New mechanism of antiarrhythmic drug action - Increasing L-type calcium current prevents reentrant ventricular tachycardia in the infarcted canine heart

被引:18
作者
Cabo, C [1 ]
Schmitt, H [1 ]
Wit, AL [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pharmacol, New York, NY 10032 USA
关键词
tachycardia; myocardial infarction; calcium; ion channels; mapping; antiarrhythmia agents;
D O I
10.1161/01.CIR.102.19.2417
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-We studied whether increasing L-type calcium current has antiarrhythmic effects. Methods and Results-Reentrant circuits in the epicardial border zone (EBZ) of healing canine infarcts were mapped during sustained ventricular tachycardia, The cardiac-specific L-type calcium current enhancer Bay Y5959 prevented initiation of sustained ventricular tachycardia in 7 of 14 experiments. Bay Y5959 caused slowing of conduction in areas of slow nonuniform conduction in reentrant circuits; block eventually occurred. Conduction was not affected in other regions of the circuits or in more normal areas of the EBZ, nor was the EBZ effective refractory period changed. Bay Y5959 also improved conduction of premature impulses so that lines of unidirectional block necessary for VT initiation were not formed, an effect not related to a change in the effective refractory period at the site of block. Conclusions-Block of conduction caused by enhanced L-type calcium current in reentrant circuits may result from a decreased gap junctional conductance consequent to an increase in intracellular calcium. An increase in L-type calcium current may improve conduction of premature impulses.
引用
收藏
页码:2417 / 2425
页数:9
相关论文
共 21 条
[1]  
Bechem M., 1997, Life Sciences, V60, P107
[2]   Mechanisms for absence of inverse relationship between coupling intervals of premature impulses initiating reentrant ventricular tachycardia and intervals between premature and first tachycardia impulses [J].
Cabo, C ;
Deruyter, B ;
Coromilas, J ;
Wit, AL .
CIRCULATION, 1997, 96 (09) :3136-3147
[3]   ELECTROPHYSIOLOGICAL EFFECTS OF FLECAINIDE ON ANISOTROPIC CONDUCTION AND REENTRY IN INFARCTED CANINE HEARTS [J].
COROMILAS, J ;
SALTMAN, AE ;
WALDECKER, B ;
DILLON, SM ;
WIT, AL .
CIRCULATION, 1995, 91 (08) :2245-2263
[4]   A MODEL FOR EARLY AFTERDEPOLARIZATIONS - INDUCTION WITH THE CA-2+ CHANNEL AGONIST BAY-K-8644 [J].
JANUARY, CT ;
RIDDLE, JM ;
SALATA, JJ .
CIRCULATION RESEARCH, 1988, 62 (03) :563-571
[5]  
KATOH H, 1990, J PHARMACOL EXP THER, V253, P1077
[6]   CELL PAIRS ISOLATED FROM ADULT GUINEA-PIG AND RAT HEARTS - EFFECTS OF [CA-2+]I ON NEXAL MEMBRANE RESISTANCE [J].
MAURER, P ;
WEINGART, R .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1987, 409 (4-5) :394-402
[7]   DEPENDENCE OF JUNCTIONAL CONDUCTANCE ON PROTON, CALCIUM AND MAGNESIUM-IONS IN CARDIAC PAIRED CELLS OF GUINEA-PIG [J].
NOMA, A ;
TSUBOI, N .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 382 :193-&
[8]  
Peters NS, 1997, CIRCULATION, V95, P988
[9]   Effects of Bay Y5959 on Ca2+ currents and intracellular Ca2+ in cells that have survived in the epicardial border of the infarcted canine heart [J].
Pu, JL ;
Ruffy, F ;
Boyden, PA .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1999, 33 (06) :929-937
[10]   Alterations of Na+ currents in myocytes from epicardial border zone of the infarcted heart - A possible ionic mechanism for reduced excitability and postrepolarization refractoriness [J].
Pu, JL ;
Boyden, PA .
CIRCULATION RESEARCH, 1997, 81 (01) :110-119