The Mechanisms of Actions of Aldosterone and its Antagonists in Cardiovascular Disease
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Published:2019-04-26
Issue:46
Volume:24
Page:5491-5499
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ISSN:1381-6128
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Container-title:Current Pharmaceutical Design
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language:en
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Short-container-title:CPD
Author:
Pantelidis Panteleimon1, Sideris Michail2, Viigimaa Margus3, Avranas Konstantinos1, Deligkaris Pavlos1, Zografou Ioanna1, Lovic Dragan4
Affiliation:
1. 2nd Propaedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece 2. Women Health Research Unit, Queen Mary University of London, London, United Kingdom 3. Centre of Cardiology, North Estonia Medical Centre, Tallinn, Estonia; Institute of Health Technologies, Tallinn University of Technology, Tallinn, Estonia 4. Clinic for Internal Disease Intermedica, Cardiology department, Hypertension Center, Nis, Serbia
Abstract
Background:
Aldosterone, through its actions on Mineralcorticosteroid Receptors (MR), controls fluid
and electrolyte balance, but also exerts various direct deleterious actions on the vasculature. A number of aldosterone
antagonists have been manufactured to reverse these effects.
Objective:
A comprehensive review of the underlying mechanisms of the actions of aldosterone and its antagonists
in cardiovascular disease.
Method:
The relevant studies indexed in PubMed, Scopus and Google Scholar databases, published from 2003 to
May 2018 were identified and reported.
Results:
Aldosterone binds to MR, activating them as intracellular transcription factors. Moreover, aldosterone,
through its actions on MR, as well as on another not fully explored class of receptors, triggers several signaling
pathways that produce rapid, non-genomic actions. In the vasculature, all these changes favor the establishment of
inflammation and cardiovascular dysfunction, which, in turn, lead to or exacerbate various cardiovascular diseases.
Mineralcorticosteroid Antagonists (MRA) are compounds that antagonize the action of aldosterone on MR.
Spironolactone was the first steroidal MRA to be commercially used. It showed beneficial clinical results, but
also a number of adverse effects. The next generation of steroidal MRA, exhibited lower potency but did not
induce many of these adverse reactions, due to their high selectivity for MR. The third generation of MRA compromises
the newly introduced non-steroidal MRA, which have a completely different chemical structure, they
induce different and more drastic changes to MR, they are much more specific and currently under clinical trials.
Conclusion:
New MRA, which block the aldosterone induced pathways in the vasculature, hold promising results
for the treatment of cardiovascular disease.
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology
Reference46 articles.
1. Coghlan J, Tait JF. , Aldosterone: History and introduction Textbook of nephro-endocrinology, , 2009 2. Williams GH. Heart Fail Rev, Aldosterone biosynthesis, regulation, and classical mechanism of action., 2005, 10, 7-13, 3. Arai K, Chrousos GP. , Aldosterone Deficiency and Resistance. In:De Groot LJ, Chrousos G, Dungan K, et al., Eds. Endotext. South Dartmouth (MA): MDText.com, Inc, , 2000 4. Markowitz M, Messineo F, Coplan NL. Clin Cardiol, Aldosterone receptor antagonists in cardiovascular disease: A review of the recent literature and insight into potential future indications., 2012, 35, 605-609, 5. Gajjala PR, Sanati M, Jankowski J. Front Immunol, Cellular and molecular mechanisms of chronic kidney disease with diabetes mellitus and cardiovascular diseases as its comorbidities., 2015, 6, 340-,
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