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Vol. 282, Issue 1, 23-31, 1997
Cardiology Section, Bowman Gray School of Medicine of Wake Forest
University, Winston-Salem, North Carolina
We compared the effects of pimobendan (0.25 mg/kg i.v.), a
Ca++ sensitizer, with some phosphodiesterase-III inhibition
effects, and amrinone (1 mg/kg plus 10 µg/kg/min i.v.), a PDE-III
inhibitor, on left ventricular (LV) systolic and diastolic performance,
both at rest and during exercise, in seven conscious dogs before and after pacing-induced congestive heart failure (CHF). Before CHF, under
resting conditions, both pimobendan and amrinone caused a similar
significant decrease in left ventricle size and end-systolic pressure,
arterial elastance, and the time constant of LV relaxation. Similar
results were obtained during exercise. Both agents also produced a
similar increase in EES, the slope of the LV
end-systolic pressure-volume relation (3.4 ± 1.5 vs.
4.2 ± 1.1 mm Hg/ml; amrinone vs. pimobendan). After
CHF, the vasodilatory effects of amrinone and pimobendan were preserved
both at rest and during exercise; however, the inotropic actions were
different. After CHF, pimobendan increased EES
(3.9 ± 0.5 vs. 5.7 ± 0.4 mm Hg/ml, P < .05), decreased the time constant of LV relaxation, increased the
maximum rate of LV filling (37 ± 19 ml/sec) (P < .05) and
produced a downward shift of the early diastolic portion of LV
pressure-volume loop. Pimobendan also augmented LV contractile
performance during CHF exercise. In contrast, after CHF, amrinone no
longer produced a positive inotropic effect. Amrinone improved LV
relaxation and filling, both at rest and during exercise after CHF, but
significantly less than pimobendan. We conclude that after CHF, the
cardiac response to a PDE-III inhibitor is attenuated, but the response to Ca++ sensitizer is preserved. Thus, after CHF,
pimobendan is more effective than amrinone in enhancing LV contractile
state, LV relaxation and LV filling both at rest and during exercise.