Related Experiment Video
Updated: Aug 9, 2026

Measurement of Antibody Effects on Cellular Function of Isolated Cardiomyocytes
Published on: March 8, 2013
Anti-ischaemic effect of ivabradine
Roberto Ferrari1, Anna Cargnoni, Claudio Ceconi
1University of Ferrara, Italy. fri@dns.unife.it
Insights
Ivabradine selectively inhibits the If current to reduce heart rate without negative inotropic effects. This heart rate reduction improves myocardial energetics and perfusion in patients with chronic ischemic heart disease.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Ivabradine is a novel heart rate-reducing agent.
- It selectively inhibits the If current in the sinoatrial node.
Purpose of the Study:
- To investigate the effects of ivabradine on heart rate and myocardial function.
- To explore the clinical benefits of ivabradine in patients with chronic ischemic heart disease.
Main Methods:
- Selective inhibition of the If current.
- Electrophysiological studies to assess diastolic depolarization.
- Evaluation of myocardial perfusion and contractility during exercise and ischemia.
- Assessment of left ventricular function in heart failure and post-myocardial infarction.
Main Results:
- Ivabradine reduces heart rate by decreasing the slope of diastolic depolarization.
- It preserves coronary vasodilatation and myocardial perfusion during exercise.
- No negative inotropic effects or reduction in cardiac contractility were observed.
- Ivabradine demonstrated protective effects during myocardial ischemia, improved left ventricular function in heart failure, and reduced remodeling post-myocardial infarction.
Conclusions:
- Selective If current inhibition with ivabradine offers a pure heart rate reduction.
- This mechanism decreases myocardial oxygen demand, improves energetics, and enhances perfusion in ischemic myocardium.
- Distinct clinical benefits are anticipated from long-term heart rate reduction using ivabradine in chronic ischemic heart disease patients.
Abstract:
Ivabradine, the first representative of a new class of exclusive heart rate-reducing agents, selectively inhibits the I(f) current in the sinoatrial node. The direct electrophysiological consequence of this inhibition is a reduction in the slope of the diastolic depolarisation curve and a decrease in heart rate. Pharmacological inhibition of the I(f) current with ivabradine has been shown to preserve coronary vasodilatation upon exercise, i.e., myocardial perfusion, with no negative inotropic effects and maintenance of cardiac contractility. Ivabradine protects the myocardium during ischaemia, improves left ventricular function in congestive heart failure, and reduces remodelling subsequent to myocardial infarction. Pure heart rate reduction by specific and selective I(f) inhibition decreases oxygen demand, improves myocardial energetics and improves perfusion of the ischaemic myocardium. We can expect distinct clinical benefits from long-term heart rate reduction in patients with chronic ischaemic disease.
Related Concept Videos
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antianginal Drugs: Calcium Channel Blockers and Ranolazine
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

