# Dominant ionic currents in rabbit ventricular action potential dynamics

**Authors:** Zhechao Yang, Hao Gao, Godfrey L. Smith, Radostin D. Simitev, Pan Li, Pan Li, Pan Li, Pan Li

PMC · DOI: 10.1371/journal.pone.0328261 · PLOS One · 2025-07-30

## TL;DR

This study identifies key ion currents that most influence the electrical activity of rabbit heart cells, improving the model's usefulness for personalized simulations.

## Contribution

The study introduces a method to simplify cardiac models by identifying dominant ion currents using sensitivity analysis.

## Key findings

- The background chloride current is the main factor influencing action potential variability.
- Six key ion currents significantly affect action potential biomarkers like duration and resting potential.
- A simplified model with six parameters captures individual biomarkers with high accuracy.

## Abstract

Mathematical models of cardiac cell electrical activity include numerous parameters, making calibration to experimental data and individual-specific modeling challenging. This study applies Sobol sensitivity analysis, a global variance-decomposition method, to identify the most influential parameters in the Shannon model of rabbit ventricular myocyte action potential (AP). The analysis highlights the background chloride current (IClb) as the dominant determinant of AP variability. Additionally, the inward rectifier potassium current (IK1), fast/slow delayed rectifier potassium currents (IKr, IKs), sodium-calcium exchanger current (INaCa), the slow component of the transient outward potassium current (Itos), and L-type calcium current (ICaL) significantly affect AP biomarkers, including duration, plateau potential, and resting potential. Exploiting these results, a hierarchical reduction of the model is performed and demonstrates that retaining only six key parameters can capture sufficiently well individual biomarkers, with a coefficient of determination exceeding 0.9 for selected cases. These findings improve the utility of the Shannon model for personalized simulations, aiding applications like digital twins and drug response predictions in biomedical research.

In our study, we explored the complexity of a mathematical model used to understand the electrical activity of rabbit ventricular cells. Such models involve many parameters, which makes it difficult to match them with experimental data or to personalize them for individual cells. To address this, we used a method for global sensitivity analysis to identify which ion current parameters have the most impact on the action potential output of the model. Our analysis shows that the background chloride current is the main factor influencing the variability of the rabbit ventricular action potential. Other important currents include the inward rectifier potassium current, various potassium currents, sodium-calcium exchanger current, the slow component of the transient outward potassium current, and the L-type calcium current. These factors play a significant role in determining key features of the action potential, such as its duration, plateau potential, and resting potential. Based on these results, we proposed a sequence of simplified models obtained by retaining variability in a few most influential parameters while fixing the rest to appropriate constant values. This approach is also applicable to other mathematical models of cardiac action potentials and can make them more useful for personalized simulations, and in areas like digital twins and predicting drug responses in biomedical research.

## Full-text entities

- **Genes:** KCNH2 (potassium voltage-gated channel subfamily H member 2) [NCBI Gene 3757] {aka ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1}, SLC24A3 (solute carrier family 24 member 3) [NCBI Gene 57419] {aka NCKX3}, KCNN4 (potassium calcium-activated channel subfamily N member 4) [NCBI Gene 3783] {aka DHS2, IK, IK1, IKCA1, KCA4, KCa3.1}, SLC8A1 (solute carrier family 8 member A1) [NCBI Gene 6546] {aka NCX1}, TLX2 (T cell leukemia homeobox 2) [NCBI Gene 3196] {aka HOX11L1, NCX}
- **Diseases:** AP (MESH:D009207), long QT (MESH:D008133), arrhythmic (OMIM:212500), POINTS (MESH:C000719195), fibrillation (MESH:D014693)
- **Chemicals:** Cl (MESH:D002713), chloride (MESH:D002712), K + (MESH:D011188), Ca (MESH:D002118), Ca2 + (-), Na+ (MESH:D012964)
- **Species:** Homo sapiens (human, species) [taxon 9606], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12310051/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12310051/full.md

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Source: https://tomesphere.com/paper/PMC12310051