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Characterization of a murine model of monocrotaline pyrrole-induced acute lung injury
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
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
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.
Keywords:
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