Referenced in: none

Automatically associated channels: Kir2.1 , Kv11.1 , Kv7.1 , Nav1.5

Title: Cellular mechanism of the QT prolongation induced by sulpiride.

Authors: Hyang-Ae Lee, Ki-Suk Kim, Sang-Joon Park, Eun-Joo Kim

Journal, date & volume: Int. J. Toxicol., 2009 May-Jun , 28, 207-12

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19546258

Abstract
In this study, the authors investigated the electrophysiological effect of sulpiride on cardiac repolarization using conventional microelectrode recording techniques in isolated canine Purkinje fibers and a whole-cell patch clamp technique in transiently transfected cells with the hERG, KCNQ1/KCNE1, KCNJ2, and SCN5A cDNA and in rat cardiac myocytes for I(Ca). In studies of action potential duration, 10 microM, 100 microM, 300 microM, and 1 mM sulpiride prolonged action potential duration in a concentration-dependent manner. In studies of cardiac ion channels, sulpiride did not significantly affect I(Na), I(Ca), I(Ks), I(K1), except for I(Kr). Sulpiride dose-dependently decreased the hERG tail current. It is considered that the prolonged action potential duration by sulpiride was mainly the result of inhibition of the hERG channel. The data suggest that the clinical use of sulpiride is reasonable within therapeutic plasma concentrations, but all patients taking this drug should be cautiously monitored for clinical signs of long-QT syndrome and severe arrhythmia.