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薯蓣皂苷对培养乳鼠心肌细胞缺氧/复氧损伤的保护作用
引用本文:高卫真,王玮,范晓静,康毅,赵云茜,于雷,张真,吴艳娜,刘艳霞,娄建石,高文远.薯蓣皂苷对培养乳鼠心肌细胞缺氧/复氧损伤的保护作用[J].中国分子心脏病学杂志,2008,8(2):72-74.
作者姓名:高卫真  王玮  范晓静  康毅  赵云茜  于雷  张真  吴艳娜  刘艳霞  娄建石  高文远
作者单位:1. 300072,天津大学药学院;300072,天津医科大学药理学教研室
2. 天津医科大学药理学教研室,300072
3. 600041,成都,国家天然药物研究中心
4. 天津大学药学院,300072
摘    要:目的研究薯蓣皂苷对培养乳鼠心肌细胞缺氧/复氧损伤的保护作用并探讨其作用机制。方法采用体外培养乳鼠心肌细胞,建立缺氧/复氧损伤模型,以薯蓣皂苷进行干预。心肌细胞随机分为5组:空白对照组(C组);缺氧/复氧组(A/R组);薯蓣皂苷(Dioscin)低、中、高剂量干预组(Dioscin+A/R组)。分别观察各组心肌细胞搏动频率;MTr法测细胞存活率;用Rhl23荧光探针标记线粒体,检测荧光强度以反映线粒体膜电位(△ψm)变化;Fluo-3负载心肌细胞,激光扫描共聚焦显微镜观察细胞内钙离子浓度变化。结果薯蓣皂苷干预组心肌细胞搏动频率、细胞存活率、△ψm与A/R组比较明显升高;细胞内平均钙离子荧光强度显著低于A/R组。结论从细胞水平初步证实薯蓣皂苷预处理心肌细胞对A/R损伤有一定保护作用,保护机制可能涉及对线粒体膜保护和防止细胞内钙超载等。

关 键 词:薯蓣皂苷  缺氧/复氧损伤  心肌细胞  线粒体膜电位  钙超载

The Protective Effect of Dioscin on Cultured Cardiomyocytesin Anoxia/Reoxygenation Injury
GAO Wei-zhen,WANG Wei,FAN Xiao-jin,KANG Yi,ZHAO Yun-qian,YU Lei,ZHANG Zhen,WU Yan-na,LIU Yan-xia,LOU Jian-shi,GAO Wen-yuan.The Protective Effect of Dioscin on Cultured Cardiomyocytesin Anoxia/Reoxygenation Injury[J].Molecular Cardiology of China,2008,8(2):72-74.
Authors:GAO Wei-zhen  WANG Wei  FAN Xiao-jin  KANG Yi  ZHAO Yun-qian  YU Lei  ZHANG Zhen  WU Yan-na  LIU Yan-xia  LOU Jian-shi  GAO Wen-yuan
Affiliation:GA0 Wei-zhen, WANG Wei, FAN Xiao-fin, KANG Yi, ZHA0 Yun-qian, YU Lei, ZHANG Zhen, WU Yan-na, LIU Yan-xia, L0U Jian-shi, GA0 Wen-yuan. (Pharmacology department Tian-jin Medical University, Tian-jin, 300070, China)
Abstract:Objective To investigate the mechanisms of A/R and the effects of dioscin on the cul- tured myocardial cells. Methods Cultured myocardial cells of neonatal Wistar rats were randomly divided into five groups: Control group; A/R group; dioscin L, M, H group. At the end of experiment, myocardial cells beating rate, cell viability, alteration of mitochondria membrane potential (△ψm) on myocardial cells were determined by Rh123 staining method, alteration of Ca^2+ ] i on myocardial cells were determined by LSCM. Result Compared with A/R group , the beating rate, cell viability and △ψm of each dioscin group was significantly increased. Compared with AZR group, the average fluorescence intensity of Ca^2+ ] i of each dioscin group was significantly reduced. Conclusion It is suggested that dioscin may be involved in the process of protection on cultured myocardial cells in A/R injury. The protection of mitochondria membrane and prevention of calcium overload may be involved in the mechanism of dioscin-protection.
Keywords:Dioscin  Anoxia/reoxygenation (A/R) damage  Cardiomyocytes  Mitochondria mem- brane potential  Calcium overload
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