Why the study?
This study assessed the effects of intravenous amiodarone pretreatment on myocardial energy metabolism and mechanical function in perfused isovolumic rat hearts during ischemia and reperfusion.
Effects of amiodarone injected intravenously (i.v.) at two doses (10 and 20 mg/kg) on perfused isovolumic rat hearts were assessed by P-31 nuclear magnetic resonance (NMR). P-31 NMR is used to measure intracellular myocardial pH, phosphocreatine (PCr), and ATP contents time evolutions. Myocardial mechanical function is estimated by heart rate (HR), left ventricular developed pressure (LVP), and coronary flow (CF). In experimental procedure A (2-h retrograde perfusion), drug injection induced a dose-dependent bradycardia (10-20%) and a slight decrease in LVP but did not affect CF, pH, PCr, or ATP contents. Experimental procedure B consisted of 30-min stabilization, 18-min ischemia, and 72-min reperfusion. During ischemia, amiodarone did not preserve ATP and PCr pools and did not alleviate acidosis. ATP decreased to 30% of its control values, whereas the PCr peak was hardly detectable after 12 min of ischemia. After 24 min of reflow, HR, PCr, and pH of treated hearts recovered. LVP recovered after 36 min, whereas for control hearts, HR, PCr, and pH recovered after 42 min and LVP did not reach its control values at the end of reperfusion time. Faster pH recovery is explained by a preservation of Na+/K+ ATPase due to the influence of amiodarone on membrane lipid dynamics.
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Elst et al. (1990) studied Metastatic melanoma (B16-F10 pulmonary metastasis mouse model) / Myocardial ischemia (rat model in abstract) (n=12). Desethylamiodarone (DEA) vs. Vehicle control (100 μl 0.9% saline solution containing 10% ethanol) was evaluated on Total apoptosis rate in B16-F10 melanoma cells at 24 hours (10 μM DEA) and in vivo lung metastasis formation (p=≤0.001).
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