Genetics and Molecular Research · 2014 · 17 citations · 12 references
Acute Lung InjuryInflammatory Lung DiseaseLung InflammationPathologyRat ModelsEphedra Sinica StapfInflammation6-Keto-prostaglandin F1αPulmonary PharmacologyFibrosisVascular PharmacologyPulmonary FibrosisVascular BiologyPharmacologyComparative StudyPulmonary DiseasePulmonary Vascular DiseaseAnti-inflammatoryPhysiologyEndothelial DysfunctionCombination TherapyMedicine
The aim of this study was to evaluate differences in the effects of Ephedra sinica Stapf and Fructus Schisandrae Chinensis on angiogenesis in the treatment of bleomycin-induced rat idiopathic pulmonary fibrosis. The rat models were created using bleomycin. The animals were divided into six groups: model, control, Ephedra alone, Schisandrae alone, combination of Ephedra and Schisandrae, and hydrocortisone alone. The treatments were administered for 28 days. After 7 and 28 days, the rats were sacrificed for pathological morphology examination, microvascular density determination, and angiogenesis-related cytokine examination. The Ephedra and hydrocortisone groups demonstrated significantly reduced alveolitis and pulmonary fibrosis grades compared with the model group (P < 0.05). The number of blood vessels in the Ephedra group was higher than that in the Schisandrae and combination therapy groups. At 7 days, the expression level of endothelin (ET)-1 in the model group was significantly higher than that in the normal group (P < 0.01). The level of 6-keto-prostaglandin F1α (6-keto-PGF1α) in the treatment group increased, and there were significant differences between the Ephedra group and the combination therapy and normal groups (P < 0.05). Ephedra inhibited the increase in the lung coefficient. The combination therapy prevented pulmonary artery injury and angiogenesis of the arteries by reducing the level of ET-1 and promoting the level of 6-keto-PGF1α in the blood. Ephedra and Schisandrae prevented alveolitis and the development of pulmonary fibrosis.
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Bleomycin-induced interstitial pulmonary disease in the nude, athymic mouse.
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Inflammatory Lung Disease, Lung Inflammation, Immunology +17
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