Why the study?
Do verapamil, diltiazem, and nifedipine have differing effects on hemodynamics and left ventricular function during acute myocardial ischemia in dogs?
Do verapamil, diltiazem, and nifedipine have differing effects on hemodynamics and left ventricular function during acute myocardial ischemia in dogs?
The calcium channel blockers verapamil, diltiazem, and nifedipine exhibit significantly different effects on left ventricular systolic and diastolic function during myocardial ischemia relative to their vasodilator potencies.
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Verapamil and nifedipine exert opposing effects on ischemic ejection fraction in dogs; leaves open translation to human acute ischemia management.
The calcium channel-blocking drugs verapamil, diltiazem, and nifedipine are being used with increasing frequency in patients with angina pectoris due to coronary artery disease. Although each of these agents possesses negative inotropic potential, their relative effects on myocardial function in relation to their vasodilator potencies are unknown. We understood to study this in 20 conscious dogs that had partial occlusions of their circumflex coronary arteries during therapy with placebo, verapamil, nifedipine, or diltiazem. Myocardial blood flow was measured by use of microspheres, and left ventricular function was measured by radionuclide angiography. Drug effects were compared at doses causing equal decreases in mean arterial pressure and coronary vascular resistance of nonischemic myocardium. Global ejection fraction and ejection fraction of the ischemic region were significantly decreased by verapamil (p less than .01) and increased by nifedipine (p less than .001); diltiazem caused no significant changes. Verapamil significantly increased peak diastolic filling rate (p less than .001); nifedipine also increased diastolic filling rate, but only at doses that markedly decreased mean arterial pressure and coronary vascular resistance. The effect of diltiazem on diastolic filling rate was not significantly different than placebo. For doses causing an equal decrease in mean arterial pressure, verapamil decreased heart rate (p less than .001), and diltiazem and nifedipine increased heart rate (p less than .001). We conclude that the relative potencies of these three calcium channel blocking agents on left ventricular systolic and diastolic function during myocardial ischemia are different when compared with their relative vasodilator potencies. These differences may have important clinical implications.
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Urquhart et al. (1984) studied this question.
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