Electrophysiological and Pharmacological Characterization of Human Inwardly Rectifying K ir 2.1 Channels on an Automated Patch-Clamp Platform

• Published in: Assay and drug development technologies Vol. 17; no. 3; p. 89
• Main Authors: Sanson, Camille, Schombert, Brigitte, Filoche-Rommé, Bruno, Partiseti, Michel, Bohme, G Andrees
• Format: Journal Article
• Language: English
• Published: United States 01-04-2019
• Subjects: Animals; Automation; Chloroquine - chemistry; Chloroquine - pharmacology; CHO Cells; Cricetulus; Dose-Response Relationship, Drug; Electrophysiological Phenomena; Humans; Imidazoles - chemistry; Imidazoles - pharmacology; Molecular Structure; Pentamidine - analogs & derivatives; Pentamidine - chemistry; Pentamidine - pharmacology; Phenanthrolines - chemistry; Phenanthrolines - pharmacology; Potassium Channels, Inwardly Rectifying - antagonists & inhibitors; Potassium Channels, Inwardly Rectifying - metabolism; ventricular arrhythmia; sudden death; CiPA initiative; torsades de pointes; safety pharmacology; K channels
• ISSN: 1557-8127
• DOI: 10.1089/adt.2018.882

Inwardly rectifying I
potassium currents of the heart control the resting membrane potential of ventricular cardiomyocytes during diastole and contribute to their repolarization after each action potential. Mutations in the gene encoding K
2.1 channels, which primarily conduct ventricular I
, are associated with inheritable forms of arrhythmias and sudden cardiac death. Therefore, potential iatrogenic inhibition of K
2.1-mediated I
currents is a cardiosafety concern during new drug discovery and development. K
2.1 channels are part of the panel of cardiac ion channels currently considered for refined early compound risk assessment within the Comprehensive in vitro Proarrhythmia Assay initiative. In this study, we have validated a cell-based assay allowing functional quantification of K
2.1 inhibitors using whole-cell recordings of Chinese hamster ovary cells stably expressing human K
2.1 channels. We reproduced key electrophysiological and pharmacological features known for native I
, including current enhancement by external potassium and voltage- and concentration-dependent blockade by external barium. Furthermore, the K
inhibitors ML133, PA-6, and chloroquine, as well as the multichannel inhibitors chloroethylclonidine, chlorpromazine, SKF-96365, and the class III antiarrhythmic agent terikalant demonstrated slowly developing inhibitory activity in the low micromolar range. The robustness of this assay authorizes medium throughput screening for cardiosafety purposes and could help to enrich the currently limited K
2.1 pharmacology.