Related Experiment Video
Updated: Mar 23, 2026

Establishment and Validation of a Rat Model of Pulmonary Arterial Hypertension Associated with Pulmonary Fibrosis
Published on: May 23, 2025
Development and Characterization of an Inducible Rat Model of Chronic Thromboembolic Pulmonary Hypertension
Paula-Anahi Arias-Loza1, Pius Jung1, Marco Abeßer1
1From the Department of Internal Medicine I, University Clinic of Wuerzburg, Wuerzburg, Germany (P.-A.A.-L., P.J., S.U., T.W., S.F., T.P.); Comprehensive Heart Failure Center Wuerzburg, Wuerzburg, Germany (P.-A.A.-L., S.U., T.W., T.P.); Institute of Physiology, University Wuerzburg, Wuerzburg, Germany (M.A., K.S.); and University Clinic and Polyclinic for Internal Medicine III, University Clinic Halle, Halle, Germany (S.F.).
Abstract:
Chronic thromboembolic pulmonary hypertension (CTEPH) is an entity of PH that not only limits patients quality of life but also causes significant morbidity and mortality. The treatment of choice is pulmonary endarterectomy. However numerous patients do not qualify for pulmonary endarterectomy or present with residual vasculopathy post pulmonary endarterectomy and require specific vasodilator treatment. Currently, there is no available specific small animal model of CTEPH that could serve as tool to identify targetable molecular pathways and to test new treatment options. Thus, we generated and standardized a rat model that not only resembles functional and histological features of CTEPH but also emulates thrombi fibrosis. The pulmonary embolism protocol consisted of 3 sequential tail vein injections of fibrinogen/collagen-covered polystyrene microspheres combined with thrombin and administered to 10-week-old male Wistar rats. After the third embolism, rats developed characteristic features of CTEPH including elevated right ventricular systolic pressure, right ventricular cardiomyocyte hypertrophy, pulmonary artery remodeling, increased serum brain natriuretic peptide levels, thrombi fibrosis, and formation of pulmonary cellular-fibrotic lesions. The current animal model seems suitable for detailed study of CTEPH pathophysiology and permits preclinical testing of new pharmacological therapies against CTEPH.

