[Heart rate and experimental myocardial ischaemia]
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Updated: Aug 20, 2026

Semi-Minimal Invasive Method to Induce Myocardial Infarction in Rats and the Assessment of Cardiac Function by an Isolated Working Heart System
Published on: June 11, 2020
Alain Berdeaux1, Patrice Colin, Xavier Monnet
1Laboratoire de Pharmacologie, Inserm, Faculté de Médecine, Créteil, France. berdeaux@im3.inserm.fr
Insights
Reducing heart rate is crucial in cardiology. If current inhibitors, unlike beta-blockers, offer cardiac benefits by lowering heart rate without negatively impacting contractility, improving outcomes in ischemia-reperfusion injury.
Area of Science:
- Cardiology
- Pharmacology
Context:
- Elevated heart rate is a poor prognostic indicator in cardiovascular disease.
- Reducing heart rate is a significant therapeutic goal.
Purpose:
- To compare the effects of If current inhibitors and beta-blockers on myocardial oxygen consumption and diastolic perfusion.
- To evaluate the therapeutic benefits of heart rate reduction strategies.
Summary:
- Both If current inhibitors and beta-blockers reduce myocardial oxygen consumption by lowering heart rate.
- Unlike beta-blockers, If current inhibitors do not significantly decrease myocardial contractility.
- This lack of negative inotropic effect in If current inhibitors leads to longer diastolic perfusion times, which is advantageous during ischemia-reperfusion.
Impact:
- If current inhibitors demonstrate superior benefits over beta-blockers in managing myocardial dysfunction associated with cardiac ischemia-reperfusion.
- These findings highlight the potential of If current inhibitors in treating conditions like myocardial stunning.
Abstract:
Every increase in heart rate represents a poor prognostic factor in cardiology, and multiple arguments have now led to the belief that reducing heart rate is a major therapeutic challenge. A comparison of the pharmacological effects of If current inhibitors such as zatebradine, and more recently ivabradine (Procoralan) and beta-blockers, have demonstrated experimentally that reductions in heart rate and myocardial contractile force contribute equally to the reduction in myocardial oxygen consumption in the normal heart. Conversely, at a similar level of reduction in heart rate, the lack of a concomitant negative inotropic effect with ivabradine affords longer diastolic perfusion times than beta-blockers. In other words, a negative inotropic effect is deleterious when an increase in coronary blood flow is required. Hence, if the anti-ischaemic effects afforded by an If current inhibitor and a beta-blocker are roughly comparable, the former are clearly of higher benefit than beta-blockers in the treatment of myocardial dysfunction accompanying cardiac ischaemia-reperfusion, especially myocardial stunning.
