(Circulation. 1999;99:1637-1643.)
© 1999 American Heart Association, Inc.
Basic Science Reports |
From the First Department of Internal Medicine, Yamagata University School of Medicine, Yamagata, Japan.
Correspondence to Michiyasu Yamaki, MD, First Department of Internal Medicine, Yamagata University School of Medicine, 2-2-2 Iida-Nishi, Yamagata 990-9585, Japan. E-mail myamaki{at}med.id.yamagata-u.ac.jp
BackgroundThe electrical alternans shown on an ST segment, ST alternans, is known as one of the most important predictors of ventricular fibrillation (VF). It has also been reported that sodium channel inhibition changes action potential configuration, especially on the repolarization phase. Thus, the sodium channel blocker may produce ST alternans and trigger reentrant arrhythmia.
Methods and ResultsA sodium channel blocker (disopyramide, lidocaine, or flecainide) was infused selectively into the left anterior descending coronary artery in anesthetized, open-chest dogs. Sixty unipolar electrograms were simultaneously recorded from the entire cardiac surface of the heart. The amplitude of ST alternans (STa) was determined as the difference in the ST-segment magnitude between 2 consecutive electrograms. We accepted the greatest STa among 60 leads for evaluation. High-dose flecainide (100 µg · kg-1 · min-1) increased STa and evoked a spontaneous VF. The STa in high-dose flecainide loading (8.7±3.4 mV; mean±SEM) was significantly greater than that in disopyramide or lidocaine (0.9±0.4 and 0.8±0.2 mV, P<0.05). Treatment of 4-aminopyridine (4-AP) suppressed the increase in STa and the occurrence of VF evoked by flecainide, while E4031 or verapamil did not inhibit those.
ConclusionsFlecainide caused the ST alternans that was closely correlated to the occurrence of VF. Because the ST alternans was suppressed by 4-AP treatment, a 4-APsensitive current such as Ito or Isus may play an important role on this phenomenon.
Key Words: flecainide arrhythmia reentry fibrillation
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