Unknown

Dataset Information

0

Conditional mineralocorticoid receptor expression in the heart leads to life-threatening arrhythmias.


ABSTRACT: Life-threatening cardiac arrhythmia is a major source of mortality worldwide. Besides rare inherited monogenic diseases such as long-QT or Brugada syndromes, which reflect abnormalities in ion fluxes across cardiac ion channels as a final common pathway, arrhythmias are most frequently acquired and associated with heart disease. The mineralocorticoid hormone aldosterone is an important contributor to morbidity and mortality in heart failure, but its mechanisms of action are incompletely understood.To specifically assess the role of the mineralocorticoid receptor (MR) in the heart, in the absence of changes in aldosteronemia, we generated a transgenic mouse model with conditional cardiac-specific overexpression of the human MR. Mice exhibit a high rate of death prevented by spironolactone, an MR antagonist used in human therapy. Cardiac MR overexpression led to ion channel remodeling, resulting in prolonged ventricular repolarization at both the cellular and integrated levels and in severe ventricular arrhythmias.Our results indicate that cardiac MR triggers cardiac arrhythmias, suggesting novel opportunities for prevention of arrhythmia-related sudden death.

SUBMITTER: Ouvrard-Pascaud A 

PROVIDER: S-EPMC3635833 | biostudies-literature | 2005 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


<h4>Background</h4>Life-threatening cardiac arrhythmia is a major source of mortality worldwide. Besides rare inherited monogenic diseases such as long-QT or Brugada syndromes, which reflect abnormalities in ion fluxes across cardiac ion channels as a final common pathway, arrhythmias are most frequently acquired and associated with heart disease. The mineralocorticoid hormone aldosterone is an important contributor to morbidity and mortality in heart failure, but its mechanisms of action are in  ...[more]

Similar Datasets

| S-EPMC3075419 | biostudies-literature
| S-EPMC8139815 | biostudies-literature
| S-EPMC8207167 | biostudies-literature
| S-EPMC9707810 | biostudies-literature
| S-EPMC124545 | biostudies-literature
| S-EPMC3256134 | biostudies-literature
| S-EPMC4845125 | biostudies-other
| S-EPMC6748747 | biostudies-literature
| S-EPMC8677441 | biostudies-literature
| S-EPMC9039676 | biostudies-literature