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正常浦肯野纤维与梗死存活浦肯野纤维钠电流的比较——一项药理学研究。

Comparison of the sodium currents in normal Purkinje fibres and Purkinje fibres surviving infarction--a pharmacological study.

作者信息

Bril A, Kinnaird A A, Man R Y

机构信息

Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.

出版信息

Br J Pharmacol. 1989 Aug;97(4):999-1006. doi: 10.1111/j.1476-5381.1989.tb12554.x.

Abstract
  1. Purkinje fibres surviving infarction showed a lower maximum upstroke velocity (Vmax) and a longer action potential duration when compared to normal Purkinje fibers. A reduction in the fast sodium current and an increase in the sodium 'window' current may be responsible for the observed alterations in Vmax and action potential duration respectively. 2. Since voltage clamp studies were not feasible, a pharmacological approach was used. The responses to tetrodotoxin (TTX) and lignocaine in normal Purkinje fibres and Purkinje fibres surviving infarction were used to examine the sodium currents in these fibres. 3. Vmax, an indirect measure of the fast sodium current, was more sensitive to lignocaine in Purkinje fibres surviving infarction than in normal Purkinje fibres. The reduction in Vmax by lignocaine was more prominent at the shorter stimulation cycle length. Significant reduction of Vmax was observed with the higher concentration of TTX and no differential effect on Vmax between normal Purkinje fibres and Purkinje fibres surviving infarction was detected. 4. Reduction of action potential duration in the presence of TTX or lignocaine was used as a measure of the sodium 'window' current. A greater reduction of action potential duration by TTX and lignocaine was observed in normal Purkinje fibres than in Purkinje fibres surviving infarction. 5. The results suggested that the fast sodium current in Purkinje fibres surviving infarction is more sensitive to pharmacological agents with local anaesthetic properties and the prolonged action potential duration in these Purkinje fibres cannot be due to an increase in the sodium 'window' current. The results are compatible with an enhanced effect of antiarrhythmic drugs on Vmax and conduction in the ischaemic heart.
摘要
  1. 与正常浦肯野纤维相比,梗死灶存活的浦肯野纤维表现出较低的最大上升速度(Vmax)和较长的动作电位时程。快速钠电流的减少和钠“窗”电流的增加可能分别是观察到的Vmax和动作电位时程改变的原因。2. 由于电压钳研究不可行,因此采用了药理学方法。通过观察正常浦肯野纤维和梗死灶存活的浦肯野纤维对河豚毒素(TTX)和利多卡因的反应来检测这些纤维中的钠电流。3. Vmax是快速钠电流的间接指标,梗死灶存活的浦肯野纤维对利多卡因的敏感性高于正常浦肯野纤维。在较短的刺激周期长度下,利多卡因对Vmax的降低更为显著。高浓度TTX可使Vmax显著降低,且未检测到正常浦肯野纤维与梗死灶存活的浦肯野纤维之间Vmax的差异效应。4. 在存在TTX或利多卡因的情况下动作电位时程的缩短用作钠“窗”电流的指标。与梗死灶存活的浦肯野纤维相比,正常浦肯野纤维中TTX和利多卡因使动作电位时程的缩短更为明显。5. 结果表明,梗死灶存活的浦肯野纤维中的快速钠电流对具有局部麻醉特性的药物更为敏感,这些浦肯野纤维中动作电位时程的延长并非由于钠“窗”电流的增加。这些结果与抗心律失常药物对缺血心脏中Vmax和传导的增强作用相符。

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