2005Mini-Reviews in Medicinal ChemistryRequires access

Molecular Mechanisms of Mineralocorticoid Receptor Antagonism by Eplerenone

Xiao Hu, Suzhen Li, Ellen McMahon, Deepak Anil Lala, Amy E. Rudolph

Open publisher page 41 citations

Abstract

Mineralocorticoid receptor (MR) antagonism has proven to effectively attenuate the pathophysiological effects of aldosterone in clinical and experimental settings of hypertension and heart failure. MR activates transcription of target genes upon aldosterone binding, and eplerenone selectively binds to MR and blocks aldosterone- mediated activation. In this review, we summarize the preclinical and clinical evidence supporting the beneficial effects of eplerenone (INSPRATM), a selective aldosterone blocker, in the treatment of hypertension and heart failure. We also review the current status in understanding the molecular mechanisms of action of the MR and its ligand. In addition, we compare the effects of eplerenone and spironolactone, a nonselective aldosterone blocker, on the transcriptional activity of MR and provide a molecular explanation for the improved side-effect profile of eplerenone compared with spironolactone. Keywords: hypertension, reninangiotensin-aldosterone system, angiotensin-converting enzyme, aldosterone antagonist., antihypertensive, histone acetyltransferase, cortical collecting tubule

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Mineralocorticoid receptor (MR) antagonism has proven to effectively attenuate the pathophysiological effects of aldosterone in clinical and experimental settings of hypertension and heart failure. MR activates transcription of target genes upon aldosterone binding, and eplerenone selectively binds to MR and blocks aldosterone- mediated activation. In this review, we summarize the preclinical and clinical evidence supporting the beneficial effects of eplerenone (INSPRATM), a selective aldosterone blocker, in the treatment of hypertension and heart failure. We also review the current status in understanding the molecular mechanisms of action of the MR and its ligand. In addition, we compare the effects of eplerenone and spironolactone, a nonselective aldosterone blocker, on the transcriptional activity of MR and provide a molecular explanation for the improved side-effect profile of eplerenone compared with spironolactone. Keywords: hypertension, reninangiotensin-aldosterone system, angiotensin-converting enzyme, aldosterone antagonist., antihypertensive, histone acetyltransferase, cortical collecting tubule

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Available abstract

Mineralocorticoid receptor (MR) antagonism has proven to effectively attenuate the pathophysiological effects of aldosterone in clinical and experimental settings of hypertension and heart failure. MR activates transcription of target genes upon aldosterone binding, and eplerenone selectively binds to MR and blocks aldosterone- mediated activation. In this review, we summarize the preclinical and clinical evidence supporting the beneficial effects of eplerenone (INSPRATM), a selective aldosterone blocker, in the treatment of hypertension and heart failure. We also review the current status in understanding the molecular mechanisms of action of the MR and its ligand. In addition, we compare the effects of eplerenone and spironolactone, a nonselective aldosterone blocker, on the transcriptional activity of MR and provide a molecular explanation for the improved side-effect profile of eplerenone compared with spironolactone. Keywords: hypertension, reninangiotensin-aldosterone system, angiotensin-converting enzyme, aldosterone antagonist., antihypertensive, histone acetyltransferase, cortical collecting tubule

Key concepts: Eplerenone, Mineralocorticoid receptor, Antagonism, Mineralocorticoid, Spironolactone, Endocrinology, Internal medicine, Pharmacology

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