陈龙, 马骋, 蔡宝昌, 陆跃明, 吴皓. 乌头碱对大鼠心肌细胞钙通道阻滞作用的单通道分析J. 药学学报, 1995, 30(3): 168-171.
引用本文: 陈龙, 马骋, 蔡宝昌, 陆跃明, 吴皓. 乌头碱对大鼠心肌细胞钙通道阻滞作用的单通道分析J. 药学学报, 1995, 30(3): 168-171.
L Chen, C Ma, BC Ca, YM Lu , H Wu, . SINGLE CHANNEL ANALYSIS OF ACONITINE BLOCKADE OF CALCIUM CHANNELS IN RAT MYOCARDIOCYTESJ. Acta Pharmaceutica Sinica, 1995, 30(3): 168-171.
Citation: L Chen, C Ma, BC Ca, YM Lu , H Wu, . SINGLE CHANNEL ANALYSIS OF ACONITINE BLOCKADE OF CALCIUM CHANNELS IN RAT MYOCARDIOCYTESJ. Acta Pharmaceutica Sinica, 1995, 30(3): 168-171.

乌头碱对大鼠心肌细胞钙通道阻滞作用的单通道分析

SINGLE CHANNEL ANALYSIS OF ACONITINE BLOCKADE OF CALCIUM CHANNELS IN RAT MYOCARDIOCYTES

  • 摘要: 用膜片钳法,在培养的Wistar大鼠心室肌细胞上记录了L型钙通道的单通道活动。乌头碱50μg·ml-1能显著阻断L型钙通道的活动,使其开放时间缩短、关闭时间延长、开放概率下降。与对照组比较,有显著性统计学差异(P<0.01)。而对通过L型钙通道的钡离于流幅值无明显影响。

     

    Abstract: Ventricular myocardiocytes from neonatal Wistar rats were isolated and cultured.Aconitine,Ca2+ channel blocker verapamil or Ca2+ channel activator BAY K8644 were added to thebath solution separately. Using the cell-attached configuration of the patch clamp technique ,the singlechannel activities of L type Ca2+ channel were recorded before and after addition of all three drugs.The results showed the blocking effect of aconitine (50μg· ml-1)on L type Ca2+ channels. Itsmechanism may be relevant to the decrease in both open state probability and the mean open time ofCa2+ channel. The difference was statistically significant compared with control group(P<0.01).The amplitude of Ba2+ currents ,which flow through open L type Ca2+ channel was unchanged.

     

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