- 作者：Marinus A. Borgdorff ; Beatrijs Bartelds ; Michael G. Dickinson ; Paul Steendijk ; Rolf M.F. Berger
- 关键词：Right ventricular failure ; Fibrosis ; Pressure&ndash ; volume loops ; Pulmonary artery banding ; RAAS system ; Maladaptation
- 刊名：International Journal of Cardiology
- 出版年：5 November, 2013
- 年：2013
- 卷：169
- 期：3
- 页码：183-189
- 全文大小：891 K
Background
Right ventricular (RV) failure due to increased pressure load causes significant morbidity and mortality in patients with congenital heart diseases and pulmonary arterial hypertension. It is unknown whether renin-angiotensin-aldosterone-system (RAAS) inhibition (the cornerstone of left ventricular failure treatment) is effective in RV failure. We investigated the effects of combination treatment of aldosterone-blocker eplerenone + angiotensin II receptor blocker losartan (Ep/Lo) on RV remodeling and function in a model of RV failure due to increased pressure load.Methods and results
Rats (n = 48) were randomized for pulmonary artery banding (PAB) or sham surgery and for losartan (20 mg/kg/d) + eplerenone (100 mg/kg/d) treatment (Ep/Lo) or vehicle (VEH). RV function was assessed by echocardiography and pressure-volume analysis at 5 and 11 weeks, or at the occurrence of clinical RV failure symptoms necessitating termination.
PAB resulted in RV failure in all rats, as defined by reduced cardiac output, RV stroke volume, increased RV end diastolic pressure and liver congestion as well as RV fibrosis, hypertrophy and reduced capillary density. Clinical RV failure necessitated termination in 5/12 PAB-VEH rats. Angiotensin II type 1-receptor expression in the RV was reduced in PAB rats indicating local RAAS activation. Treatment of PAB rats with Ep/Lo significantly lowered arterial pressures, but had no significant effect on RV function, remodeling or survival compared to PAB-VEH rats.
Conclusions
RAAS inhibition does not beneficially affect experimental RV failure due to chronic pressure load. This is of high clinical relevance, because it indicates that the RV response to RAAS inhibition might fundamentally differ from that of the LV.