Estrogen rescues preexisting severe pulmonary hypertension in rats

• Published in: American journal of respiratory and critical care medicine Vol. 184; no. 6; pp. 715 - 723
• Main Authors: Umar, Soban, Iorga, Andrea, Matori, Humann, Nadadur, Rangarajan D, Li, Jingyuan, Maltese, Federica, van der Laarse, Arnoud, Eghbali, Mansoureh
• Format: Journal Article
• Language: English
• Published: United States American Thoracic Society 15.09.2011
• Subjects: Angiogenesis; Animals; Blood Pressure - drug effects; Blotting, Western; Estradiol - administration & dosage; Estrogens; Estrogens - therapeutic use; Females; Heart - drug effects; Hypertension, Pulmonary - drug therapy; Investigations; Laboratory animals; Lungs; Male; Polymerase chain reaction; Pulmonary arteries; Pulmonary Artery - drug effects; Pulmonary hypertension; Rats; Rats, Sprague-Dawley; Real-Time Polymerase Chain Reaction; Severity of Illness Index
• ISSN: 1073-449X; 1535-4970
• DOI: 10.1164/rccm.201101-0078OC

Pulmonary hypertension (PH) is characterized by progressive increase in pulmonary artery pressure leading to right ventricular (RV) hypertrophy, RV failure, and death. Current treatments only temporarily reduce severity of the disease, and an ideal therapy is still lacking. Estrogen pretreatment has been shown to attenuate development of PH. Because PH is not often diagnosed early, we examined if estrogen can rescue preexisting advanced PH. PH was induced in male rats with monocrotaline (60 mg/kg). At Day 21, rats were either treated with 17-β estradiol or estrogen (E2, 42.5 μg/kg/d), estrogen receptor-β agonist (diarylpropionitrile, 850 μg/kg/d), or estrogen receptor α-agonist (4,4',4"-[4-Propyl-(1H)-pyrazole-1,3,5-triyl] trisphenol, 850 μg/kg/d) for 10 days or left untreated to develop RV failure. Serial echocardiography, cardiac catheterization, immunohistochemistry, Western blot, and real-time polymerase chain reaction were performed. Estrogen therapy prevented progression of PH to RV failure and restored lung and RV structure and function. This restoration was maintained even after removal of estrogen at Day 30, resulting in 100% survival at Day 42. Estradiol treatment restored the loss of blood vessels in the lungs and RV. In the presence of angiogenesis inhibitor TNP-470 (30 mg/kg) or estrogen receptor-β antagonist (PHTPP, 850 μg/kg/d), estrogen failed to rescue PH. Estrogen receptor-β selective agonist was as effective as estrogen in rescuing PH. Estrogen rescues preexisting severe PH in rats by restoring lung and RV structure and function that are maintained even after removal of estrogen. Estrogen-induced rescue of PH is associated with stimulation of cardiopulmonary neoangiogenesis, suppression of inflammation, fibrosis, and RV hypertrophy. Furthermore, estrogen rescue is likely mediated through estrogen receptor-β.