Abstract
Background Dilated cardiomyopathy (DCM) is a leading cause of heart failure, with 30–50 % of cases attributed to familial inheritance. Mutations in RNA-binding motif protein 20 (RBM20) account for 3–5 % of cases and are associated with severe DCM and ventricular arrhythmias. However, the role of RBM20 mutations in atrial cardiomyopathy (AtCM) and atrial fibrillation (AF) remains underexplored. This study investigates the effects of the RBM20-R636Q mutation on atrial electrophysiology and evaluates sodium-glucose co-transporter (SGLT) inhibitors as potential therapeutics.
Results
Rbm20-R636Q mice exhibited atrial remodeling, including hypertrophy, left atrial enlargement, and shortened action potential duration at 90% repolarization (APD90). Compared with RBM20-knockout and laminopathy models, RBM20-R636Q mice showed distinct reductions in Ito / IKur without changes in IK,sus or IK,tail currents, alongside TASK-1 potassium current upregulation and alterations of ICaL. SGLT inhibitors (sotagliflozin, empagliflozin, dapagliflozin) reduced AP inducibility and partially restored APD90, with effects comparable to lidocaine, suggesting a role in modulating peak sodium currents.
Conclusions
RBM20 mutations contribute to atrial remodeling, promoting AtCM and AF. SGLT inhibitors demonstrate therapeutic potential by modulating atrial electrophysiology and reducing arrhythmogenesis, offering a promising strategy for managing RBM20-related cardiac disorders.
Competing Interest Statement
The authors have declared no competing interest.
Non-standard Abbreviations and Acronyms
- AF
- atrial fibrillation
- AP
- action potential
- APD
- action potential duration
- AtCM
- atrial cardiomyopathy
- CaMKIIδ
- Calcium/Calmodulin-dependent protein kinase II delta
- CM
- cardiomyocyte
- DCM
- dilated cardiomyopathy
- DMSO
- dimethyl sulfoxide
- ECG
- electrocardiogram
- EGTA
- ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
- ES
- embryonic stem
- FVB
- Friend leukemia virus B strain
- GEO
- Gene Expression Omnibus
- GWAS
- genome-wide association studies
- HEPES
- 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid
- KO
- knockout
- LA
- left atrium
- LV
- left ventricle
- MOPS
- 3-morpholinopropane-1-sulfonic acid
- RS
- arginine-serine
- SGLT
- sodium-glucose co-transporter
- SGLTi
- sodium-glucose cotransporter inhibitors
- SNP
- single nucleotide polymorphism
- TEA-Cl
- tetraethylammonium chloride
- TTN
- titin
- WT
- wild-type
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