Myocardial infarction in rodents induced alterations in heart rhythm dynamics consistent with sympathoexcitation and parasympathetic withdrawal, including a >50% reduction in RR interval variation in heterozygous mice.
Does myocardial infarction alter heart rate variability in experimental rodent models?
Experimental rodent models of myocardial infarction recapitulate HRV dynamics observed in humans, highlighting the importance of mouse strain when evaluating autonomic function.
The analysis of beating rate provides information on the modulatory action of the autonomic nervous system on the heart, which mediates adjustments of cardiac function to meet hemodynamic requirements. In patients with myocardial infarction, alterations of heart rate variability (HRV) have been correlated to the occurrence of arrhythmic events and all-cause mortality. In the current study, we tested whether experimental rodent models of myocardial infarction recapitulate dynamics of heart rate variability observed in humans, and constitute valid platforms for understanding mechanisms linking autonomic function to the development and manifestation of cardiovascular conditions. For this purpose, HRV was evaluated in two engineered mouse lines using electrocardiograms collected in the conscious, restrained state, using a tunnel device. Measurements were obtained in naïve mice and animals at 3–∼28 days following myocardial infarction, induced by permanent coronary artery ligation. Two mouse lines with inbred and hybrid genetic background and, respectively, homozygous (Homo) and heterozygous (Het) for the MerCreMer transgene, were employed. In the naïve state, Het female and male mice presented prolonged RR interval duration (∼9%) and a ∼4-fold increased short- and long-term RR interval variability, with respect to sex-matched Homo mice. These differences were abrogated by pharmacological interventions inhibiting the sympathetic and parasympathetic axes. At 3–∼14 days after myocardial infarction, RR interval duration increased in Homo mice, but was not affected in Het animals. In contrast, Homo mice had minor modifications in HRV parameters, whereas substantial ( 50%) reduction of short- and long-term RR interval variation occurred in Het mice. Interestingly, ex vivo studies in isolated organs documented that intrinsic RR interval duration increased in infarcted vs. non-infarcted Homo and Het hearts, whereas RR interval variation was not affected. In conclusion, our study documents that, as observed in humans, myocardial infarction in rodents is associated with alterations in heart rhythm dynamics consistent with sympathoexcitation and parasympathetic withdrawal. Moreover, we report that mouse strain is an important variable when evaluating autonomic function via the analysis of HRV.
Pizzo et al. (Mon,) conducted a other in Myocardial infarction. Myocardial infarction (coronary artery ligation) vs. Naïve state (pre-infarction) was evaluated on Heart rate variability (short- and long-term RR interval variation). Myocardial infarction in rodents induced alterations in heart rhythm dynamics consistent with sympathoexcitation and parasympathetic withdrawal, including a >50% reduction in RR interval variation in heterozygous mice.