Clinical Pharmacology & Therapeutics · 2015 · 146 citations · 33 references
MedicineCardiologyPharmacologyCardiovascular PharmacotherapyClinical PharmacologyElectrophysiologyAntiarrhythmic TherapyArrhythmia PharmacotherapyCardiac Ion ChannelsCardiac MedicationsCardiac PharmacotherapyIon Channel PharmacologyDiltiazem TherapyDofetilide TherapyLate Sodium CurrentLong Qt Syndrome ScreeningMexiletine TherapyPotassium Channel BlockadePotassium Channel BlockersPotassium Channel Pharmacology
Drug-induced long QT syndrome has resulted in many drugs being withdrawn from the market. At the same time, the current regulatory paradigm for screening new drugs causing long QT syndrome is preventing drugs from reaching the market, sometimes inappropriately. In this study, we report the results of a first-of-a-kind clinical trial studying late sodium (mexiletine and lidocaine) and calcium (diltiazem) current blocking drugs to counteract the effects of hERG potassium channel blocking drugs (dofetilide and moxifloxacin). We demonstrate that both mexiletine and lidocaine substantially reduce heart-rate corrected QT (QTc) prolongation from dofetilide by 20 ms. Furthermore, all QTc shortening occurs in the heart-rate corrected J-Tpeak (J-Tpeak c) interval, the biomarker we identified as a sign of late sodium current block. This clinical trial demonstrates that late sodium blocking drugs can substantially reduce QTc prolongation from hERG potassium channel block and assessment of J-Tpeak c may add value beyond only assessing QTc.
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HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
Matthew C. Trudeau, Jeffrey W. Warmke, Barry Ganetzky et al. · Science · 1995 · 1.2K citations
Peter J. Schwartz, Silvia G. Priori, Emanuela H. Locati et al. · Circulation · 1995 · 816 citations
Medicine, Cardiology, Pharmacology +16