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
[21]   Phenotypic screening for heart rate variability in the mouse [J].
Gehrmann, J ;
Hammer, PE ;
Maguire, CT ;
Wakimoto, H ;
Triedman, JK ;
Berul, CI .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 279 (02) :H733-H740
[22]   VALUE OF PROGRAMMED ELECTRICAL-STIMULATION USING A STANDARDIZED VENTRICULAR STIMULATION PROTOCOL IN HYPERTROPHIC CARDIOMYOPATHY [J].
GEIBEL, A ;
BRUGADA, P ;
ZEHENDER, M ;
STEVENSON, W ;
WALDECKER, B ;
WELLENS, HJJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1987, 60 (08) :738-739
[23]   Functional consequences of elimination of Ito,f and Ito,s -: Early afterdepolarizations, atrioventricular block, and ventricular arrhythmias in mice lacking Kv1.4 and expressing a dominant-negative Kv4 α subunit [J].
Guo, WN ;
Li, HI ;
London, B ;
Nerbonne, JM .
CIRCULATION RESEARCH, 2000, 87 (01) :73-79
[24]   Inducible polymorphic ventricular tachyarrhythmias in a transgenic mouse model with a long Q-T phenotype [J].
Jeron, A ;
Mitchell, GF ;
Zhou, J ;
Murata, M ;
London, B ;
Buckett, P ;
Wiviott, SD ;
Koren, G .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (06) :H1891-H1898
[25]  
Josephson ME, 1999, J AM COLL CARDIOL, V33, P1971
[26]   Risk assessment of patients having congenital heart disease using electrophysiologic testing: Finally, opening the right door ... or, an impossible chore? [J].
Kanter, RJ .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1999, 10 (08) :1045-1048
[27]   Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient mice [J].
Kirchhoff, S ;
Nelles, E ;
Hagendorff, A ;
Krüger, O ;
Traub, O ;
Willecke, K .
CURRENT BIOLOGY, 1998, 8 (05) :299-302
[28]   In-vivo electrophysiological study in mice with chronic anterior myocardial infarction [J].
Korte, T ;
Fuchs, M ;
Guener, Z ;
von Bonin, J ;
de Sousa, M ;
Niehaus, M ;
Tebbenjohanns, J ;
Drexler, H .
JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY, 2002, 6 (02) :121-132
[29]   PROGRAMMED ELECTRICAL-STIMULATION IN HYPERTROPHIC CARDIOMYOPATHY - RESULTS IN PATIENTS WITH AND WITHOUT CARDIAC-ARREST OR SYNCOPE [J].
KUCK, KH ;
KUNZE, KP ;
SCHLUTER, M ;
NIENABER, CA ;
COSTARD, A .
EUROPEAN HEART JOURNAL, 1988, 9 (02) :177-185
[30]   A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of Ito and confers susceptibility to ventricular tachycardia [J].
Kuo, HC ;
Cheng, CF ;
Clark, RB ;
Lin, JJC ;
Lin, JLC ;
Hoshijima, M ;
Nguyêñ-Trân, VTB ;
Gu, YS ;
Ikeda, Y ;
Chu, PH ;
Ross, J ;
Giles, WR ;
Chien, KR .
CELL, 2001, 107 (06) :801-813