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Updated: Jun 11, 2025

Voltage-Dependent Potassium Current Recording on H9c2 Cardiomyocytes via the Whole-Cell Patch-Clamp Technique
Published on: November 11, 2022
Inhibition of hERG K channels by verapamil at physiological temperature: Implications for the CiPA initiative
Ashley A Johnson1, Matthew C Trudeau1
1Department of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201, United States of America.
Insights
A revised electrophysiology protocol significantly improves the success rate for measuring drug inhibition of hERG channels, crucial for assessing cardiac arrhythmia risk. This optimized method enhances the practicality of data generation for the Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative.
Area of Science:
- Cardiovascular Pharmacology
- Electrophysiology
- Drug Safety Assessment
Background:
- The Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative shifts focus from solely hERG channel inhibition to a broader assessment of drug-induced Torsades de Pointes (TdP).
- Accurate determination of hERG channel inhibitory properties is essential for predicting drug-induced cardiac arrhythmias.
Purpose of the Study:
- To evaluate a revised data acquisition protocol for measuring hERG channel inhibition at physiological temperature (37°C) within the CiPA framework.
- To compare the efficacy and practicality of a revised protocol against the standard CiPA protocol for determining verapamil's hERG inhibitory properties.
Main Methods:
- Manual whole-cell patch-clamp electrophysiology was used to record hERG1a potassium channel inhibition by verapamil.
- The standard CiPA protocol involved 10s voltage steps to 0mV, with a cumulative recording time of ~30 min.
- A revised protocol utilized shorter 3s voltage steps to 0mV, reducing cumulative recording time to ~10 min.
Main Results:
- The standard protocol yielded an IC50 of 225 nM for verapamil but had a low experimental success rate (5%).
- The revised protocol produced similar IC50 (252 nM) and Hill coefficient (0.8) values, indicating comparable pharmacological data.
- The revised protocol increased the experimental success rate five-fold to 25%, enhancing feasibility for biophysical studies.
Conclusions:
- The revised electrophysiology protocol demonstrates increased practicality and feasibility for generating hERG channel drug inhibition data.
- This optimized protocol provides reliable pharmacological data comparable to the standard protocol with significantly improved success rates.
- The revised protocol is proposed as a more pragmatic approach for hERG channel drug inhibition assessments in CiPA and regulatory science.
Abstract:
The Comprehensive in vitro Proarrhythmia Assay (CiPA) initiative reassesses using the inhibition of hERG potassium channels by drugs as the major determinant for the potential to cause drug-induced Torsades de Pointes (TdP) cardiac arrhythmias. Here we report our findings on the next phase of CiPA: Determination of hERG inhibitory properties using the standard CiPA-defined data acquisition protocol, here called the standard protocol, at physiological temperature (37 degrees Celsius). To do this, we measured inhibition of hERG1a potassium channels stably expressed in HEK293 cells by the small molecule verapamil, using manual whole-cell patch-clamp electrophysiology recordings with the standard protocol, which is characterized, in part, by a series of 10 s duration voltage steps to 0 mV, ultimately leading to a cumulative recording time of approximately 30 min. Using the standard protocol, we measured an IC50 for verapamil of 225 nM, a Hill coefficient of 1, and time constant of inhibition at 0 mV of 0.64 s. But, using the standard protocol resulted in a very low (5 %) experimental success rate per cell, which had low practicality for future experiments. To address the 5 % success rate, we generated a revised protocol characterized, in part, by a series of 3 s duration voltage steps to 0 mV, leading to a cumulative recording time of approximately 10 min. Using the revised protocol, we found an IC50 for verapamil of 252 nM, a Hill coefficient of 0.8, and time constant of inhibition at 0 mV of 0.67 s. The values measured with the revised protocol were similar to those measured using the standard protocol and, furthermore, our success rate using the revised protocol rose to 25 %, an increase of 5-fold over the standard protocol, and more in line with the success rate for biophysical studies. In summary, we captured key pharmacological data for subsequent analysis in CiPA using a revised protocol with an increased success rate and an overall enhanced feasibility and practicality. We propose that the revised protocol may be more pragmatic for generation of some hERG channel drug inhibition data for CiPA and other regulatory sciences.
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