Implications of ventricular arrhythmia vulnerability during murine electrophysiology studies

被引:46
作者
Maguire, CT
Wakimoto, H
Patel, VV
Hammer, PE
Gauvreau, K
Berul, CI
机构
[1] Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[3] Univ Penn, Mol Cardiol Res Ctr, Philadelphia, PA 19104 USA
[4] Univ Penn, Sect Cardiac Electrophysiol, Philadelphia, PA 19104 USA
关键词
mice; ventricular tachycardia; programmed stimulation; genetics;
D O I
10.1152/physiolgenomics.00034.2003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Programmed ventricular stimulation is being performed for the provocation of ventricular arrhythmias in genetically engineered mice. Despite the high level of interest in this area of translational research, little attention has been given to differentiating between selectivity and specificity of induced ventricular tachycardia (VT) in phenotypically normal mice. We aimed to assess factors that may enhance inducibility of VT in wild-type (WT) mice. In vivo intracardiac electrophysiological studies (EPS) were performed in 230 WT mice of 4 strains. An octapolar electrode catheter was inserted into a jugular vein and advanced to the right atrium and ventricle. Baseline ventricular conduction, refractoriness, and arrhythmia inducibility were assessed using programmed electrical stimulation ( PES) and burst pacing. We found that nonsustained VT ( greater than or equal to 4 beats) was inducible in 68/230 (30%) mice. Duration of VT was 1.6 +/- 2.4 s, and the longest episode lasted 24 s. VT inducibility differed by strain and age. Ventricular effective refractory period ( VERP) was shorter in mice with inducible VT ( 44 +/- 12 ms) compared with noninducible mice ( 61 +/- 16 ms, P < 0.001). VERP increased with age ( P < 0.001), albeit with strain-related variability. We conclude that nonsustained VT in WT mice is reproducibly inducible and common. Genetic background variability may predispose certain strains to a higher incidence of arrhythmia induction. EPS methods impact prevalence and specificity of inducible VT. Increased VT inducibility was seen with shorter coupling intervals and application of tightly coupled extrastimuli techniques. These factors should be carefully considered when analyzing PES and burst pacing data in murine models to minimize false positives and optimize accuracy.
引用
收藏
页码:84 / 91
页数:8
相关论文
共 47 条
[1]   Value of programmed ventricular stimulation in patients with congenital heart disease [J].
Alexander, ME ;
Walsh, EP ;
Saul, JP ;
Epstein, MR ;
Triedman, JK .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1999, 10 (08) :1033-1044
[2]   Ventricular arrhythmias: When to worry [J].
Alexander, ME ;
Berul, CI .
PEDIATRIC CARDIOLOGY, 2000, 21 (06) :532-541
[3]   Idiopathic dilated cardiomyopathy in children: Prognostic indicators and outcome [J].
Arola, A ;
Tuominen, J ;
Ruuskanen, O ;
Jokinen, E .
PEDIATRICS, 1998, 101 (03) :369-376
[4]   Enhanced dispersion of repolarization and refractoriness in transgenic mouse hearts promotes reentrant ventricular tachycardia [J].
Baker, LC ;
London, B ;
Choi, BR ;
Koren, G ;
Salama, G .
CIRCULATION RESEARCH, 2000, 86 (04) :396-407
[5]   Electrophysiological abnormalities and arrhythmias in alpha MHC mutant familial hypertrophic cardiomyopathy mice [J].
Berul, CI ;
Christe, ME ;
Aronovitz, MJ ;
Seidman, CE ;
Seidman, JG ;
Mendelsohn, ME .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (04) :570-576
[6]   In vivo cardiac electrophysiology studies in the mouse [J].
Berul, CI ;
Aronovitz, MJ ;
Wang, PJ ;
Mendelsohn, ME .
CIRCULATION, 1996, 94 (10) :2641-2648
[7]   Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant myosin-binding protein C gene [J].
Berul, CI ;
McConnell, RK ;
Wakimoto, H ;
Moskowitz, IPG ;
Maguire, CT ;
Semsarian, C ;
Vargas, MM ;
Gehrmann, J ;
Seidman, CE ;
Seidman, JG .
CIRCULATION, 2001, 104 (22) :2734-2739
[8]  
Berul CI, 1998, J INTERV CARD ELECTR, V2, P7
[9]  
BERUL CI, 2001, CARDIOVASCULAR PHYSL, P237
[10]   A targeted disruption in connexin40 leads to distinct atrioventricular conduction defects [J].
Bevilacqua, LM ;
Simon, AM ;
Maguire, CT ;
Gehrmann, J ;
Wakimoto, H ;
Paul, DL ;
Berul, CI .
JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY, 2000, 4 (03) :459-467