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Updated: Feb 24, 2026

Voltage-Dependent Potassium Current Recording on H9c2 Cardiomyocytes via the Whole-Cell Patch-Clamp Technique
Published on: November 11, 2022
Effects of equol on multiple K+ channels stably expressed in HEK 293 cells
Xiu-Ling Deng1, Yan Wang2, Guo-Sheng Xiao2
1Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, China.
Insights
Equol affects cardiovascular potassium (K+) channels, inhibiting some while increasing others at specific concentrations. This suggests equol
Area of Science:
- Cardiovascular pharmacology
- Molecular biology
- Electrophysiology
Background:
- Potassium channels play critical roles in cardiovascular function.
- Equol's effects on cardiac ion channels are not fully understood.
- Investigating equol's impact on cardiovascular K+ channels is crucial for understanding its therapeutic potential.
Purpose of the Study:
- To investigate the effects of equol on various cardiovascular potassium (K+) channel currents.
- To determine the concentration-dependent effects of equol on specific K+ channel subtypes.
- To evaluate equol's potential as a therapeutic agent for cardiovascular disorders.
Main Methods:
- HEK 293 cells stably expressing cloned cardiovascular K+ channels were used.
- The conventional whole-cell patch voltage-clamp technique was employed.
- Concentration-response relationships were established for equol's effects.
Main Results:
- Equol inhibited hKv1.5, hKv4.3, IKs, and IhERG currents in a concentration-dependent manner.
- Equol increased large-conductance calcium-activated potassium (BKCa) channel current at very low concentrations (EC50: 0.1 μM).
- Equol did not significantly affect guinea pig ventricular action potentials at concentrations up to 3 μM.
Conclusions:
- Equol exhibits differential effects on cardiac K+ channels, inhibiting some at higher concentrations and activating BKCa channels at lower concentrations.
- These findings suggest equol may be a safe drug candidate for cerebral vascular disorders.
- Further research is warranted to explore equol's therapeutic applications in cardiovascular conditions.
Abstract:
The present study investigated the effects of equol on cardiovascular K+ channel currents. The cardiovascular K+ channel currents were determined in HEK 293 cells stably expressing cloned differential cardiovascular K+ channels with conventional whole-cell patch voltage-clamp technique. We found that equol inhibited hKv1.5 (IC50: 15.3 μM), hKv4.3 (IC50: 29.2 μM and 11.9 μM for hKv4.3 peak current and charge area, respectively), IKs (IC50: 24.7 μM) and IhERG (IC50: 31.6 and 56.5 μM for IhERG.tail and IhERG.step, respectively), but not hKir2.1 current, in a concentration-dependent manner. Interestingly, equol increased BKCa current with an EC50 of 0.1 μM. It had no significant effect on guinea pig ventricular action potentials at concentrations of ≤3 μM. These results demonstrate that equol inhibits several cardiac K+ currents at relatively high concentrations, whereas it increases BKCa current at very low concentrations, suggesting that equol is a safe drug candidate for treating patients with cerebral vascular disorders.
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