TableEdit

Jeron, A, Mitchell, GF, Zhou, J, Murata, M, London, B, Buckett, P, Wiviott, SD and Koren, G (2000) Inducible polymorphic ventricular tachyarrhythmias in a transgenic mouse model with a long Q-T phenotype. Am. J. Physiol. Heart Circ. Physiol. 278:H1891-8

We created a mouse model with a prolonged Q-T interval and spontaneous arrhythmias by overexpressing the NH(2) terminus and first transmembrane segment (Kv1.1N206Tag) of a delayed rectifier potassium channel (LQT(+/-) mouse). Analyses were performed using whole cell recordings of cardiac myocytes, surface electrocardiography, and programmed electrical stimulation. Action potential duration (APD) was prolonged to the same extent and was more highly variable in myocytes derived from LQT(+/-) and LQT(+/+) mice than in myocytes derived from wild-type (WT) FVB mice. Under ketamine anesthesia, the Q-T interval of both LQT(+/+) and LQT(+/-) mice was comparably prolonged versus that of WT mice. Stimulation of the right ventricle using an intracardiac catheter induced polymorphic ventricular tachyarrhythmias in 50% of the LQT(+/-) mice and 36% of the LQT(+/+) mice, whereas polymorphic ventricular tachyarrhythmias were not inducible in WT mice. The analyses of LQT(+/-) and LQT(+/+) mice indicate that prolongation of the Q-T interval in LQT mice is associated with prolonged APD, increased dispersion of APD among cardiocytes, and inducibility of polymorphic ventricular tachycardia, providing the substrate for spontaneous arrhythmias in these animals.

PubMed

Action Potentials; Animals; Cardiac Pacing, Artificial; Electrocardiography; Electrophysiology; Long QT Syndrome/genetics; Mice; Mice, Transgenic/genetics; Phenotype; Reaction Time; Reference Values; Tachycardia, Ventricular/etiology; Tachycardia, Ventricular/genetics; Tachycardia, Ventricular/physiopathology