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TRPM4 Participates in Aldosterone-Salt-Induced Electrical Atrial Remodeling in Mice.

Authors :
Simard C
Ferchaud V
Sallé L
Milliez P
Manrique A
Alexandre J
Guinamard R
Source :
Cells [Cells] 2021 Mar 12; Vol. 10 (3). Date of Electronic Publication: 2021 Mar 12.
Publication Year :
2021

Abstract

Aldosterone plays a major role in atrial structural and electrical remodeling, in particular through Ca <superscript>2+</superscript> -transient perturbations and shortening of the action potential. The Ca <superscript>2+</superscript> -activated non-selective cation channel Transient Receptor Potential Melastatin 4 (TRPM4) participates in atrial action potential. The aim of our study was to elucidate the interactions between aldosterone and TRPM4 in atrial remodeling and arrhythmias susceptibility. Hyperaldosteronemia, combined with a high salt diet, was induced in mice by subcutaneously implanted osmotic pumps during 4 weeks, delivering aldosterone or physiological serum for control animals. The experiments were conducted in wild type animals ( Trpm4 <superscript>+/+</superscript> ) as well as Trpm4 knock-out animals ( Trpm4 <superscript>-/-</superscript> ). The atrial diameter measured by echocardiography was higher in Trpm4 <superscript>-/-</superscript> compared to Trpm4 <superscript>+/+</superscript> animals, and hyperaldosteronemia-salt produced a dilatation in both groups. Action potentials duration and triggered arrhythmias were measured using intracellular microelectrodes on the isolated left atrium. Hyperaldosteronemia-salt prolong action potential in Trpm4 <superscript>-/-</superscript> mice but had no effect on Trpm4 <superscript>+/+</superscript> mice. In the control group (no aldosterone-salt treatment), no triggered arrythmias were recorded in Trpm4 <superscript>+/+</superscript> mice, but a high level was detected in Trpm4 <superscript>-/-</superscript> mice. Hyperaldosteronemia-salt enhanced the occurrence of arrhythmias (early as well as delayed-afterdepolarization) in Trpm4 <superscript>+/+</superscript> mice but decreased it in Trpm4 <superscript>-/-</superscript> animals. Atrial connexin43 immunolabelling indicated their disorganization at the intercalated disks and a redistribution at the lateral side induced by hyperaldosteronemia-salt but also by Trpm4 disruption. In addition, hyperaldosteronemia-salt produced pronounced atrial endothelial thickening in both groups. Altogether, our results indicated that hyperaldosteronemia-salt and TRPM4 participate in atrial electrical and structural remodeling. It appears that TRPM4 is involved in aldosterone-induced atrial action potential shortening. In addition, TRPM4 may promote aldosterone-induced atrial arrhythmias, however, the underlying mechanisms remain to be explored.

Details

Language :
English
ISSN :
2073-4409
Volume :
10
Issue :
3
Database :
MEDLINE
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
33809210
Full Text :
https://doi.org/10.3390/cells10030636