Key result
Milrinone and levosimendan did not alter microdialysate-measured metabolic parameters or calcium overload during acute myocardial ischaemia in pigs compared to placebo.
Why the study?
Does milrinone or levosimendan alter calcium overload and myocardial metabolism in a porcine model of acute myocardial ischemia?
RCT (n=20)
randomised
Does milrinone or levosimendan alter calcium overload and myocardial metabolism in a porcine model of acute myocardial ischemia?
In a porcine model of acute myocardial ischemia, milrinone and levosimendan did not alter calcium overload or metabolic parameters, indicating neither an energy-conserving effect nor a worsening of metabolism.
No metabolic effects in porcine ischemia model; leaves open translation to human acute MI.
BACKGROUND: Although inotropic stimulation is considered harmful in the presence of myocardial ischaemia, both calcium sensitisers and phosphodiesterase inhibitors may offer cardioprotection. We hypothesise that these cardioprotective effects are related to an acute alteration of myocardial metabolism. We studied in vivo effects of milrinone and levosimendan on calcium overload and ischaemic markers using left ventricular microdialysis in pigs with acute myocardial ischaemia. METHODS: Anaesthetised juvenile pigs, average weight 36 kg, were randomised to one of three intravenous treatment groups: milrinone 50 μg/kg bolus plus infusion 0.5 μg/kg/min (n = 7), levosimendan 24 μg/kg plus infusion 0.2 μg/kg/min (n = 7), or placebo (n = 6) for 60 min prior to and during a 45 min acute regional coronary occlusion. Systemic and myocardial haemodynamics were assessed, and microdialysis was performed with catheters positioned in the left ventricular wall. (45) Ca(2+) was included in the microperfusate in order to assess local calcium uptake into myocardial cells. The microdialysate was analysed for glucose, lactate, pyruvate, glycerol, and for (45) Ca(2+) recovery. RESULTS: During ischaemia, there were no differences in microdialysate-measured parameters between control animals and milrinone- or levosimendan-treated groups. In the pre-ischaemic period, arterial blood pressure decreased in all groups while myocardial oxygen consumption remained stable. CONCLUSIONS: These findings reject the hypothesis of an immediate energy-conserving effect of milrinone and levosimendan during acute myocardial ischaemia. On the other hand, the data show that inotropic support with milrinone and levosimendan does not worsen the metabolic parameters that were measured in the ischaemic myocardium.
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Axelsson et al. (2013) conducted an RCT in acute myocardial ischaemia (n=20). Milrinone and levosimendan vs. placebo was evaluated on microdialysate-measured parameters (glucose, lactate, pyruvate, glycerol, and 45Ca2+ recovery). Milrinone and levosimendan did not alter microdialysate-measured metabolic parameters or calcium overload during acute myocardial ischaemia in pigs compared to placebo.
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