We developed a technology for heart rate (HR) variability (HRV) analysis in
the mouse for characterization of HR dynamics, modulated by vagal and symp
athetic activity. The mouse is the principal animal model for studying biol
ogical processes. Mouse strains are now available harboring gene mutations
providing fundamental insights into molecular mechanisms underlying cardiac
electrical diseases. Future progress depends on enhanced understanding of
these fundamental mechanisms and the implementation of methods for the func
tional analysis of mouse cardiovascular physiology. By telemetric technique
s, standard time and frequency-domain measures of HRV were computed with an
d without autonomic blockade, and baroreflex sensitivity testing was perfor
med. HR modulation in the high-frequency component is predominantly mediate
d by the parasympathetic nervous system, whereas the low-frequency componen
t is under the influence of both the parasympathetic and sympathetic system
s. The presented technology and protocol allow for assessment of autonomic
regulation of the murine HR. Phenotypic screening for HR regulation in mice
will further enhance the value of the mouse as a model of heritable electr
ophysiological human disease.