Literature DB >> 15134797

The evolution of aldosterone antagonists.

Susan M Garthwaite1, Ellen G McMahon.   

Abstract

Since the isolation and purification of aldosterone from adrenal extracts 50 years ago (Experientia 9 (1953) 33), scientists have learned a great deal about how and where aldosterone acts, the factors that control its release, what is its role in the pathophysiology of cardiovascular disease, how to make and study aldosterone antagonists, and for what medical purposes these agents are useful. In this paper, we will discuss the evolution of aldosterone antagonists from the relatively nonselective spironolactone (Aldactone), to the highly selective eplerenone (Inspra). Eplerenone represents a molecule with improved steroid receptor selectivity and pharmacokinetic properties in man compared to spironolactone. Recent clinical results have demonstrated that these improvements translate into tolerability and efficacy in patients with cardiovascular disease.

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Year:  2004        PMID: 15134797     DOI: 10.1016/j.mce.2003.10.005

Source DB:  PubMed          Journal:  Mol Cell Endocrinol        ISSN: 0303-7207            Impact factor:   4.102


  38 in total

1.  Aldosterone decreases glucose-stimulated insulin secretion in vivo in mice and in murine islets.

Authors:  J M Luther; P Luo; M T Kreger; M Brissova; C Dai; T T Whitfield; H S Kim; D H Wasserman; A C Powers; N J Brown
Journal:  Diabetologia       Date:  2011-04-26       Impact factor: 10.122

Review 2.  Eplerenone: a review of its use in patients with chronic systolic heart failure and mild symptoms.

Authors:  Sohita Dhillon
Journal:  Drugs       Date:  2013-09       Impact factor: 9.546

Review 3.  Mineralocorticoid Receptor Antagonists for Treatment of Hypertension and Heart Failure.

Authors:  Domenic A Sica
Journal:  Methodist Debakey Cardiovasc J       Date:  2015 Oct-Dec

4.  Effects of aldosterone and related steroids on LPS-induced increased expression of inducible NOS in rat aortic smooth muscle cells.

Authors:  V Godfrey; A L Martin; A D Struthers; G A Lyles
Journal:  Br J Pharmacol       Date:  2011-12       Impact factor: 8.739

5.  The XPB Subunit of the TFIIH Complex Plays a Critical Role in HIV-1 Transcription and XPB Inhibition by Spironolactone Prevents HIV-1 Reactivation from Latency.

Authors:  Luisa Mori; Katharine Jenike; Yang-Hui Jimmy Yeh; Benoît Lacombe; Chuan Li; Adam Getzler; Sonia Mediouni; Michael Cameron; Matthew Pipkin; Ya-Chi Ho; Bertha Cecilia Ramirez; Susana Valente
Journal:  J Virol       Date:  2020-11-25       Impact factor: 5.103

6.  A new mode of mineralocorticoid receptor antagonism by a potent and selective nonsteroidal molecule.

Authors:  Jérôme Fagart; Alexander Hillisch; Jessica Huyet; Lars Bärfacker; Michel Fay; Ulrich Pleiss; Elisabeth Pook; Stefan Schäfer; Marie-Edith Rafestin-Oblin; Peter Kolkhof
Journal:  J Biol Chem       Date:  2010-07-22       Impact factor: 5.157

7.  Contrasting effects of eplerenone and spironolactone on adrenal cell steroidogenesis.

Authors:  P Ye; T Yamashita; D M Pollock; H Sasano; W E Rainey
Journal:  Horm Metab Res       Date:  2008-09-25       Impact factor: 2.936

8.  Predicting the relative binding affinity of mineralocorticoid receptor antagonists by density functional methods.

Authors:  Katarina Roos; Anders Hogner; Derek Ogg; Martin J Packer; Eva Hansson; Kenneth L Granberg; Emma Evertsson; Anneli Nordqvist
Journal:  J Comput Aided Mol Des       Date:  2015-11-16       Impact factor: 3.686

9.  Successful effect of triple blockade of renin-angiotensin-aldosterone system on massive proteinuria in a patient with chronic kidney disease.

Authors:  Satoru Kuriyama; Naoki Sugano; Hiroyuki Ueda; Yasushi Otsuka; Go Kanzaki; Tatsuo Hosoya
Journal:  Clin Exp Nephrol       Date:  2009-07-24       Impact factor: 2.801

10.  Short term effects of spironolactone on blood lipid profile: a 3-month study on a cohort of young women with hirsutism.

Authors:  Manouchehr Nakhjavani; Sepehr Hamidi; Alireza Esteghamati; Mehrshad Abbasi; Simindokht Nosratian-Jahromi; Parvin Pasalar
Journal:  Br J Clin Pharmacol       Date:  2009-10       Impact factor: 4.335

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