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Published on: July 14, 2021
Molecular mechanisms of myocardial remodeling. The role of aldosterone
Claude Delcayre1, Bernard Swynghedauw
1CD Directeur de Recherches au CNRS, U217-INSERM, Hôpital Lariboisière, Paris, France.
Insights
Aldosterone contributes to cardiac remodeling and fibrosis, particularly after myocardial infarction and in heart failure. Blocking aldosterone, for example with spironolactone, reduces fibrosis and improves outcomes.
Area of Science:
- Cardiovascular Physiology
- Molecular Cardiology
- Evolutionary Medicine
Background:
- Cardiac remodeling (CR) is influenced by mechanical stress, aging, and neurohormonal factors.
- Aldosterone plays a key role in cardiovascular fibrosis, especially with high sodium intake.
- Aldosterone's effects are mediated through its receptor, influencing gene expression and fibrosis pathways.
Purpose of the Study:
- To explore the role of aldosterone in cardiac remodeling and fibrosis.
- To investigate the mechanisms of aldosterone-induced cardiac fibrosis.
- To examine the impact of aldosterone production in myocardial infarction and heart failure.
Main Methods:
- Review of evidence on aldosterone's role in cardiovascular system.
- Analysis of aldosterone receptor pathways and gene expression.
- Examination of clinical trial data (e.g., RALES) and animal studies on myocardial infarction and heart failure models.
Main Results:
- Aldosterone induces fibrosis throughout the cardiovascular system, potentiated by high sodium diets.
- Aldosterone upregulates angiotensin II type I and glucocorticoid receptors.
- Spironolactone demonstrated significant benefits in heart failure, linked to reduced fibrosis.
- Intracardiac aldosterone production occurs, regulated by diet and angiotensin II, and is elevated post-myocardial infarction and in heart failure.
Conclusions:
- Local aldosterone and angiotensin II production are critical in regulating fibrosis after myocardial infarction.
- Activated aldosterone production, both adrenal and cardiac, contributes detrimentally to fibrosis during heart failure as part of the neurohormonal response.
Abstract:
Cardiac remodeling, CR, is a complex and rather controversial issue and results from the, sometimes opposite, trophic effects of pure mechanical overload, and susceptibility factors, as senescence, aetiologies, as ischemia, and the neurohormonal reaction. The molecular mechanisms of CR are heritable and had, in the past, increased fitness, as such CR belongs to evolutionary medicine. Aldosterone production plays an important role in the remodeling of the heart. (i) There are numerous evidences that aldosterone induces fibrosis in all the cardiovascular system in the presence of high sodium diet. The aldosterone receptor is a transcriptional factor and the pathways that lead to aldosterone-induced fibrosis are multiple. Aldosterone induces the expression of the angiotensin II receptors subtype I and that of the glucocorticoid receptors. The RALES trial have recently evidenced a significant beneficial effect of spironolactone on both mortality and morbidity in heart failure, and a substudy has shown that these effects are linked to a reduction is fibrosis. (ii) An intracardiac production of aldosterone and corticosterone have been evidenced in the rat. Aldosterone production is regulated by low sodium/high potassium diets and by angiotensin II and is predominant in atria, cardiac production is low as compared to the adrenal production, nevertheless it results in high local concentrations, just like angiotensin II. In rats, myocardial infarction activates aldosterone production and this activation is prevented by losartan. Heart failure, in human, activates aldosterone production and is accompanied by a significant increase of the arteriovenous difference in aldosterone by the myocardium. To conclude (i) after a myocardial infarction local production of aldosterone and angiotensin II are likely to play a major role in regulating collagen turnover and fibrous tissue formation; (ii) during heart failure, the activation of adrenal and cardiovascular production of aldosterone belongs to the neurohormonal reaction and would play a detrimental role in producing reactive fibrosis.
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