Calcium signalling silencing in atrial fibrillation

Maura Greiser1

  • 1Center for Biomedical Engineering and Technology and Department of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.

Insights

Subcellular calcium signalling silencing is an adaptive response to rapid heart activation during atrial fibrillation (AF). This mechanism reduces calcium instability and arrhythmogenicity, offering a protective effect against AF progression.

Area of Science:

  • Cardiology
  • Cellular Biology
  • Molecular Biology

Background:

  • Rapid cardiac activation, as seen in paroxysmal atrial fibrillation (AF), triggers cellular responses.
  • Intracellular calcium (Ca2+) signalling instability contributes to arrhythmogenicity in AF.
  • Understanding adaptive responses is crucial for managing AF.

Purpose of the Study:

  • To investigate subcellular calcium signalling silencing as a novel adaptive response to rapid cardiac activation in AF.
  • To elucidate the molecular mechanisms and functional consequences of calcium signalling silencing in AF.

Main Methods:

  • Analysis of subcellular calcium signalling in patients with AF and a rabbit model.
  • Assessment of calcium release channel (ryanodine receptor, RyR2) expression levels.
  • Measurement of Ca2+ sparks, arrhythmogenic Ca2+ waves, action potentials, and L-type Ca2+ current.

Main Results:

  • Calcium signalling silencing was observed in patients with AF and a rabbit model, characterized by failed Ca2+ signal propagation.
  • This adaptive response significantly reduced ryanodine receptor (RyR2) expression and the frequency of Ca2+ sparks and waves.
  • Key features include reduced Ca2+ release, enhanced Ca2+ buffering, shortened action potentials, and decreased intracellular Na+.

Conclusions:

  • Calcium signalling silencing is a distinct anti-arrhythmic adaptive mechanism counteracting Ca2+-based arrhythmogenicity in AF.
  • This process limits the pro-arrhythmic role of unstable Ca2+ signalling during AF.
  • The AF Ca2+ signalling phenotype results from a balance between stabilizing (silencing) and destabilizing factors.

Related Concept Videos

Antihypertensive Drugs: Action of Calcium Channel Blockers01:18

Antihypertensive Drugs: Action of Calcium Channel Blockers

Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
2.0K
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
2.5K
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of...
2.8K
Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
6.8K
Feedback Regulation of Calcium Concentration01:27

Feedback Regulation of Calcium Concentration

Calcium is an essential signaling molecule required for various cellular functions. Calcium pumps and ion channels on cell and organellar membranes, such as those on the endoplasmic reticulum (ER), regulate calcium concentrations inside the cell. They remain closed, keeping the cytosolic calcium levels low at a resting state.
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
4.1K
Mechanism of Cardiac Arrhythmias01:28

Mechanism of Cardiac Arrhythmias

Arrhythmias are irregular heart rhythms occurring when the heart's electrical impulses become abnormal. These disturbances can lead to various symptoms, depending on their severity and the underlying cause. Some common factors contributing to arrhythmias include hypoxia, ischemia, electrolyte imbalances, excessive catecholamine exposure, drug toxicity, and muscle overstretching. Arrhythmias can be classified into two main types based on the rate and site of origin of abnormal heart rhythms.
2.5K