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作 者:包金风[1] 张晓文[2] 卢新政[2] 饶曼人[2]
机构地区:[1]徐州医学院药理教研室,江苏徐州221004 [2]南京医科大学药理教研室,江苏南京210029
出 处:《甘肃医药》2010年第2期121-124,共4页Gansu Medical Journal
摘 要:目的:研究参三七皂苷Rb1、Rg1药理性预适应对乳鼠肥厚心肌细胞缺氧/复氧损伤(A/R)细胞凋亡的影响。方法:采用血管紧张素Ⅱ诱导的肥厚心肌细胞A/R模型,心肌细胞随机分组:空白对照组,A/R模型对照组(组),参三七皂苷Rb1、Rg10.01—10μmol/L药物预适应组(预适应48h后进行A/R处理);用流式细胞术观察心肌细胞凋亡率,电镜观察细胞超微结构。结果:与A/R对照组相比参三七皂苷Rb1、Rg10.0110μmol/L预适应48h后,细胞凋亡率呈浓度依赖性下降,Rb1、Rg1最大凋亡抑制率分别为86.68%和85.26%(P〈0.01)。电镜超微结构观察显示参三七皂苷Rb1、Rg1组细胞凋亡明显减轻,细胞结构完整,细胞基本结构无损害。结论:参三七皂苷Rb1、Rg1药理性预适应具有明显抑制细胞凋亡、改善心肌细胞缺氧/复氧损伤作用。Objective: To investigate the effect of Panax notoginsenoside Rb1 and Rg1 pharmacologic preconditioning on apeptosis in hypoxia/reoxygenation(A/R) injury in angiotensin Ⅱ induced hypertrophic myocardial cells of neonatal rat. Methods: Myocardial cells were divided into control group, A/R model group, Panax notoginsenoside RbI and Rg1 drug preconditioning groups (with Rb1 and Rgl0. 01 - 10μmol/L before A/R 48h ). Apoptotic rate of myocardial cells were observed with flow cytometry, ultrastructure of myocardial cells were observed with electron microscope. Results: Apoptotic rate of myocardial cells of 0.01 - 10μmol/L Panax notoginsenoside Rb1 and Rg1 concentration - dependent decreased after 48h of preconditioning in which the maximum apoptoSe rate was 86.68 % and 85.26 % respectively ( P 〈 0. 01), cell basic structure of panax notoginsenoside Rbt and RgI groups integrated in ultrastructure with electron microscope. Conclusion: Panax notoginsenoside Rb1 and Rg1 pharmacologic preconditioning can obviously inhibit apeptosis in angiotensin Ⅱ induced hypertrophied neonatal rat myocytes, which improved protective effect for myocardial hypoxia/reoxygenation injury.
关 键 词:参三七皂苷Rb1、Rg1 缺氧/复氧损伤 细胞凋亡 预适应
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