In vivo and in vitro antiarrhythmic effects of SSR149744C in animal models of atrial fibrillation and ventricular arrhythmias

被引:35
作者
Gautier, P [1 ]
Serre, M [1 ]
Cosnier-Pucheu, S [1 ]
Djandjighian, L [1 ]
Roccon, A [1 ]
Herbert, JM [1 ]
Nisato, D [1 ]
机构
[1] Sanofi Synthelabo Rech, Cardiovasc Thrombosis Dept, F-34184 Montpellier, France
关键词
amiodarone; SSR149744C; antiarrhythmic; animal model;
D O I
10.1097/01.fjc.0000151899.03379.76
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
SSR149744C (2-butyl-3-{4-[3-(dibutylamino)propyl]-benzoyl}-1-benzofuran-5-carboxylate isopropyl fumarate) is a new noniodinated benzofuran derivative structurally related to amiodarone and dronedarone that is currently undergoing clinical trials as an antiarrhythmic agent. As SSR149744C exhibits electrophysiological and hemodynamic properties of class I, II, III, and IV antiarrhythmic agents, the aim of this study was to evaluate its acute intravenous (IV) or oral (PO) antiarrhythmic activities in in vitro and in vivo animal models of atrial and ventricular arrhythmias. In vagally induced atrial fibrillation (AF) in anesthetized dogs, SSR149744C (3 and 10 mg/kg IV) terminated AF in all 7 dogs and prevented reinduction in 4 out of 7 dogs; effective refractory periods of right atrium were dose-dependently and frequency-independently lengthened. In low-K+ medium-induced AF models, SSR149744C (0.1 to 1 muM) prevented AF in isolated guinea pig hearts in a concentration-dependent manner. At the ventricular level, SSR149744C (0.1 to 10 mg/kg IV and 3 to 90 mg/kg PO) prevented reperfusion-induced arrhythmias in anesthetized rats with a dose-effect relationship, and, at doses of 30 to 90 mg/kg PO, it reduced early (0-24 hours) mortality following permanent left coronary artery ligature in conscious rats. The present results show that SSR149744C is an effective antiarrhythmic agent in atrial fibrillation and in ventricular arrhythmias. Like amiodarone and dronedarone, its efficiency in these animal models of arrhythmias is likely be related to its multifactorial mechanism of action.
引用
收藏
页码:125 / 135
页数:11
相关论文
共 43 条
[1]  
Brooks RR, 1996, P SOC EXP BIOL MED, V212, P84
[3]   I-K independent class III actions of MS-551 compared with sematilide and dofetilide during reperfusion in anaesthetized rats [J].
Chen, JG ;
Komori, S ;
Li, BH ;
Tamura, K ;
Hashimoto, K .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 119 (05) :937-942
[4]   Independent contribution of catecholamines to arrhythmogenesis during evolving infarction in the isolated rat heart [J].
Clements-Jewery, H ;
Hearse, DJ ;
Curtis, MJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2002, 135 (03) :807-815
[5]  
COSNIER S, 1999, FUND CLIN PHARM, V13, pS73
[6]  
Cosnier-Pucheu S, 2003, EUR HEART J, V2, P53
[7]  
COSNIERPUCHEU S, 2001, ARCH MAL COEUR VAISS, V94, P21
[8]  
Coumel P., 1979, CARDIAC ARRHYTHMIAS, P243
[9]   MODELS FOR THE STUDY OF ARRHYTHMIAS IN MYOCARDIAL-ISCHEMIA AND INFARCTION - THE USE OF THE RAT [J].
CURTIS, MJ ;
MACLEOD, BA ;
WALKER, MJA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1987, 19 (04) :399-419
[10]  
FABIANI JN, 1977, AM CLIN THORAC CARDI, V16, P167