Abstract | RATIONALE: METHODS: Adult male Wistar rats were randomly assigned to the following groups: untreated animals (controls), Bleomycin-induced PF ( Bleomycin) and Bleomycin-induced PF treated with Bosentan (Bleomycin+Bosentan). Exercise capacity was evaluated by treadmill exercise testing. PH was assessed by right ventricular systolic pressure (RVSP) and right ventricular hypertrophy. For quantification of PF the hydroxyproline content in lung tissue (HPC) was measured. RESULTS: Compared to controls, animals with Bleomycin-induced PF showed a significant reduction in exercise capacity (44% vs. 100%), significantly higher RVSP (65 mmHg vs. 23 mmHg), significantly more right ventricular hypertrophy (0.55 vs. 0.24) and significantly higher HPC (60.5 vs. 14.8). Bosentan treatment in animals with Bleomycin-induced PF resulted in significantly greater exercise capacity (98% vs. 44%) and a trend towards lower RVSP (52 mmHg vs. 65 mmHg), significantly less right ventricular hypertrophy (0.34 vs. 0.55) and significantly lower HPC (16.7 vs. 60.5) compared to untreated Bleomycin-induced PF. CONCLUSION: Application of Bosentan in Bleomycin rats resulted in significantly higher exercise capacity as a result of improvements in PH and PF.
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Authors | Stephan Schroll, Michael Arzt, Daniela Sebah, Martin Nüchterlein, Friedrich Blumberg, Michael Pfeifer |
Journal | Respiratory physiology & neurobiology
(Respir Physiol Neurobiol)
Vol. 170
Issue 1
Pg. 32-6
(Jan 31 2010)
ISSN: 1878-1519 [Electronic] Netherlands |
PMID | 19931426
(Publication Type: Journal Article)
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Copyright | Copyright 2009 Elsevier B.V. All rights reserved. |
Chemical References |
- Antibiotics, Antineoplastic
- Antihypertensive Agents
- CCN2 protein, rat
- Sulfonamides
- Bleomycin
- Connective Tissue Growth Factor
- Collagen
- Bosentan
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Topics |
- Analysis of Variance
- Animals
- Antibiotics, Antineoplastic
(adverse effects)
- Antihypertensive Agents
(therapeutic use)
- Bleomycin
(adverse effects)
- Bosentan
- Collagen
(metabolism)
- Connective Tissue Growth Factor
(genetics, metabolism)
- Disease Models, Animal
- Hemodynamics
(drug effects)
- Hypertension, Pulmonary
(chemically induced, drug therapy)
- Hypertrophy, Right Ventricular
(drug therapy, pathology)
- Lung
(drug effects, metabolism)
- Male
- Physical Conditioning, Animal
(physiology)
- Pulmonary Fibrosis
(chemically induced, drug therapy)
- Rats
- Rats, Wistar
- Sulfonamides
(therapeutic use)
- Time Factors
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