Piglet Model of Chronic Pulmonary Hypertension. (1st December 2013)

• Record Type: Journal Article
• Authors: Mercier, Olaf; Tivane, Adriano; Dorfmüller, Peter; de Perrot, Marc; Raoux, François; Decante, Benoît; Eddahibi, Saadia; Dartevelle, Philippe; Fadel, Elie
• Is Part Of: Pulmonary circulation. Volume 3:Number 4(2013)
• Page Start: 908
• Page End: 915
• Publication Date: 2013-12-01
• Subjects: chronic thromboembolic pulmonary hypertension -- pulmonary hypertension -- animal model; Pulmonary circulation -- Periodicals; Pulmonary circulation; Electronic journals -- Sciences; Periodicals; 616.24005
• DOI: 10.1086/674757
• Languages: English
• ISSNs: 2045-8932

Abstract

Abstract : None of the animal models have been able to reproduce all aspects of CTEPH because of the rapid resolution of the thrombi in the pulmonary vasculature. The aim of this study was to develop an easily reproducible large‐animal model of chronic pulmonary hypertension (PH) related to the development of a postobstructive and overflow vasculopathy. Chronic PH was induced in 5 piglets by ligation of the left pulmonary artery (PA) through a midline sternotomy followed by weekly transcatheter embolization of the right lower‐lobe arteries. Sham‐operated piglets ( n = 5) served as controls. Hemodynamics, RV function, lung morphometry, and endothelin‐1 (ET‐1) pathway gene expression (ET‐1 and its receptors ETA and ETB) were assessed after 5 weeks in the obstructed (left lung and right lower lobe) and unobstructed (right upper lobe) territories. All animals developed chronic PH within 5 weeks. Compared to controls, chronic‐PH animals had higher mean PA pressure (28.5 ± 1.7 vs. 11.6 ± 1.8 mmHg, P = 0.0001) and total pulmonary resistance (784 ± 160 vs. 378 ± 51 dyn s −1 cm −5, P = 0.05). Echocardiography showed RV enlargement, RV wall thickening (56 ± 5 vs. 30 ± 4 mm, P = 0.0003), decreased tricuspid annular plane systolic excursion (11.3 ± 0.9 vs. 14.4 ± 0.4 mm, P = 0.01), and paradoxical septal motion. In obstructed territories, morphometry demonstrated increases in the number of bronchial arteries per bronchus (8.7 ± 0.9 vs. 2 ± 0.17, P < 0.0001) and in distal PA media thickness (60% ± 2.8% vs. 29% ± 0.9%, P < 0.0001), consistent with postobstructive vasculopathy. Distal PA media thickness was increased in unobstructed territories (70% ± 2.4% vs. 29% ± 0.9%, P < 0.0001). ET‐1 was overexpressed in unobstructed territories, compared to controls and obstructed territories. In conclusion, the large‐animal model described here is reproducible and led to the development of PH in a relatively short time frame.