Characterization of a murine model of monocrotaline pyrrole-induced acute lung injury |
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Authors: | Rio Dumitrascu Silke Koebrich Eva Dony Norbert Weissmann Rajkumar Savai Soni S Pullamsetti Hossein A Ghofrani Arun Samidurai Horst Traupe Werner Seeger Friedrich Grimminger Ralph T Schermuly |
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Affiliation: | 1. University of Giessen Lung Center (UGLC), Giessen, Germany 3. Max-Planck-Institute for Heart and Lung Research, Bad Nauheim, Germany 2. Department of Neuroradiology, Justus-Liebig-University of Giessen, Germany
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Abstract: | Background New animal models of chronic pulmonary hypertension in mice are needed. The injection of monocrotaline is an established model of pulmonary hypertension in rats. The aim of this study was to establish a murine model of pulmonary hypertension by injection of the active metabolite, monocrotaline pyrrole. Methods Survival studies, computed tomographic scanning, histology, bronchoalveolar lavage were performed, and arterial blood gases and hemodynamics were measured in animals which received an intravenous injection of different doses of monocrotaline pyrrole. Results Monocrotaline pyrrole induced pulmonary hypertension in Sprague Dawley rats. When injected into mice, monocrotaline pyrrole induced dose-dependant mortality in C57Bl6/N and BALB/c mice (dose range 6–15 mg/kg bodyweight). At a dose of 10 mg/kg bodyweight, mice developed a typical early-phase acute lung injury, characterized by lung edema, neutrophil influx, hypoxemia and reduced lung compliance. In the late phase, monocrotaline pyrrole injection resulted in limited lung fibrosis and no obvious pulmonary hypertension. Conclusion Monocrotaline and monocrotaline pyrrole pneumotoxicity substantially differs between the animal species. |
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