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• W2147702220 endingPage "437" @default.
• W2147702220 startingPage "429" @default.
• W2147702220 abstract "Promethazine is a phenothiazine derivative with antihistaminic (H1), sedative, antiemetic, anticholinergic, and antimotion sickness properties that can induce QT prolongation, which may lead to torsades de pointes. Since block of cardiac human ether-a-go-go-related gene (hERG) channels is one of the leading causes of acquired long QT syndrome, we investigated the acute effects of promethazine on hERG channels to determine the electrophysiological basis for its proarrhythmic potential. Promethazine increased the action potential duration at 90% of repolarization (APD90) in a concentration-dependent manner, with an IC50 of 0.73 μM when action potentials were elicited under current clamp in guinea pig ventricular myocytes. We examined the effects of promethazine on the hERG channels expressed in Xenopus oocytes and HEK293 cells using two-microelectrode voltage-clamp and patch-clamp techniques. Promethazine induced a concentration-dependent decrease of the current amplitude at the end of the voltage steps and hERG tail currents. The IC50 of promethazine dependent hERG block in Xenopus oocytes decreased progressively relative to the degree of depolarization. The IC50 for the promethazine-induced block of the hERG currents in HEK293 cells at 36 °C was 1.46 μM at +20 mV. Promethazine affected the channels in the activated and inactivated states but not in the closed states. The S6 domain mutations, Y652A and F656A partially attenuated (Y652A) or abolished (F656A) the hERG current block. These results suggest that promethazine is a blocker of the hERG channels, providing a molecular mechanism for the arrhythmogenic side effects during the clinical administration of promethazine." @default.
• W2147702220 created "2016-06-24" @default.
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• W2147702220 date "2009-11-01" @default.
• W2147702220 modified "2023-10-02" @default.
• W2147702220 title "H1 antihistamine drug promethazine directly blocks hERG K+ channel" @default.
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• W2147702220 doi "https://doi.org/10.1016/j.phrs.2009.05.008" @default.
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