Milrinone improves function in failing adult hearts, but it has not be
en examined in the immature myocardium. The purpose of this study was
to characterize the effects of milrinone, a phosphodiesterase inhibito
r, on immature hearts, and compare these to dobutamine, a commonly use
d catecholamine inotrope. One hundred isolated working neonatal rabbit
hearts were used. Hearts were made ischemic (37 degrees C) for 1 hour
and reperfused for 0, 10, 40, or 70 minutes. In separate groups, infu
sion of milrinone (1.0 mu g/mL) or dobutamine (0.1 mu g/mL) was begun
after reperfusion for 10 or 40 minutes. High energy phosphates, total
nondiffusable nucleotides, cyclic adenosine monophosphate (cAMP), and
the percent recovery of cardiac output were determined. Cardiac output
returned to normal, and adenosine triphosphate (ATP) and total nondif
fusable nucleotide levels did not decline when dobutamine or milrinone
were begun after 10 minutes of reperfusion. In hearts receiving inotr
opes after 40 minutes of reperfusion, when high energy phosphates were
low, Am increased, and total nondiffusable nucleotide repletion was o
bserved. Cardiac output did not improve when inotropes were begun afte
r 40 minutes. cAMP was higher in milrinone hearts compared to dobutami
ne, but there was no simple relation between cAMP and ventricular func
tion. Inotropes may increase purine salvage pathway activity. Deriving
maximum benefit from inotropes may depend on beginning infusions earl
y, before the appearance of irreversible changes.