- Milrinone
- Phosphodiesterase Inhibition → prevents removal (hydrolysis of) cGMP in the smooth musculature → vasodilation in both arteries and veins
- Phosphodiesterase is an enzyme that hydrolyzes the second messenger cyclic adenosine monophosphate(cAMP) and guanosine monophosphate(cGMP), terminating their effects
- Vasodilatory effects of milrinone are more potent than beta-2 agonists, including dobutamine and isoproterenol.
- Indication
- Intraarterial followed by systemic milrinone for 14 days demonstrated a significant enlargement in diameter of vasospastic intracranial arteries. The systemic dose started at 50 μg/kg/min and was titrated to 1.5 μg/kg/min.
- Pharmacokinetics
- Plasma half-life: 2 to 2.5 hours.
- Metabolism: liver
- Excretion: urine
Phosphodiesterase inhibitor
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