Key result
Short-term intravenous infusion of olprinone (3.0 microg/kg/min) in pigs with heart failure increased cardiac output by 40.0% (p<0.05) and decreased left atrial pressure by 35.9% (p<0.001).
Why the study?
Does olprinone improve cardiohemodynamics and plasma hormones in conscious pigs with pacing-induced heart failure?
Does olprinone improve cardiohemodynamics and plasma hormones in conscious pigs with pacing-induced heart failure?
p-value: p=<0.05
Short-term intravenous infusion of olprinone ameliorates decreased left ventricular function without affecting myocardial oxygen consumption or the sympathetic nervous system in a pig model of heart failure.
May improve hemodynamics in porcine heart failure; hypothesis-generating and leaves clinical translation open.
We examined the effects of a novel phosphodiesterase III inhibitor, olprinone, on the cardiohemodynamics and plasma hormones in conscious pigs with pacing-induced heart failure. After pacing for 5-10 days, cardiac output (CO) decreased from 2.25 +/- 0.17 to 1.67 +/- 0.13 L/min (n = 8, p < 0.01) and stroke volume (SV) decreased from 20.1 +/- 2.1 to 12.0 +/- 1.6 ml (n = 8, p < 0.01), whereas left arterial pressure (LAP) increased from 2.8 +/- 1.2 to 16.7 -/+ 0.9 mm Hg (n = 7, p < 0.001) and systemic vascular resistance (SVR) increased from 38.7 +/- 3.5 to 49.8 +/- 4.2 mm Hg/L/min (n = 8, p < 0.01). Sequential intravenous infusions of 0.03, 0.3, and 3.0 microg/kg/min of olprinone at 30-min intervals to eight pigs caused dose-dependent increases in the decreased CO, SV, and maximal rate of rise in left ventricular pressure (LV dP/dt(max)) and decreased the elevated LAP and SVR. Olprinone at 3.0 microg/kg/min maximally increased CO, SV, and LV dP/dt(max) by 40.0 +/- 10.8% (p < 0.05 vs. vehicle), 25.6 +/- 6.9% (p < 0.05), and 43.9 +/- 11.2% (p < 0.01), respectively, and brought about a slight increase in heart rate and decreases in LAP and SVR, by 35.9 +/- 7.3% (p < 0.001) and 27.9 +/- 4.8% (p < 0.01), respectively. Olprinone did not affect the rate-pressure product. In addition, olprinone produced significant decreases in the plasma levels of atrial natriuretic peptide and cyclic guanosine monophosphate, with no changes in the plasma levels of cyclic adenosine monophosphate and catecholamines or plasma renin activity. These findings indicate that the short-term intravenous infusions of olprinone ameliorated the decreased left ventricular function without affecting myocardial oxygen consumption or the sympathetic nervous system in conscious pigs with heart failure.
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Adachi et al. (1997) studied Pacing-induced heart failure (n=8). Olprinone vs. Vehicle was evaluated on Cardiohemodynamics (cardiac output, stroke volume, LV dP/dt(max), left atrial pressure, systemic vascular resistance) (p=<0.05). Short-term intravenous infusion of olprinone (3.0 microg/kg/min) in pigs with heart failure increased cardiac output by 40.0% (p<0.05) and decreased left atrial pressure by 35.9% (p<0.001).
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