Literature DB >> 19427273

Aldosterone blockade attenuates development of an electrophysiological substrate associated with ventricular tachyarrhythmias in heart failure.

Bruce S Stambler1, Kenneth R Laurita, Sunil C Shroff, Gregory Hoeker, Nichole L Martovitz.   

Abstract

BACKGROUND: Aldosterone blockade reduces sudden cardiac death in heart failure, but the underlying mechanism is unclear.
OBJECTIVE: This study's aim was to determine whether chronic eplerenone treatment protects against detrimental ventricular electrical remodeling and development of an arrhythmogenic substrate in a rapid ventricular pacing (RVP)-induced heart failure model.
METHODS: Dogs were assigned randomly to oral placebo or eplerenone treatment and divided into 4 groups: 2 sham-operated (no RVP) and 2 RVP groups. After 5 weeks of no RVP or RVP along with concurrent placebo or eplerenone treatment, dogs underwent echocardiographic assessments of systolic function and chamber size and electrophysiologic measurements of ventricular repolarization, refractoriness, conduction, tachyarrhythmia inducibility, and myocardial activation delays after premature stimulation.
RESULTS: Eplerenone failed to prevent left ventricular systolic dysfunction or chamber enlargement in RVP dogs. Eplerenone attenuated prolongation of ventricular repolarization and refractoriness, increases in dispersion of repolarization and refractoriness, fractionation of ventricular electrograms, and delays in myocardial activation after premature stimulation at short coupling intervals and improved arrhythmia vulnerability score in RVP dogs with heart failure. Ventricular tachyarrhythmia inducibility in heart failure dogs was predicted by activation delays after premature stimulation at short coupling intervals, which were prevented by eplerenone. Eplerenone did not alter electrophysiological parameters in no-RVP dogs without heart failure.
CONCLUSIONS: Eplerenone attenuates heart failure-related ventricular electrical remodeling and tachyarrhythmia vulnerability. Inhibition of myocardial activation delays during premature excitation may contribute to preventing development of an arrhythmogenic ventricular substrate in heart failure.

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Year:  2009        PMID: 19427273     DOI: 10.1016/j.hrthm.2009.02.005

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  4 in total

Review 1.  [New developments in the antiarrhythmic therapy of atrial fibrillation].

Authors:  H Simon; K Simon Demel; G Ritscher; O Turschner; J Brachmann
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2010-12

2.  Effects of mineralocorticoid receptor antagonists on the risk of sudden cardiac death in patients with left ventricular systolic dysfunction: a meta-analysis of randomized controlled trials.

Authors:  Srinivas R Bapoje; Amit Bahia; John E Hokanson; Pamela N Peterson; Paul A Heidenreich; Joann Lindenfeld; Larry A Allen; Frederick A Masoudi
Journal:  Circ Heart Fail       Date:  2013-02-12       Impact factor: 8.790

3.  Effect of spironolactone on ventricular arrhythmias in patients with left ventricular systolic dysfunction and implantable cardioverter defibrillators.

Authors:  Abdul Wase; Naga Garikipati; Omar Mufti; Zulfiqar Mirza; Aparna Innaparthy; Anwarul Kabir; Mohammed B Quraishi; Ronald Markert
Journal:  Indian Heart J       Date:  2012-04-28

4.  Rapid and MR-Independent IK1 Activation by Aldosterone during Ischemia-Reperfusion.

Authors:  Joachim Alexandre; Thomas Hof; Paolo Emilio Puddu; René Rouet; Romain Guinamard; Alain Manrique; Farzin Beygui; Laurent Sallé; Paul Milliez
Journal:  PLoS One       Date:  2015-07-29       Impact factor: 3.240

  4 in total

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