Key result
Rapid ventricular pacing at 200-240 beats/min for 4-8 weeks in swine reliably produced a stable model of chronic heart failure with severe systolic dysfunction and chamber dilation.
Rapid ventricular pacing in swine provides a stable, reproducible preclinical model of chronic heart failure for testing new treatment modalities.
Supports swine rapid-pacing model for preclinical HF therapy testing; leaves open clinical translation.
A stable and reliable model of chronic heart failure is required for many experiments to understand hemodynamics or to test effects of new treatment methods. Here, we present such a model by tachycardia-induced cardiomyopathy, which can be produced by rapid cardiac pacing in swine. A single pacing lead is introduced transvenously into fully anaesthetized healthy swine, to the apex of the right ventricle, and fixated. Its other end is then tunneled dorsally to the paravertebral region. There, it is connected to an in-house modified heart pacemaker unit that is then implanted in a subcutaneous pocket. After 4 - 8 weeks of rapid ventricular pacing at rates of 200 - 240 beats/min, physical examination revealed signs of severe heart failure - tachypnea, spontaneous sinus tachycardia, and fatigue. Echocardiography and X-ray showed dilation of all heart chambers, effusions, and severe systolic dysfunction. These findings correspond well to decompensated dilated cardiomyopathy and are also preserved after the cessation of pacing. This model of tachycardia-induced cardiomyopathy can be used for studying the pathophysiology of progressive chronic heart failure, especially hemodynamic changes caused by new treatment modalities like mechanical circulatory supports. This methodology is easy to perform and the results are robust and reproducible.
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Hála et al. (2018) studied Chronic heart failure model. Rapid ventricular pacing was evaluated on Development of severe heart failure signs and systolic dysfunction. Rapid ventricular pacing at 200-240 beats/min for 4-8 weeks in swine reliably produced a stable model of chronic heart failure with severe systolic dysfunction and chamber dilation.
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