Mathematical analysis of canine atrial action potentials: rate, regional factors, and electrical remodeling

被引:137
作者
Ramirez, RJ
Nattel, S
Courtemanche, M
机构
[1] Montreal Heart Inst, Res Ctr, Montreal, PQ H1T 1C8, Canada
[2] McGill Univ, Dept Pharmacol, Montreal, PQ H3G 1Y6, Canada
[3] Univ Montreal, Inst Genie Biomed, Montreal, PQ H3C 3J7, Canada
[4] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[5] Univ Montreal, Dept Physiol, Montreal, PQ H3C 3J7, Canada
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2000年 / 279卷 / 04期
关键词
action potential duration; atrial fibrillation; ion channels; rate adaptation; regional heterogeneity; mathematical model;
D O I
10.1152/ajpheart.2000.279.4.H1767
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dogs have been used extensively to study atrial arrhythmias, but there are no published mathematical models of the canine atrial action potential (AP). To obtain insights into the ionic mechanisms governing canine atrial AP properties, we incorporated formulations of K+, Na+, Ca2+, and Cl- currents, based on measurements in canine atrial myocytes, into a mathematical model of the AP. The rate-dependent behavior of model APs corresponded to experimental measurements and pointed to a central role for L-type Ca2+ current inactivation in rate adaptation. Incorporating previously described regional ionic current variations into the model largely reproduced AP forms characteristic of the corresponding right atrial regions (appendage, pectinate muscle, crista terminalis, and atrioventricular ring). When ionic alterations induced by tachycardia-dependent remodeling were incorporated, the model reproduced qualitatively the AP features constituting the cellular substrate for atrial fibrillation. We conclude that this ionic model of the canine atrial AP agrees well with experimental measurements and gives potential insights into mechanisms underlying functionally important electrophysiological phenomena in canine atrium.
引用
收藏
页码:H1767 / H1785
页数:19
相关论文
共 41 条
[1]   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
[2]   INHOMOGENEITY OF CELLULAR REFRACTORINESS IN HUMAN ATRIUM - FACTOR OF ARRHYTHMIA [J].
BOUTJDIR, M ;
LEHEUZEY, JY ;
LAVERGNE, T ;
CHAUVAUD, S ;
GUIZE, L ;
CARPENTIER, A ;
PERONNEAU, P .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 1986, 9 (06) :1095-1100
[3]   THE EFFECTS ON ATRIAL ELECTROPHYSIOLOGY AND STRUCTURE OF SURGICALLY INDUCED RIGHT ATRIAL ENLARGEMENT IN DOGS [J].
BOYDEN, PA ;
HOFFMAN, BF .
CIRCULATION RESEARCH, 1981, 49 (06) :1319-1331
[4]   EFFECTS OF LEFT ATRIAL ENLARGEMENT ON ATRIAL TRANSMEMBRANE POTENTIALS AND STRUCTURE IN DOGS WITH MITRAL-VALVE FIBROSIS [J].
BOYDEN, PA ;
TILLEY, LP ;
PHAM, TD ;
LIU, SK ;
FENOGLIO, JJ ;
WIT, AL .
AMERICAN JOURNAL OF CARDIOLOGY, 1982, 49 (08) :1896-1908
[5]   Unitary Cl- channels activated by cytoplasmic Ca2+ in canine ventricular myocytes [J].
Collier, ML ;
Levesque, PC ;
Kenyon, JL ;
Hume, JR .
CIRCULATION RESEARCH, 1996, 78 (05) :936-944
[6]   Ionic targets for drug therapy and atrial fibrillation-induced electrical remodeling: insights from a mathematical model [J].
Courtemanche, M ;
Ramirez, RJ ;
Nattel, S .
CARDIOVASCULAR RESEARCH, 1999, 42 (02) :477-489
[7]   Ionic mechanisms underlying human atrial action potential properties: insights from a mathematical model [J].
Courtemanche, M ;
Ramirez, RJ ;
Nattel, S .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 275 (01) :H301-H321
[8]   A MATHEMATICAL-MODEL OF A RABBIT SINOATRIAL NODE CELL [J].
DEMIR, SS ;
CLARK, JW ;
MURPHEY, CR ;
GILES, WR .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (03) :C832-C852
[9]   FAST SODIUM CURRENT IN CARDIAC-MUSCLE - A QUANTITATIVE DESCRIPTION [J].
EBIHARA, L ;
JOHNSON, EA .
BIOPHYSICAL JOURNAL, 1980, 32 (02) :779-790
[10]   Importance of refractoriness heterogeneity in the enhanced vulnerability to atrial fibrillation induction caused by tachycardia-induced atrial electrical remodeling [J].
Fareh, S ;
Villemaire, C ;
Nattel, S .
CIRCULATION, 1998, 98 (20) :2202-2209