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Updated: May 2, 2026

Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
Are SR Ca content fluctuations or SR refractoriness the key to atrial cardiac alternans?: insights from a human
Carlos A Lugo1, Inma R Cantalapiedra2, Angelina Peñaranda2
1Departament de Física Aplicada, Universitat Politècnica de Catalunya. BarcelonaTech, Barcelona, Spain; Centro de Astrobiología, Instituto Nacional de Técnica Aeroespacial, Ctra de Torrejón a Ajalvir, Madrid, Spain; and.
Insights
Electromechanical alternans, a cause of cardiac arrhythmias, may stem from ryanodine receptor (RyR2) dysfunction. This study shows RyR2 refractoriness, not just sarcoplasmic reticulum calcium loading, drives cytosolic calcium alternans.
Area of Science:
- Cardiology
- Biophysics
- Computational Biology
Background:
- Electromechanical alternans contribute to cardiac arrhythmias, but their molecular basis remains unclear.
- Calcium alternans are often linked to sarcoplasmic reticulum (SR) calcium loading, but cytosolic alternans can occur independently.
- Ryanodine receptor 2 (RyR2) dysfunction is a potential alternative mechanism for calcium alternans.
Purpose of the Study:
- To investigate the role of SR release refractoriness in the development of calcium alternans.
- To explore the molecular origins of electromechanical alternans using a computational model of a human atrial cell.
- To elucidate the contribution of RyR2 dynamics to arrhythmogenesis.
Main Methods:
- Developed a mathematical model of a single human atrial cell, modifying RyR2 dynamics and SR calcium release.
- Simulated cellular responses under various pacing rates and RyR2 recovery times.
- Employed S1S2 stimulation protocols to study calcium release restitution and RyR2 refractoriness.
Main Results:
- Cytosolic calcium alternans were observed at fast rates without concurrent SR calcium content fluctuations.
- A transition to alternans was induced by altering RyR2 recovery time, exhibiting hysteresis.
- RyR2 refractoriness, due to slow recovery from inactivation, explained experimental findings on calcium release restitution.
Conclusions:
- RyR2 refractoriness, driven by slow recovery from inactivation, is a key mechanism in the genesis of calcium alternans.
- This study highlights the critical role of RyR2 dysfunction in cardiac alternans and arrhythmogenesis.
- Computational modeling provides insights into the complex dynamics of calcium handling and its link to arrhythmias.
Abstract:
Despite the important role of electromechanical alternans in cardiac arrhythmogenesis, its molecular origin is not well understood. The appearance of calcium alternans has often been associated to fluctuations in the sarcoplasmic reticulum (SR) Ca loading. However, cytosolic calcium alternans observed without concurrent oscillations in the SR Ca content suggests an alternative mechanism related to a dysfunction in the dynamics of the ryanodine receptor (RyR2). We have investigated the effect of SR release refractoriness in the appearance of alternans, using a mathematical model of a single human atrial cell, based on the model by Nygren et al. (30), where we modified the dynamics of the RyR2 and of SR Ca release. The genesis of calcium alternans was studied stimulating the cell for different periods and values of the RyR2 recovery time from inactivation. At fast rates cytosolic calcium alternans were obtained without concurrent SR Ca content fluctuations. A transition from regular response to alternans was also observed, changing the recovery time from inactivation of the RyR2. This transition was found to be hysteretic, so for a given set of parameters different responses were observed. We then studied the relevance of RyR2 refractoriness for the generation of alternans, reproducing the same protocols as in recent experiments. In particular, restitution of Ca release during alternans was studied with a S1S2 protocol, obtaining a different response if the S2 stimulation was given after a long or a short release. We show that the experimental results can be explained by RyR2 refractoriness, arising from a slow RyR2 recovery from inactivation, stressing the role of the RyR2 in the genesis of alternans.
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