Document Detail


Aldosterone and its blockade: a cardiovascular and renal perspective.
MedLine Citation:
PMID:  16604252     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Aldosterone not only contributes to salt and water homeostasis, but also exerts direct cardiovascular and renal effects. Numerous experimental and clinical studies indicate that aldosterone participate in cardiac alterations associated with hypertension, heart failure, diabetes and other pathological entities. It is important to mention that dietary salt is a key factor in aldosterone-mediated cardiovascular damage, since damage was more evident in animals on a high-salt diet than animals on a low salt diet. A pathophysiological action of aldosterone involves development of extracellular matrix and fibrosis, inflammation, stimulation of reactive oxygen species production, endothelial dysfunction, cell growth and proliferation. Many studies showed local extra-adrenal production of aldosterone in brain blood vessel, and the heart, which contribute in an important manner to the pathological actions of this mineralocorticoid. Several studies such as RALES, EPHESUS, 4E and others, recently showed that mineralocorticoid-receptor (MR) antagonists, alone or in combination with ACE inhibitors or ARBs, reduced the risk of progressive target organ damage and hospitalization in patients with hypertension and heart failure. These clinical benefits support the therapeutic usefulness of MR antagonists.
Authors:
V Lahera; V Cachofeiro; G Balfagon; J L Rodicio
Publication Detail:
Type:  Journal Article; Review     Date:  2006-04-03
Journal Detail:
Title:  TheScientificWorldJournal     Volume:  6     ISSN:  1537-744X     ISO Abbreviation:  ScientificWorldJournal     Publication Date:  2006  
Date Detail:
Created Date:  2006-04-10     Completed Date:  2006-05-03     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  101131163     Medline TA:  ScientificWorldJournal     Country:  England    
Other Details:
Languages:  eng     Pagination:  413-24     Citation Subset:  IM    
Affiliation:
Department of Physiology, School of Medicine, Universidad Complutense, Madrid, Spain.
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MeSH Terms
Descriptor/Qualifier:
Aldosterone / physiology*
Aldosterone Antagonists / pharmacology*
Cardiovascular Physiological Phenomena*
Heart Diseases / physiopathology
Humans
Kidney / physiology*
Kidney Diseases / physiopathology
Receptors, Aldosterone / physiology*
Receptors, Mineralocorticoid / physiology
Chemical
Reg. No./Substance:
0/Aldosterone Antagonists; 0/Receptors, Aldosterone; 0/Receptors, Mineralocorticoid; 52-39-1/Aldosterone

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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