Eplerenone attenuates pathological pulmonary vascular rather than right ventricular remodeling in pulmonary arterial hypertension

• Published in: BMC pulmonary medicine Vol. 18; no. 1; p. 41
• Main Authors: Boehm, Mario, Arnold, Nadine, Braithwaite, Adam, Pickworth, Josephine, Lu, Changwu, Novoyatleva, Tatyana, Kiely, David G, Grimminger, Friedrich, Ghofrani, Hossein A, Weissmann, Norbert, Seeger, Werner, Lawrie, Allan, Schermuly, Ralph T, Kojonazarov, Baktybek
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 02-03-2018; BioMed Central; BMC
• Subjects: Aldosterone; Animals; Arterial Pressure - drug effects; Care and treatment; Disease Models, Animal; Eplerenone; Eplerenone - pharmacology; Glucocorticoids; Health aspects; Heart; Heart Ventricles - pathology; Hypertension, Pulmonary - drug therapy; Hypertension, Pulmonary - physiopathology; Hypoxia - physiopathology; Male; Mice; Mice, Inbred C57BL; Mineralocorticoid Receptor Antagonists - pharmacology; PAH; Pulmonary Artery - physiopathology; Pulmonary hypertension; Right ventricle; Ventricular Dysfunction, Right - drug therapy; Ventricular Dysfunction, Right - physiopathology; Ventricular Remodeling - drug effects; Eplerenone; PAH; Right ventricle
• ISSN: 1471-2466; 1471-2466
• DOI: 10.1186/s12890-018-0604-x

Aldosterone is a mineralocorticoid hormone critically involved in arterial blood pressure regulation. Although pharmacological aldosterone antagonism reduces mortality and morbidity among patients with severe left-sided heart failure, the contribution of aldosterone to the pathobiology of pulmonary arterial hypertension (PAH) and right ventricular (RV) heart failure is not fully understood.
The effects of Eplerenone (0.1% Inspra® mixed in chow) on pulmonary vascular and RV remodeling were evaluated in mice with pulmonary hypertension (PH) caused by Sugen5416 injection with concomitant chronic hypoxia (SuHx) and in a second animal model with established RV dysfunction independent from lung remodeling through surgical pulmonary artery banding.
Preventive Eplerenone administration attenuated the development of PH and pathological remodeling of pulmonary arterioles. Therapeutic aldosterone antagonism - starting when RV dysfunction was established - normalized mineralocorticoid receptor gene expression in the right ventricle without direct effects on either RV structure (Cardiomyocyte hypertrophy, Fibrosis) or function (assessed by non-invasive echocardiography along with intra-cardiac pressure volume measurements), but significantly lowered systemic blood pressure.
Our data indicate that aldosterone antagonism with Eplerenone attenuates pulmonary vascular rather than RV remodeling in PAH.