Referenced in: none

Automatically associated channels: Kv11.1

Title: Drugs and trafficking of ion channels: a new pro-arrhythmic threat on the horizon?

Authors: M A G van der Heyden, M E Smits, M A Vos

Journal, date & volume: Br. J. Pharmacol., 2008 Feb , 153, 406-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18059314

Abstract
Tuning of functional expression levels of the ion channels that make up the cardiac action potential (AP) is crucial for preserving correct AP duration (APD) and QTc times. Many compounds inhibit human ether-à-go-go related gene (hERG)-mediated delayed rectifier currents and thus prolong cardiac repolarization that may cause life-threatening arrhythmias like Torsades de Pointes. An increasing number of drugs are found to inhibit hERG function by a dual mechanism of short-term channel block and long-term trafficking defects that operate over different time and concentration scales. In safety screens at present used by pharmaceutical companies, the short-term effect of channel block is covered. In contrast, specific screening for long-term trafficking defects is not common, with the consequent risk of drugs that disturb trafficking entering the market. Whether that poses another pro-arrhythmic threat for the patients treated has to be determined, but is not unlikely.