Antiarrhythmic effects of JTV-519, a novel cardioprotective drug, on atrial fibrillation/flutter in a canine sterile pericarditis model

被引:60
作者
Kumagai, K [1 ]
Nakashima, H [1 ]
Gondo, N [1 ]
Saku, K [1 ]
机构
[1] Fukuoka Univ, Sch Med, Dept Cardiol, Jonan Ku, Fukuoka 8140180, Japan
关键词
atrial fibrillation; atrial flutter; ischemia; potassium channel; pharmacology;
D O I
10.1046/j.1540-8167.2003.03050.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: A new cardioprotective drug, JTV-519, blocks Na+ current and inwardly rectifying K+ current and inhibits Ca2+ current. However, its role in atrial electrophysiology is unknown. We investigated the antiarrhythmic effects of JTV-519 on atrial fibrillation/flutter in the canine sterile pericarditis model. Methods and Results: In nine dogs with sterile pericarditis, 38 episodes of sustained (>30 sec) atrial fibrillation (8 dogs) and 24 episodes of sustained atrial flutter (7 dogs) were induced by rapid atrial pacing. When atrial fibrillation or atrial flutter was sustained >15 minutes, it was cardioverted and reinduced. The inducibility of atrial fibrillation/flutter, the atrial effective refractory period, and the intra-atrial conduction time were compared before and after the continuous infusion of JTV-519 (0.03 mg/kg/min). JTV-519 significantly decreased the mean number of sustained atrial fibrillation episodes (from 4.2 +/- 2.9 to 0 0, P < 0.01). In contrast, atrial flutter was still inducible in 4 dogs after JTV-519 (from 2.7 +/- 2.5 to 1.6 +/- 2.1, P = NS). JTV-519 significantly prolonged effective refractory period (from 123 +/- 18 to 143 +/- 14 msec, from 127 +/- 18 to 151 +/- 12 msec, and from 132 +/- 13 to 159 +/- 9 msec at basic cycle lengths of 200, 300, and 400 msec, respectively, P < 0.01), but it did not affect the intra-atrial conduction time (from 47 ± 11 msec to 48 ± 11 msec, P = NS). Conclusion: JTV-519 had significant protective effects on atrial fibrillation in the canine sterile pericarditis model, mainly by increasing effective refractory period, suggesting that it may have potential as a novel antiarrhythmic agent for atrial fibrillation.
引用
收藏
页码:880 / 884
页数:5
相关论文
共 16 条
[1]  
ALLESSIE MA, 1995, CARDIAC ELECTROPHYSI, P562
[2]   FAILURE IN THE RATE ADAPTATION OF THE ATRIAL REFRACTORY PERIOD - ITS RELATIONSHIP TO VULNERABILITY [J].
ATTUEL, P ;
CHILDERS, R ;
CAUCHEMEZ, B ;
POVEDA, J ;
MUGICA, J ;
COUMEL, P .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 1982, 2 (02) :179-197
[3]   ELECTROPHYSIOLOGIC STUDIES IN ATRIAL-FIBRILLATION - SLOW CONDUCTION OF PREMATURE IMPULSES - A POSSIBLE MANIFESTATION OF THE BACKGROUND FOR REENTRY [J].
COSIO, FG ;
PALACIOS, J ;
VIDAL, JM ;
COCINA, EG ;
GOMEZSANCHEZ, MA ;
TAMARGO, L .
AMERICAN JOURNAL OF CARDIOLOGY, 1983, 51 (01) :122-130
[4]   RELATION BETWEEN ECHOCARDIOGRAPHICALLY DETERMINED LEFT ATRIAL SIZE AND ATRIAL-FIBRILLATION [J].
HENRY, WL ;
MORGANROTH, J ;
PEARLMAN, AS ;
CLARK, CE ;
REDWOOD, DR ;
ITSCOITZ, SB ;
EPSTEIN, SE .
CIRCULATION, 1976, 53 (02) :273-279
[5]   EARLY ATRIAL-FIBRILLATION DURING EVOLVING MYOCARDIAL-INFARCTION - A CONSEQUENCE OF IMPAIRED LEFT ATRIAL PERFUSION [J].
HOD, H ;
LEW, AS ;
KELTAI, M ;
CERCEK, B ;
GEFT, IL ;
SHAH, PK ;
GANZ, W .
CIRCULATION, 1987, 75 (01) :146-150
[6]   NEW 1,4-BENZOTHIAZEPINE DERIVATIVE, K201, DEMONSTRATES CARDIOPROTECTIVE EFFECTS AGAINST SUDDEN CARDIAC CELL-DEATH AND INTRACELLULAR CALCIUM BLOCKING ACTION [J].
KANEKO, N .
DRUG DEVELOPMENT RESEARCH, 1994, 33 (04) :429-438
[7]   Effects of a novel cardioprotective drug, JTV-519, on membrane currents of guinea pig ventricular myocytes [J].
Kimura, J ;
Kawahara, M ;
Sakai, E ;
Yatabe, J ;
Nakanishi, H .
JAPANESE JOURNAL OF PHARMACOLOGY, 1999, 79 (03) :275-281
[8]   ELECTROPHYSIOLOGICAL PROPERTIES IN CHRONIC LONE ATRIAL-FIBRILLATION [J].
KUMAGAI, K ;
AKIMITSU, S ;
KAWAHIRA, K ;
KAWANAMI, F ;
YAMANOUCHI, Y ;
HIROKI, T ;
ARAKAWA, K .
CIRCULATION, 1991, 84 (04) :1662-1668
[9]  
Kumagai K, 1997, CIRCULATION, V95, P511
[10]   Inhibitory effects of JTV-519, a novel cardioprotective drug, on potassium currents and experimental atrial fibrillation in guinea-pig hearts [J].
Nakaya, H ;
Furusawa, Y ;
Ogura, T ;
Tamagawa, M ;
Uemura, H .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (07) :1363-1372