A model of myocardial ischemia for the simultaneous assessment of electrophysiological changes and arrhythmias in intact rabbits

被引:14
作者
Barrett, TD [1 ]
MacLeod, BA [1 ]
Walker, MJA [1 ]
机构
[1] UNIV BRITISH COLUMBIA, FAC MED, DEPT PHARMACOL & THERAPEUT, VANCOUVER, BC V6T 1Z3, CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
myocardial ischemia; monophasic action potentials (MAPs); arrhythmias; rabbit;
D O I
10.1016/S1056-8719(96)00145-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A method of recording epicardial monophasic action potentials (MAPs) and ischemia-induced arrhythmias following coronary artery ligation in intact rabbits is described. It is expected that this model will have utility in analyzing drug effects and mechanisms of ischemic arrhythmogenesis. Rabbits were found to have two arrhythmic phases following coronary artery occlusion which correspond to phase Ia and Ib arrhythmias in other species. Epicardial MAPs recorded from ischemic tissue allowed electrophysiological effects to be correlated with these phases. Phase Ia arrhythmias occurred within the first 2 min of coronary artery occlusion and were associated with a reduction in the maximum upstroke velocity of MAPs and changes in MAP duration, including the occurrence of alternans in duration. Phase Ib arrhythmias occurred between 8 and 15 min after coronary artery occlusion. These arrhythmias were associated with a decrease in MAP duration and amplitude, alternans in MAP duration as well as conduction block. Coronary artery occlusion reliably induced arrhythmias in rabbits if the left branch of the coronary artery and the left anterior descending artery were occluded. There was a 95% incidence of premature ventricular contractions, 35% of ventricular tachycardia, and 48% of ventricular fibrillation (n = 21). The results of this study show that epicardial MAPs can be used to aid in the characterization of the electrophysiological mechanisms of ischemia-induced arrhythmias in vivo. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:27 / 36
页数:10
相关论文
共 29 条
[1]   RELATIONSHIP OF ALTERNANS OF MONOPHASIC ACTION-POTENTIAL AND CONDUCTION DELAY INSIDE THE ISCHEMIC BORDER ZONE TO SERIOUS VENTRICULAR ARRHYTHMIA DURING ACUTE MYOCARDIAL ISCHEMIA IN DOGS [J].
ABE, S ;
NAGAMOTO, Y ;
FUKUCHI, Y ;
HAYAKAWA, T ;
KUROIWA, A .
AMERICAN HEART JOURNAL, 1989, 117 (06) :1223-1233
[2]   AN IN-VITRO METHOD FOR THE EVALUATION OF ANTIARRHYTHMIC AND ANTIISCHEMIC AGENTS BY USING PROGRAMMED ELECTRICAL-STIMULATION OF RABBIT HEART [J].
BELLEMINBAURREAU, J ;
POIZOT, A ;
HICKS, PE ;
ARMSTRONG, JM .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1994, 31 (01) :31-40
[3]   ANESTHETIZED RABBIT AS A MODEL FOR ISCHEMIA-INDUCED AND REPERFUSION-INDUCED ARRHYTHMIAS - EFFECTS OF QUINIDINE AND BRETYLIUM [J].
COKER, SJ .
JOURNAL OF PHARMACOLOGICAL METHODS, 1989, 21 (04) :263-279
[4]   ELECTROPHYSIOLOGY OF HUMAN CARDIAC-CELLS [J].
CORABOEUF, E ;
NARGEOT, J .
CARDIOVASCULAR RESEARCH, 1993, 27 (10) :1713-1725
[5]   QUANTIFICATION OF ARRHYTHMIAS USING SCORING SYSTEMS - AN EXAMINATION OF 7 SCORES IN AN INVIVO MODEL OF REGIONAL MYOCARDIAL ISCHEMIA [J].
CURTIS, MJ ;
WALKER, MJA .
CARDIOVASCULAR RESEARCH, 1988, 22 (09) :656-665
[6]   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
[7]  
DICKENSON DR, 1994, J MOL CELL CARDIOL, V26, pR169
[8]   ELECTROPHYSIOLOGICAL ALTERNANS AND RESTITUTION DURING ACUTE REGIONAL ISCHEMIA IN MYOCARDIUM OF ANESTHETIZED PIG [J].
DILLY, SG ;
LAB, MJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 402 :315-333
[9]   EFFECT OF ACUTE CORONARY-ARTERY OCCLUSION ON SUB-EPICARDIAL TRANSMEMBRANE POTENTIALS IN INTACT PORCINE HEART [J].
DOWNAR, E ;
JANSE, MJ ;
DURRER, D .
CIRCULATION, 1977, 56 (02) :217-224
[10]   METHOD AND THEORY OF MONOPHASIC ACTION-POTENTIAL RECORDING [J].
FRANZ, MR .
PROGRESS IN CARDIOVASCULAR DISEASES, 1991, 33 (06) :347-368