1. 吉林医药学院,吉林吉林,132013
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朱文赫, 张巍, 秦迎新, 等. 胡桃楸青皮萃取物对内源性H2O2诱导的血管内皮细胞损伤的保护作用研究[J]. 上海中医药杂志, 2015,49(2):78-81.
ZHU Wen-he, ZHANG Wei, QIN Ying-xin, et al. Protective effects of the extract of Juglans mandshurica maxim on endothelial cell damage induced by endogenous H2O2[J]. Shanghai Journal of Traditional Chinese Medicine, 2015,49(2):78-81.
朱文赫, 张巍, 秦迎新, 等. 胡桃楸青皮萃取物对内源性H2O2诱导的血管内皮细胞损伤的保护作用研究[J]. 上海中医药杂志, 2015,49(2):78-81. DOI:
ZHU Wen-he, ZHANG Wei, QIN Ying-xin, et al. Protective effects of the extract of Juglans mandshurica maxim on endothelial cell damage induced by endogenous H2O2[J]. Shanghai Journal of Traditional Chinese Medicine, 2015,49(2):78-81. DOI:
目的:探讨胡桃楸青皮萃取物对内源性H,2,O,2,诱导血管内皮细胞凋亡的影响 方法:建立10 mU葡萄糖氧化酶(GOX)催化生成内源性H,2,O,2, 损伤内皮细胞模型。①将细胞分成空白对照组、10 mU GOX组及实验组(10 mU GOX与25 mg/ L、50 mg/ L、100 mg/ L浓度的萃取物共培养)共5组,分别进行相应干预,观察不同剂量胡桃楸青皮萃取物对血管内皮细胞形态学及细胞增殖影响。②将细胞分成空白对照组、10 mU GOX组、10 mU GOX+50 mg/ L萃取物混合培养组,分别进行相应干预。采用Hoechst 33258荧光染色法观察细胞凋亡的形态学改变;Annexin / PI 双标记染色后进行流式细胞双色分析,检测内皮细胞凋亡率 结果:①与空白对照组比较,10 mU GOX组,10 mU GOX组与25 mg/L、50 mg/L、100 mg/L混合培养组细胞存活率差异有统计学意义(P<0.05,P<0.01);10 mU GOX组与25 mg/L、50 mg/L、100 mg/L混合培养组细胞存活率明显高于10 mU GOX组(P<0.05,P<0.01)。② Hoechst 33258荧光染色及早期凋亡率分析显示,与空白对照组比较,10 mU GOX组细胞凋亡率显著升高,差异有统计学意义(P,<,0.01);与10 mU GOX组比较,10 mU GOX+50 mg/ L 萃取物组细胞凋亡率显著升高,差异有统计学意义(P,<,0.01) 结论:胡桃楸青皮萃取物对内源性H,2,O,2,损伤的血管内皮细胞有保护作用,进一步研究表明胡桃楸青皮萃取物对内源性H,2,O,2,诱导的内皮细胞凋亡有抑制作用。
Objective:To investigate the effect of extract of Juglans mandshurica maxim on apoptosis of endothelial cells induced by endogenous H,2,O,2, in vitro Methods:Endothelial cells induced by endogenous H,2,O,2, cells were cultured by incubating with 10 mU GOX. ① Cells were divided into the blank control group, 10 mU GOX group, and experimental groups by different concentrations (10 mU GOX and 25 mg/L, 50 mg/L, 100 mg/L extract). Each group was treated with the corresponding measures. The effect of Juglans mandshurica maxim on morphology and proliferation of vascular endothelial cells were detected. ② Cells were divided into the blank control group, 10 mU GOX group and 10 mU GOX+50 mg/ L extract group, and each group was treated with the corresponding measurements. The apoptotic cells were detected by Hoechst 33258 Assay Kit, and apoptotic percent was measured by flow cytometry (FCM) after Annexin / PI double staining Results: ① Compared with the blank control group, there were significant differences in the cell survival rate in the 10 mU GOX group, 10 mU GOX+25 mg/L, 50 mg/L and 100 mg/L groups (P<0.05, P<0.01). The cell survival rates in the 10 mU GOX+25 mg/L, 50 mg/L and 100 mg/L groups were higher than that of the 10 mU GOX group (P<0.05, P<0.01). Results: of Hoechst33258 fluorescence staining showed that:compared with the blank control group, apoptosis rate in the 10 mU GOX group was increased significantly (P,<,0.01); compared with the 10 mU GOX group, apoptosis rate in the 10 mU GOX+50 mg/L group was increased markedly (P,<,0.01) Conclusion:The extract of Juglans mandshurica maxim can protect the cells significantly, which indicate that it has inhibiting effect on cell apoptosis induced by endogenous H,2,O,2,.
胡桃楸细胞凋亡过氧化氢
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