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.

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