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Br J Pharmacol. 2007 Aug;151(8):1368-76. Epub 2007 Jun 25.

State dependent dissociation of HERG channel inhibitors.

Author information

1
Department of Pharmacology and Toxicology, University of Vienna, Althanstrasse 14, Vienna 1090, Austria.

Abstract

BACKGROUND AND PURPOSE:

Inhibition of HERG channels prolongs the ventricular action potential and the QT interval with the risk of torsade de pointes arrhythmias and sudden cardiac death. Many drugs induce greater inhibition of HERG channels when the cell membrane is depolarized frequently. The dependence of inhibition on the pulsing rate may yield different IC(50) values at different frequencies and thus affect the quantification of HERG channel block. We systematically compared the kinetics of HERG channel inhibition and recovery from block by 8 blockers at different frequencies.

EXPERIMENTAL APPROACH:

HERG channels were expressed heterologously in Xenopus oocytes and currents were measured with the two-electrode voltage clamp technique.

KEY RESULTS:

Frequency-dependent block was observed for amiodarone, cisapride, droperidol and haloperidol (group 1) whereas bepridil, domperidone, E-4031 and terfenadine (group 2) induced similar pulse-dependent block at all frequencies. With the group 1 compounds, HERG channels recovered from block in the presence of drug (recovery being voltage-dependent). No substantial recovery from block was observed with the second group of compounds. Washing out of bepridil, domperidone, E-4031 and terfenadine was substantially augmented by frequent pulsing. Mutation D540K in the HERG channel (which exhibits reopening at negative voltages) facilitated recovery from block by these compounds at -140 mV.

CONCLUSION AND IMPLICATIONS:

Drug molecules dissociate at different rates from open and closed HERG channels ('use-dependent' dissociation). Our data suggest that apparently 'trapped' drugs (group 2) dissociated from the open channel state whereas group 1 compounds dissociated from open and resting states.

PMID:
17592502
PMCID:
PMC2189824
DOI:
10.1038/sj.bjp.0707356
[Indexed for MEDLINE]
Free PMC Article

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