Copyright © 1993 by the European Society of Cardiology.
© 1993 The European Society of Cardiology
Coronary haemodynamics and vasodilatory profile of a potassium channel opener in patients with coronary artery disease
Department of Cardiology, Hospital de Weezenlanden Zwolle, The Netherlands
Correspondence to: Harry Suryaprantata, MD, PhD, FESC, Department of cadiology, Hospital de Weezenlanden, Groot Wezenland 20, 8011 JW Zwolle, The Netherlands.
Previous studies have indicated that nicorandil reduces both preload and afterload, clearly distinguishing nicorandil from conventional nitrates, whose predominant action is that of preload reduction. In association with the decrease in afterload following nicorandil, the contractile responses during isovolumic contraction and relaxation improved significantly, indicating that nicorandil does not demonstrate negative inotropic actions. Furthermore, despite a marked decrease in mean aortic pressure after nicorandil, coronary sinus blood flow remains unchanged. Therefore, coronary vasodilatation must have taken place, while myocardial oxygen consumption decreased significantly. The vasodilatory action of nicorandil on the epicardial coronary artery has also been demonstrated in our previous study. Nicorandil, at a dose of either 20 or 40 mg, induces a significant increase in coronary artery diameter favourably by acting not only on the non-stenotic but also on the stenotic coronary segments.
In our recent study, the effects of intracoronary nicorandil (6µ. kg–) and isosorbide dinitrate (2 mg) on the epicardial coronary arteries were investigated in patients undergoing coronary angioplasty. In non-stenotic coronary artery segments, the mean coronary diameter increased significantly after either nicorandil (+ 12%) or isosorbide dinitrate (+ 17%). In stenotic segments, however, increase in the diameter of the obstructed segment by 20% after intracoronary nicorandil was much more pronounced when compared to that of 8% after isosorbide dinitrate. There was a significant additional increase of 13% in the diameter of the obstructed segment when nicorandil was administered following isosorbide dinitrate, while no such additional effect was observed when isosorbide dinitrate was given after nicorandil.
In summary, the potential advantage of nicorandil is that, at anti-anginal doses, it has a coronary vasodilating action combined with a balanced peripheral vasodilatation, which leads to a decrease in both preload and afterload. Therefore, nicorandil affects two of the main haemodynamic determinants of oxygen demand without impairing myocardial contractility. More importantly, both intracoronary nicorandil and isosorbide dinitrate induce significant vasodilatation in non-stenotic coronary arteries, but nicorandil appears to be more potent than isosorbide dinitrate in dilating stenotic coronary segments.
Key Words: Haemodynamics • nicorandil • vasodilatory action.
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