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Department of Medicine and Division of Physiology, Schools of Medicine and Public Health, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21287
The mouse is the species of choice for
creating genetically engineered models of human disease. To study
detailed systolic and diastolic left ventricular (LV) chamber mechanics
in mice in vivo, we developed a miniaturized conductance-manometer
system.
-Chloralose-urethan-anesthetized animals were instrumented
with a two-electrode pressure-volume catheter advanced via the LV apex to the aortic root. Custom electronics provided time-varying
conductances related to cavity volume. Baseline hemodynamics were
similar to values in conscious animals: 634 ± 14 beats/min, 112 ± 4 mmHg, 5.3 ± 0.8 mmHg, and 11,777 ± 732 mmHg/s for heart
rate, end-systolic and end-diastolic pressures, and
maximum first derivative of ventricular pressure with respect to time
(dP/dtmax),
respectively. Catheter stroke volume during preload reduction by
inferior vena caval occlusion correlated with that by ultrasound aortic
flow probe (r2 = 0.98). This maneuver yielded end-systolic elastances of 79 ± 21 mmHg/µl, preload-recruitable stroke work of 82 ± 5.6 mmHg, and
slope of
dP/dtmax-end-diastolic
volume relation of 699 ± 100 mmHg · s
1 · µl
1,
and these relations varied predictably with acute inotropic interventions. The control normalized time-varying elastance curve was
similar to human data, further supporting comparable chamber mechanics
between species. This novel approach should greatly help assess
cardiovascular function in the blood-perfused murine heart.
mouse; ventricular function; hemodynamics; conductance volumetry
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