RYR2 as new target for antiarrhythmic therapy: Harnessing the power of existing chemical entities for drug discovery
Year: 2025
Type: article
Abstract: The intracellular calcium release channel ryanodine receptor type 2 (RyR2) plays an essential role in the cardiac excitation-contraction coupling. Hyperactive RyR2 calcium channels caused by gain-of-function mutations or posttranslational modifications in structural heart disease have been linked to atrial and ventricular arrhythmias. We review new RyR2 inhibitors and their use as antiarrhythmic drugs in animal models of ventricular arrhythmias.
Source: Heart Rhythm
Authors: Tri Q. Do, Björn C. Knollmann
Institutions: Vanderbilt University, Vanderbilt University Medical Center
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,790
OpenAlex ID: W4409953215
