Mechanisms for the Clinical Benefits of Angiotensin II Receptor Blockers
Author(s) -
R. Schmieder
Publication year - 2005
Publication title -
american journal of hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.009
H-Index - 136
eISSN - 1941-7225
pISSN - 0895-7061
DOI - 10.1016/j.amjhyper.2004.11.032
Subject(s) - medicine , heart failure , blood pressure , angiotensin ii , renin–angiotensin system , blockade , pathophysiology of hypertension , kidney , receptor , endothelial dysfunction , aldosterone , pharmacology , cardiology , angiotensin ii receptor type 1 , angiotensin receptor , endocrinology
The renin-angiotensin-aldosterone system (RAAS) regulates sodium balance, fluid volume, and blood pressure (BP). It is also implicated in the progression of heart failure, hypertension, and kidney disease; this is mediated by the binding of angiotensin II (ang II) to the ang II type 1 but not the ang II type 2 receptor. Preclinical and clinical studies have shown that blockade of the RAAS with ang II receptor blockers (ARB) is effective not only in controlling BP but also in preventing end-organ damage. Through their mechanism of action, ARB may offer benefit with respect to endothelial dysfunction and vascular remodeling, as well as cardiac and renal protection. In addition, both recent and ongoing clinical trials help to clarify further the mechanisms for the benefits of using ARB across the cardiovascular continuum.
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