Circulation, Vol 76, 916-928, Copyright © 1987 by American Heart Association
GM Pieper and GJ Gross
The effects of two antianginal drugs, nicorandil and isosorbide dinitrate
(ISDN), on metabolism and function of the ischemic myocardium were studied
in a preparation of multiple coronary occlusions in barbital-anesthetized
dogs. The preparation consisted of three 5 min occlusions of the left
anterior descending coronary artery interspersed by 30 min of reperfusion.
An equihypotensive dose of nicorandil (7.5 micrograms/kg/min) or ISDN (12.5
micrograms/kg/min) was infused 15 min before and during the second
occlusion period. Hemodynamics, myocardial segment shortening (%SS), tissue
blood flow, and myocardial oxygen consumption were determined throughout.
Uptake of free fatty acids (FFA), glucose, and lactate were determined
during control and ischemic periods. At the end of the final 30 min
reperfusion period, biopsy samples of transmural tissue were taken for
analysis of phosphocreatine, adenine nucleotides, and total tissue water
content. No major hemodynamic changes were produced by either drug except
for a 5 to 10 mm Hg decrease in mean aortic pressure. Compared with
untreated and ISDN-treated hearts, hearts of dogs treated with nicorandil
exhibited reversal of a significant increase in FFA uptake during recurrent
ischemia. This was accompanied by an attenuation of the increase in oxygen
extraction and CO2 production in the ischemic zone by nicorandil, but not
by ISDN. Nicorandil, but not ISDN, improved %SS during reperfusion.
Endocardial ATP and total adenine nucleotides were preserved in both
nicorandil- and ISDN-treated hearts. Tissue edema was also attenuated by
both compounds. Thus, nicorandil improved both function and metabolism
during recurrent myocardial ischemia independent of a hemodynamic effect,
whereas ISDN only attenuated the loss of adenine nucleotides and increase
in tissue water.
ARTICLES
Salutary action of nicorandil, a new antianginal drug, on myocardial metabolism during ischemia and on postischemic function in a canine preparation of brief, repetitive coronary artery occlusions: comparison with isosorbide dinitrate
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee 53226.
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