Key result
Nisoldipine pretreatment completely prevents myocardial lipid peroxidation during coronary occlusion in pigs.
Why the study?
The effect of the Ca++ channel blocker nisoldipine on the content of lipid peroxidation products in pig myocardium after acute coronary occlusion required investigation.
Does nisoldipine prevent lipid peroxidation in pig myocardium after acute coronary occlusion?
Does nisoldipine prevent lipid peroxidation in pig myocardium after acute coronary occlusion?
Nisoldipine prevents excessive lipid peroxidation in both ischemic and non-ischemic myocardium during acute coronary occlusion in a porcine model.
Answers are grounded in this paper and cite their sources.
Nisoldipine may limit oxidative stress in porcine acute ischemia; leaves open translation to human cardioprotection.
Study objective The aim was to investigate the effect of the Ca++ channel blocker nisoldipine on the content of lipid peroxidation products in pig myocardium after acute coronary occlusion. Design Open chest pigs were subjected to the occlusion of the left anterior coronary artery (LAD) with or without nisoldipine. After 30 min ischaemia, myocardial samples were taken from the ischaemic area and from the non-ischaemic posterior wall of the left ventricle for determination of lipid peroxidation products. Subjects Subjects were farm pigs of either sex. In 10 pigs, the LAD was occluded without drug pretreatment; 11 pigs were infused with nisoldipine (10 micrograms.kg-1) 30 min before the LAD occlusion. Sham operated controls received no drug (n = 7) or nisoldipine (n = 9). Measurements and main results Myocardial samples were assayed for the content of lipid peroxidation products: malondialdehyde, conjugated double bonds, and fluorescent end products. Plasma nisoldipine concentration was measured in some experiments. Following the LAD occlusion, the content of lipid peroxidation products increased in both ischaemic and non-ischaemic myocardial regions as compared to the hearts of sham operated pigs. Pretreatment with nisoldipine completely prevented these increases. At a time of the coronary occlusion, plasma nisoldipine concentrations were within the therapeutic range. Conclusion Ca++ antagonist prevents the excessive peroxidation of myocardial membrane lipids which affects the whole myocardium when there is acute local ischaemia. Prevention of myocardial damage in the non-ischaemic region may determine survival of the infarcted heart.
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Herbaczyńska-Cedro et al. (1990) studied Acute coronary occlusion (myocardial ischaemia) (n=37). Nisoldipine vs. Untreated LAD occlusion and sham-operated controls was evaluated on Myocardial content of lipid peroxidation products (malondialdehyde, conjugated double bonds, and fluorescent end products). Nisoldipine (10 mcg/kg) given 30 min prior to 30-min coronary occlusion in pigs (n=37) completely prevented increases in myocardial lipid peroxidation products vs untreated controls.
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