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Updated: Apr 26, 2026

Optical Mapping of Intra-Sarcoplasmic Reticulum Ca2+ and Transmembrane Potential in the Langendorff-perfused Rabbit Heart
Published on: September 10, 2015
Cardiac alternans and intracellular calcium cycling
Joshua N Edwards1, Lothar A Blatter
1Department of Molecular Biophysics and Physiology, Rush University Medical Center, Chicago, IL, USA.
Insights
Cardiac alternans, a beat-to-beat variation in heart cell activity, is linked to arrhythmias. Disturbances in cellular calcium handling are the root cause of this condition.
Area of Science:
- Cardiology
- Cellular Electrophysiology
- Calcium Signaling
Background:
- Cardiac alternans involves beat-to-beat oscillations in electrical activity and contraction strength.
- Clinically, it is associated with cardiac arrhythmias.
- Cellular alternans manifest as alternations in contraction, action potential duration (APD), and calcium transient amplitude.
Purpose of the Study:
- To review the mechanisms underlying cardiac alternans.
- To explore the role of cellular calcium cycling in alternans.
- To discuss the contribution of calcium-handling proteins.
Main Methods:
- Review of existing literature on cardiac alternans.
- Analysis of the bidirectional coupling between membrane voltage and intracellular calcium.
- Focus on cellular calcium handling, including release and reuptake.
Main Results:
- Cardiac alternans originate from disruptions in the voltage-calcium coupling within cardiac cells.
- Disturbances in cellular calcium signaling are the ultimate cause of alternans.
- Key factors include calcium release from internal stores and cytosolic calcium clearance.
Conclusions:
- Cellular calcium cycling dynamics are critical in determining the occurrence of cardiac alternans.
- Understanding calcium handling is essential for addressing alternans and associated arrhythmias.
- Ca(2+) -handling proteins play a significant role in these processes.
Abstract:
Cardiac alternans refers to a condition in which there is a periodic beat-to-beat oscillation in electrical activity and the strength of cardiac muscle contraction at a constant heart rate. Clinically, cardiac alternans occurs in settings that are typical for cardiac arrhythmias and has been causally linked to these conditions. At the cellular level, alternans is defined as beat-to-beat alternations in contraction amplitude (mechanical alternans), action potential duration (APD; electrical or APD alternans) and Ca(2+) transient amplitude (Ca(2+) alternans). The cause of alternans is multifactorial; however, alternans always originate from disturbances of the bidirectional coupling between membrane voltage (Vm ) and intracellular calcium ([Ca(2+) ]i ). Bidirectional coupling refers to the fact that, in cardiac cells, Vm depolarization and the generation of action potentials cause the elevation of [Ca(2+) ]i that is required for contraction (a process referred to as excitation-contraction coupling); conversely, changes of [Ca(2+) ]i control Vm because important membrane currents are Ca(2+) dependent. Evidence is mounting that alternans is ultimately caused by disturbances of cellular Ca(2+) signalling. Herein we review how two key factors of cardiac cellular Ca(2+) cycling, namely the release of Ca(2+) from internal stores and the capability of clearing the cytosol from Ca(2+) after each beat, determine the conditions under which alternans occurs. The contributions from key Ca(2+) -handling proteins (i.e. surface membrane channels, ion pumps and transporters and internal Ca(2+) release channels) are discussed.
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