24 h后加入H2O2(剂量同上)。细胞干预4 h后用MTT比色法检测各组细胞活性,并用流式细胞仪测定各组细胞周期。结果与正常组比较,模型组细胞增殖活性下降,S期细胞比率降低,G2/M期细胞比率增加。与模型组比较,沙棘组及丹参组细胞增殖活性升高,G0/G1期细胞比率降低,S期及G2/M期细胞比率均增加。结论沙棘总黄酮对受损血管内皮细胞有保护作用,可提高细胞增殖活性,增加S期细胞比率。Objective To investigate the protective effect of the total flavones of Hippophae Rhamnoides L(TFH) on damaged human umbilical vein endothelial cells(CRL-1730).Methods Injured model of CRL-1730 were induced by H2O2,and randomly divided into four groups,the normal group were not given any intervention;the model group was added 250 μmol/L H2O2;the TFH groups were added TFH with the final concentrations of 50,100,200 μg/ml respectively,and added H2O2(dose ditto) 24 hs after training;the Danshen group was added Danshen injection with the final concentration of 2.5 mg/ml,and added H2O2(dose ditto) 24 hs after training.Cells were intervened for 4 hs and then determined by MTT colorimetric to detect cell viability,the percentage of cell circles were detected by flow cytometry.Results Compared with the normal group,the cell viability and the percentage of S phase cells decreased,and the percentage of G2/M phase cells increased in the model group;compared with the model group,the cell viability and the percentage of S phase cells,G2/M phase cells in the TFH group and Danshen group increased,and the percentage of G0/G1 phase cells decreased.Conclusions The TFH has precise protective effect on damaged HUVECs,it can raise cell proliferation activity and increase ratio of S phase cells.
关 键 词:沙棘总黄酮 人脐静脉血管内皮细胞 细胞周期 过氧化氢
分 类 号:R329.28[医药卫生—人体解剖和组织胚胎学]
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