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Effects of common antitussive drugs on the hERG potassium channel current.
- Source :
-
Journal of cardiovascular pharmacology [J Cardiovasc Pharmacol] 2008 Dec; Vol. 52 (6), pp. 494-9. - Publication Year :
- 2008
-
Abstract
- A common over-the-counter (OTC) non-opioid antitussive drug, clobutinol, was recently withdrawn from the market due to its potential to induce cardiac arrhythmias by a blockade of the potassium channel coded by the human ether-à-go-go-related gene (hERG). In this study, we investigated the effects of a number of antitussive compounds on the hERG ion channel current using patch-clamp electrophysiology, and compared the effects to that of clobutinol. The compounds clobutinol, pentoxyverine, dextromethorphan, and codeine inhibited the outward current in hERG transfected cells with half-maximal inhibition concentrations (IC50) of 1.9 microM, 3.0 microM, 5.1 microM, and 97 microM, respectively. For theobromine, no significant effect on the hERG current at a concentration up to 100 microM was detected. Safety margins between the effects of the drugs on the hERG ion channel current and their calculated maximal free therapeutic plasma concentration were calculated. These results were compared to assess potential risks of the compounds to induce torsade de pointes-type arrhythmias.
- Subjects :
- Amino Alcohols toxicity
Animals
CHO Cells
Codeine toxicity
Cricetinae
Cricetulus
Cyclopentanes toxicity
Dextromethorphan toxicity
Dose-Response Relationship, Drug
ERG1 Potassium Channel
Ether-A-Go-Go Potassium Channels genetics
Ether-A-Go-Go Potassium Channels metabolism
Humans
Membrane Potentials
Theobromine toxicity
Time Factors
Torsades de Pointes metabolism
Transfection
Antitussive Agents toxicity
Ether-A-Go-Go Potassium Channels antagonists & inhibitors
Potassium metabolism
Potassium Channel Blockers adverse effects
Torsades de Pointes chemically induced
Subjects
Details
- Language :
- English
- ISSN :
- 1533-4023
- Volume :
- 52
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of cardiovascular pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 19034038
- Full Text :
- https://doi.org/10.1097/FJC.0b013e31818eec8d