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首页> 外文期刊>Japanese Journal of Pharmacology >Frequency- and Time-Dependent Effects of Fendiline on Action Potentials of Guinea Pig Papillary Muscle
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Frequency- and Time-Dependent Effects of Fendiline on Action Potentials of Guinea Pig Papillary Muscle

机译:芬迪林对豚鼠乳头肌动作电位的频率和时间依赖性作用

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References(16) Cited-By(1) The action of fendiline on cardiac electrical activity was investigated in guinea pig papillary muscle by monitoring frequency− and time−dependent changes in membrane potential, action potential(AP)configuration and conduction velocity.Isolated guinea pig papillary muscles driven at 0.1 to 3 Hz showed a concentration−dependent reduction of + Vmax, overshoot, and AP duration at −20mV(APD20)in the presence of fendiline(1−320μM), reflecting inhibition of Na+ and L−type Ca2+ channels, respectively.No significant change in resting potential and AP duration at 90% repolarization(APD90)were observed.Inhibition of + Vmax and APD20 was more prominent at higher frequency of stimulation(2 Hz)than at lower ones(0.2 Hz), demonstrating frequency−dependent block of Na+ and Ca2+ channels including an open channel block.A good relationship between changes in + Vmax and APD20 suggested some commonality in the mechanism of inhibition of Na+ and Ca2+ channels by fendiline.Time−dependence of effects of fendiline, observed in presence of bolus dose(200μM), showed an earlier onset of inhibition of + Vmax and APD20, particularly at higher frequencies.Missed beats and conduction block also appeared earlier in preparations driven at higher frequency.These findings suggest a frequency−dependent(and open channel)block of Na+ and Ca2+ channels by fendiline, leading to inhibition of fast and slow conduction in addition to its reported inactivated Ca2+ channel block.
机译:参考文献(16)(1)通过监测膜电位,动作电位(AP)构型和传导速度随频率和时间变化的变化,研究了豚鼠乳头肌中芬迪林对心脏电活动的作用。在存在芬迪林(1-320μM)的情况下,以0.1至3 Hz的频率驱动的猪乳头肌在+20 mV(APD20)下表现出+ Vmax,过冲和AP持续时间的浓度依赖性降低,反映了对Na +和L型Ca2 +的抑制在90%复极化(APD90)下未观察到静息电位和AP持续时间的显着变化。在较高的刺激频率(2 Hz)下,+ Vmax和APD20的抑制作用比在较低的刺激频率(0.2 Hz)上更为明显。展示了频率依赖性的Na +和Ca2 +通道的阻滞,包括一个开放通道阻滞+ Vmax和APD20变化之间的良好关系表明芬迪林抑制Na +和Ca2 +通道的机理存在某些共性。在大剂量(200μM)的剂量下观察到的芬迪林效应的出现表明,+ Vmax和APD20的抑制作用较早发生,特别是在较高频率下。在较高频率的制剂中,缺失的搏动和传导阻滞也较早出现。芬迪林提出Na +和Ca2 +通道的频率依赖性(和开放通道)阻滞作用,除了据报道的灭活的Ca2 +通道阻滞外,还导致抑制快慢传导。

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