Key result
Isradipine increases cardiac index and lowers pressure-rate product in preclinical healed MI.
Why the study?
The effects of isradipine on hemodynamic parameters and ventricular tachycardia in chronic myocardial infarction were investigated in a preclinical model.
Does isradipine improve hemodynamics and reduce ventricular tachycardia inducibility in a pig model of healed myocardial infarction?
Does isradipine improve hemodynamics and reduce ventricular tachycardia inducibility in a pig model of healed myocardial infarction?
p-value: p=<0.02
In a pig model of healed myocardial infarction, isradipine improved hemodynamics and reduced the inducibility of ventricular tachycardia.
May improve post-MI hemodynamics in pigs; hypothesis-generating and leaves open human translation.
The calcium-entry blocker isradipine was tested in a closed-chest pig model for chronic myocardial infarction. Ischemia was evoked in anesthetized pigs (25-35 kg) by inflating a catheter balloon in the left anterior descending coronary artery for at least 45 min. Hemodynamic monitoring and signal averaging of X, Y, and Z electrocardiographic leads were performed (150 beats, filtered at 50 Hz). After reperfusion, all animals developed an accelerated idioventricular rhythm and high creatine kinase (CPK) plasma levels. Coronary venous purines and catecholamines increased transiently. Two hours after reperfusion, heart rate was elevated from the initial 87.5 +/- 6.3 to 126 +/- 6.4 beats/min (p less than 0.01) and the pressure-rate product (PRP, an index of oxygen demand) from 9,530 +/- 630 to 11,950 +/- 790 mm Hg/min (p less than 0.05). After 2 weeks, six surviving pigs had a decreased stroke volume (98 +/- 18 versus the initial 124 +/- 14 microliters/kg, p less than 0.05), a prolonged high-frequency signal-averaged QRS duration (81.2 +/- 6.5 versus 65.7 +/- 2.9 ms, initially; p less than 0.05), and ventricular tachycardias (VTs), inducible by programmed electrical stimulation (PES). After the infusion of isradipine (1 microgram/kg/min for 30 min), the cardiac index increased from 92 +/- 14 to 133 +/- 8.7 ml/min.kg (p less than 0.02). Even at a higher heart rate, the PRP dropped from 12,600 +/- 1,900 to 10,560 +/- 1,400 mm Hg/min (p less than 0.05). Sustained monomorphic tachycardias were inducible in five pigs before and in three pigs after isradipine, and no deterioration of the signal-averaged electrocardiogram parameters was found.(ABSTRACT TRUNCATED AT 250 WORDS)
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Langen et al. (1990) studied Chronic myocardial infarction (n=6). Isradipine vs. Baseline (before isradipine infusion) was evaluated on Cardiac index and pressure-rate product (p=<0.02). In a pig model of healed myocardial infarction, isradipine infusion significantly increased cardiac index (P<0.02) and decreased the pressure-rate product (P<0.05).
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