Phase 2 ventricular arrhythmias in acute myocardial infarction: a neglected target for therapeutic antiarrhythmic drug development and for safety pharmacology evaluation
Open Access
- 1 July 2005
- journal article
- review article
- Published by Wiley in British Journal of Pharmacology
- Vol. 145 (5) , 551-564
- https://doi.org/10.1038/sj.bjp.0706231
Abstract
Ventricular fibrillation (VF), a cause of sudden cardiac death (SCD) in the setting of acute myocardial infarction (MI), remains a major therapeutic challenge. In humans, VF may occur within minutes or hours after the onset of chest pain, so its precise timing in relation to the onset of ischaemia is variable. Moreover, because VF usually occurs unobserved, out of hospital, and is usually lethal in the absence of intervention, its precise timing of onset is actually unknown in most patients. In animal models, the timing of susceptibility to VF is much better characterised. It occurs in two distinct phases. Early VF (defined as phase 1 VF, with possible subphases 1a and 1b in some animal species) occurs during the first 30 min of ischaemia when most myocardial injury is still reversible. Late VF, defined as phase 2 VF, occurs when myocardial necrosis is becoming established (after more than 90 min of ischaemia). Although much is known about the mechanisms and pharmacology of phase 1 VF, little is known about phase 2 VF. By reviewing a range of different types of data we have outlined the likely mechanisms and clinical relevance of phase 2 VF, and have evaluated possible future directions to help evolve a strategy for its suppression by drugs. The possibility that a proarrhythmic effect on phase 2 VF contributes to the adverse cardiac effects of certain cardiac and noncardiac drugs is also discussed in relation to the emerging field of safety pharmacology. It is concluded that suppression of phase 2 as well as phase 1 VF will almost certainly be necessary if drugs of the future are to achieve what drugs of the past and present have failed to achieve: full protection against SCD. Likewise, safety will require avoidance of exacerbation of phase 2 as well as phase 1 VF.British Journal of Pharmacology (2005) 145, 551–564. doi:10.1038/sj.bjp.0706231Keywords
This publication has 138 references indexed in Scilit:
- Evaluation of Drug-Induced QT Interval ProlongationDrug Safety, 2001
- Resident Cardiac Mast Cells Degranulate and Release Preformed TNF-α, Initiating the Cytokine Cascade in Experimental Canine Myocardial Ischemia/ReperfusionCirculation, 1998
- Effects of anipamil, a long acting analog of verapamil, in pigs subjected to myocardial ischemiaLife Sciences, 1995
- A modified model of global ischaemia: application to the study of syncytial mechanisms of arrhythmogenesisCardiovascular Research, 1992
- Autonomic mechanisms in ventricular fibrillation induced by myocardial ischemia during exercise in dogs with healed myocardial infarction. An experimental preparation for sudden cardiac death.Circulation, 1984
- Effect of acute coronary artery occlusion on local myocardial extracellular K+ activity in swine.Circulation, 1980
- Subendocardial origin of ventricular arrhythmias in 24-hour-old experimental myocardial infarction.Circulation, 1976
- Morphologic correlates of technetium-99m stannous pyrophosphate imaging of acute myocardial infarcts in dogs.Circulation, 1975
- Delayed Development of Ventricular Ectopic Rhythms following Experimental Coronary OcclusionCirculation, 1950
- Terminal electrocardiographic patterns in experimental anoxia, coronary occlusion, and hemorrhagic shockAmerican Heart Journal, 1948