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作 者:战术[1] 钟国赣[1] 安刚[1] 孙成文[1] 曾庆华[1] 孙晓霞[1] 邵春杰[1] 徐景达[1]
机构地区:[1]白求恩医科大学生理教研室 生理中心实验室 有机化学教研究室
出 处:《中国药学杂志》1996年第7期401-403,共3页Chinese Pharmaceutical Journal
摘 要:目的:观察刺五加皂苷单体Sc3(AcanthopanaxSenticosideC3)对培养的Wistar大鼠乳鼠心肌细胞自发性搏动及动作电位电参数的影响。方法:将50~800μg/mlSc3,分别加入到培养4~6d后的Wistar大鼠乳鼠心肌细胞的培养液中,依次记录加药前、后自发性搏动及动作电位电参数的变化。结果:Sc3可剂量依赖性地抑制被培养的Wistar大鼠乳鼠心肌细胞的自发性搏动及动作电位的电参数,其作用与0.4μg/ml尼莫地平相似,而该作用被80μg/mlCa2+所反转。OBJECTIVE:To observe the influence of Sc 3(Acanthopanax senticoside C 3)on the spontaneous conrtractility and the electricalparameters of action potential of the cultured neonatal Wistar rat myocardicytes :50~800 μg/ml Sc 3 was added into the culture fluid of the neonatal Wistar rat myocardiocytes 4~6 days after culture,and then the changes of the spontaneous contractility and the electrical parameters of action potential recorded after and before administration.RESULTS:Sc 3 inhibited the spontaneous contractility and the electrical parameters of action potential of the cultured neonatal Wistar rat myocardiocytes dose dependently,which was similar to that of 0.4 μg/ml nimodipine,however,could be reversed by 80 μg/ml Ca 2+ .CONCLUSION:Sc 3 could block calcium channel.
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