European Heart Journal Advance Access originally published online on February 15, 2005
European Heart Journal 2005 26(6):536-537; doi:10.1093/eurheartj/ehi155
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© The European Society of Cardiology 2005. All rights reserved. For Permissions, please e-mail: journals.permissions@oupjournals.org
The degree of potassium channel blockade and the risk of torsade de pointes: the truth, nothing but the truth, but not the whole truth
Department of Cardiology, Tel-Aviv Sourasky Medical Center and Sackler School of Medicine, Tel Aviv University, Weizman 6, Tel Aviv 64239, Israel
* Corresponding author. Tel: +972 524266859; fax: +972 36974416. E-mail address: saviskin@tasmc.health.gov.il
This editorial refers to Anti-HERG activity and the risk of drug-induced arrhythmias and sudden death
by M.L. De Bruin et al., on page 590
| The first 10% of the full text of this article appears below. |
Several anti-arrhythmic drugs, as well as medications not intended for cardiac indications, block a specific potassium channel named IKr (the rapid delayed rectifying potassium current). In the case of the anti-arrhythmic drugs, IKr channels are purposely targeted. By blocking potassium outflow currents, the anti-arrhythmic drugs prolong the action potential. This action (depicted in the electrocardiogram as prolongation of the QT interval) can be advantageous given that prolongation of the action potential also lengthens the refractory period, thereby suppressing common arrhythmias. Unfortunately, by a mechanism explained elsewhere,1 IKr blockade may lead to excessive QT prolongation and trigger a polymorphic ventricular tachyarrhythmia (torsade de pointes) that may degenerate into ventricular fibrillation. Furthermore, because of its unique three-dimensional characteristics,2 IKr channels are very easily blocked by the small molecules of numerous non-cardiac drugs. The
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Related articles in EHJ:
- Anti-HERG activity and the risk of drug-induced arrhythmias and sudden death
- M.L. De Bruin, M. Pettersson, R.H.B. Meyboom, A.W. Hoes, and H.G.M. Leufkens
EHJ 2005 26: 590-597.[Abstract] [FREE Full Text]
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