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Cardiac dopamine D1 receptor triggers ventricular arrhythmia in chronic heart failure.

Toshihiro YamaguchiTomokazu S SumidaSeitaro NomuraMasahiro SatohTomoaki HigoMasamichi ItoToshiyuki KoKanna FujitaMary E SweetAtsushi SanbeKenji YoshimiIchiro ManabeToshikuni SasaokaMatthew R G TaylorHaruhiro TokoEiki TakimotoAtsuhiko T NaitoIssei Komuro
Published in: Nature communications (2020)
Pathophysiological roles of cardiac dopamine system remain unknown. Here, we show the role of dopamine D1 receptor (D1R)-expressing cardiomyocytes (CMs) in triggering heart failure-associated ventricular arrhythmia. Comprehensive single-cell resolution analysis identifies the presence of D1R-expressing CMs in both heart failure model mice and in heart failure patients with sustained ventricular tachycardia. Overexpression of D1R in CMs disturbs normal calcium handling while CM-specific deletion of D1R ameliorates heart failure-associated ventricular arrhythmia. Thus, cardiac D1R has the potential to become a therapeutic target for preventing heart failure-associated ventricular arrhythmia.
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