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作 者:程何祥[1] 张荣庆[1] 贾国良[1] 王海昌[1] 郭文怡[1] 张殿新[1] 刘兵[1] 张清[1]
出 处:《解放军医学杂志》2004年第7期597-599,共3页Medical Journal of Chinese People's Liberation Army
摘 要:目的 研究过氧化氢 (H2 O2 )对心肌细胞[Ca2 + ]i的影响 ,以及卡维地洛对H2 O2 诱导钙超载的拮抗作用。方法 采用SD大鼠乳鼠进行心肌细胞培养。实验分为 4组 :正常对照组 ;H2 O2 组 :加入终浓度为 10 0 μmol/L的H2 O2 ;卡维地洛组 :加入终浓度为 1μmol/L的卡维地洛 ;H2 O2 +卡维地洛组 :同时加入卡维地洛 1μmol/L与H2 O2 10 0 μmol/L。以Fluo 3/AM荧光指示剂负载 ,应用激光共聚焦显微镜技术 ,分别于加入H2 O2 后即刻和 15min时检测 [Ca2 + ]i的变化。结果 对照组和卡维地洛组心肌细胞内荧光强度和荧光光密度值较低。一加入H2 O2 ,细胞内荧光光密度值便开始增加 ,15min后细胞内荧光强度和荧光光密度值较对照组显著增高 (P <0 0 5 )。而H2 O2 +卡维地洛组细胞内荧光光密度值显著低于H2 O2 组 (P <0 0 5 )。结论 H2 O2 可引起心肌细胞内钙超载 ,卡维地洛能显著减轻H2 O2 诱导的心肌细胞内Ca2 +Objective To examine effects of hydrogen peroxide on intracellular free calcium concentration(i) in cardiac myocytes and its antagonism by carvedilol. Methods A cell culture of neonatal rat cardiac myocytes was used for experimentation. They were divided into four groups, i.e. control group, hydrogen peroxide (H 2O 2) group, carvedilol group,and H 2O 2 + carvedilol group. Confocal microscope was used with Fluo-3/AM as calcium indicator to detect changes in i immediately and 15 minutes after H 2O 2 intervention, respectively. Results The intracellular fluoresence intensity of a single cardiae myocyts in the control group and carvedilol group was low. The intracellular fluoresence intensity of a single cardiac myocyte in H 2O 2 group was significantly higher than in the control group 15 minutes after intervention (P<0.05). When carvedilol was added simultaneously with H 2O 2, the values were much lower compared with H 2O 2 group (P<0.05). Conclusion Hydrogen peroxide induces intracellular calcium overload in cardiac myocytes, and carvedilol can decrease i overload in the cells induced by hydrogen peroxide.
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