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Pulmonary hypertension after pneumonectomy: a preclinical model in rats and human pulmonary endothelial cells

Title: Pulmonary hypertension after pneumonectomy: a preclinical model in rats and human pulmonary endothelial cells
Authors: Sentenac, Pierre; Samarani, Gianluca; Bideaux, Patrice; Sicard, Pierre; Bourdois, Benjamin; Richard, Sylvain; Colson, Pascal H; Eddahibi, Saadia
Contributors: institutional and/or departmental sources
Source: European Journal of Cardio-Thoracic Surgery ; volume 59, issue 1, page 147-154 ; ISSN 1010-7940 1873-734X
Publisher Information: Oxford University Press (OUP)
Publication Year: 2020
Description: OBJECTIVES Pulmonary hypertension and heart disease contribute to the high morbidity rate following pneumonectomy (PN). The pathophysiology is still poorly understood. The objective was to investigate the consequences of PN on cardiopulmonary function in rats and to explore in vitro the involved mechanisms. METHODS Sixty Sprague-Dawley male rats randomly underwent either a right PN (PN group) or sham surgery. Ten rats per group were sacrificed on postoperative days 3, 7 and 28. Cardiopulmonary alterations were investigated by echocardiographic, haemodynamic and histological analyses. In vitro, the shear stress was reproduced using a Flexcell Tension™ cyclic stretch on cultured human pulmonary endothelial cells (P-ECs) to investigate the impact on pulmonary artery smooth muscle cell (PA-SMC) growth. Data are expressed as mean ± SD. RESULTS Mean pulmonary arterial pressure gradually increased in the PN group to reach 35 ± 7 mmHg on postoperative day 28 vs 18 ± 4 in sham (P = 0.001), likewise the proportion of muscularized distal pulmonary arteries, 83 ± 1% vs 5 ± 1%, respectively (P < 0.001), related to in situ PA-SMC proliferation. The right ventricle area and lateral wall thickness were doubled in the PN group on postoperative day 28. The left ventricle ejection fraction decreased on postoperative days 7 and 28 while the right ventricle function was maintained. In vitro, the human PA-SMC growth was significantly greater when seeded with stretched vs non-stretched P-EC media, highlighting the role of shear stress on the P-EC paracrine function. CONCLUSIONS Right PN led to pulmonary hypertension and proportional right heart remodelling in rats. The shear stress related to high blood flow alters the pulmonary endothelial paracrine control of SMC growth.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/ejcts/ezaa277
Availability: https://doi.org/10.1093/ejcts/ezaa277; http://academic.oup.com/ejcts/article-pdf/59/1/147/35388763/ezaa277.pdf
Rights: https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model
Accession Number: edsbas.5FC633E4
Database: BASE