Sodium channel-blocking properties of flecainide, a class IC antiarrhythmic drug, in guinea-pig papillary muscles An open channel blocker or an inactivated channel blocker-Reference-Cited by-同舟云学术

Sodium channel-blocking properties of flecainide, a class IC antiarrhythmic drug, in guinea-pig papillary muscles An open channel blocker or an inactivated channel blocker

Published:1989-04 Issue:4 Volume:339 Page:441-447
ISSN:0028-1298
Container-title:Naunyn-Schmiedeberg's Archives of Pharmacology
language:en
Short-container-title:Naunyn-Schmiedeberg's Arch. Pharmacol.

Author:

Kojima Michio,Hamamoto Takuyuki,Ban Takashi

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00736059.pdf

Reference39 articles.

1. Bean BP, Cohen CJ, Tsien RW (1983) Lidocaine block of cardiac sodium channels. J Gen Physiol 81:613?642

2. Bigger JT (1984) Symposium on flecainide acetate. Am J Cardiol 53:1B-122B

3. Borchard U, Boisten M (1982) Effect of flecainide on action potentials and alternating current-induced arrhythmias in mammalian myocardium. J Cardiovasc Pharmacol 4:205?212

4. Campbell TJ (1983) Importance of physico-chemical properties in determining the kinetics of the effects of class I antiarrhythmic drugs on maximum rate of depolarization in guinea-pig ventricle. Br J Pharmacol 80:33?40

5. Campbell TJ, Vaughan Williams EM (1983) Voltage- and time-dependent depression of maximum rate of depolarisation of guinea-pig ventricular action potentials by two new anti-arrhythmic drugs, flecainide and fecainide. Cardiovasc Res 17:251?258

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