Myocytes from dogs with pacing-induced heart failure exhibited significantly prolonged action potential duration (1097 +/- 73 ms vs 842 +/- 56 ms; P < .05) and reduced transient outward K+ current.
In a canine model of pacing-induced heart failure, downregulation of the transient outward potassium current (Ito) contributes to action potential prolongation, providing a mechanistic model for repolarization abnormalities and sudden death risk in human heart failure.
Absolute Event Rate: 1097% vs 842%
p-value: p=<.05
Membrane current abnormalities have been described in human heart failure. To determine whether similar current changes are observed in a large animal model of heart failure, we studied dogs with pacing-induced cardiomyopathy. Myocytes isolated from the midmyocardium of 13 dogs with heart failure induced by 3 to 4 weeks of rapid ventricular pacing and from 16 nonpaced control dogs did not differ in cell surface area or resting membrane potential. Nevertheless, action potential duration (APD) was significantly prolonged in myocytes isolated from failing ventricles (APD at 90% repolarization, 1097 +/- 73 milliseconds failing hearts, n = 30 versus 842 +/- 56 milliseconds control hearts, n = 25; P < .05), and the prominent repolarizing notch in phase 1 was dramatically attenuated. Basal L-type Ca2+ current and whole-cell Na+ current did not differ in cells from failing and from control hearts, but significant differences in K+ currents were observed. The density of the inward rectifier K+ current (IKl) was reduced in cells from failing hearts at test potentials below -90 mV (at -150 mV, -19.1 +/- 2.2 pA/pF failing hearts, n = 18 versus -32.2 +/- 5.1 pA/pF control hearts, n = 15; P < .05). The small outward current component of IKl was also reduced in cells from failing hearts (at -60 mV, 1.7 +/- 0.2 pA/pF failing hearts versus 2.5 +/- 0.2 pA/pF control hearts; P < .05). The peak of the Ca(2+)-independent transient outward current (Ito) was dramatically reduced in myocytes isolated from failing hearts compared with nonfailing control hearts (at +80 mV, 7.0 +/- 0.9 pA/pF failing hearts, n = 20 versus 20.4 +/- 3.2 pA/pF control hearts, n = 15; P < .001), while the steady state component was unchanged. There were no significant differences in Ito kinetics or single-channel conductance. A reduction in the number of functional Ito channels was demonstrated by nonstationary fluctuation analysis (0.4 +/- 0.03 channels per square micrometer failing hearts, n = 5 versus 1.2 +/- 0.1 channels per square micrometer control hearts, n = 3; P < .001). Pharmacological reduction of Ito by 4-aminopyridine in control myocytes decreased the notch amplitude and prolonged the APD. Current clamp-release experiments in which current was injected for 8 milliseconds to reproduce the notch sufficed to shorten the APD significantly in cells from failing hearts. These data support the hypothesis that downregulation of Ito in pacing-induced heart failure is at least partially responsible for the action potential prolongation. Because the repolarization abnormalities mimic those in cells isolated from failing human ventricular myocardium, canine pacing-induced cardiomyopathy may provide insights into the development of repolarization abnormalities and the mechanisms of sudden death in patients with heart failure.
Kääb et al. (1996) studied Pacing-induced heart failure (n=29). Rapid ventricular pacing vs. Nonpaced control was evaluated on Action potential duration (APD) at 90% repolarization (p=<.05). Myocytes from dogs with pacing-induced heart failure exhibited significantly prolonged action potential duration (1097 +/- 73 ms vs 842 +/- 56 ms; P < .05) and reduced transient outward K+ current.