Madecassoside Ameliorates Bleomycin-Induced Pulmonary Fibrosis in Mice by Downregulating Collagen Deposition
Autor: | Yue Dai, Jiao-Mei Guo, Zhifeng Wei, Guo-xun Lu, Yu Ji, Si-de Jiang, Yufeng Xia, Difei Bian |
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Rok vydání: | 2014 |
Předmět: |
Pharmacology
Pathology medicine.medical_specialty animal structures medicine.diagnostic_test Inflammation Tissue inhibitor of metalloproteinase Matrix metalloproteinase medicine.disease Bleomycin medicine.disease_cause Malondialdehyde chemistry.chemical_compound Bronchoalveolar lavage chemistry Pulmonary fibrosis medicine medicine.symptom Oxidative stress |
Zdroj: | Phytotherapy Research. 28:1224-1231 |
ISSN: | 0951-418X |
Popis: | This study aimed to explore the protective effects of madecassoside (Mad), a triterpenoid saponin isolated from Centella asiatica herbs, on experimental pulmonary fibrosis (PF) and underlying mechanisms. PF model was established in mice by endotracheal instillation with bleomycin (5 mg/kg). Mice were orally administered with Mad (10, 20, 40 mg/kg) and prednisone (5 mg/kg) for 7 or 21 days. Mad (20, 40 mg/kg) significantly improved lung pathological changes and reduced collagen deposition. In the aspect of collagen synthesis, Mad (20, 40 mg/kg) reduced the expressions of α-smooth muscle actin and transforming growth factor-β1 (TGF-β1), and inhibited the phosphorylations of Smad2 and Smad3 in the lung tissues. However, in vitro, Mad showed little effect on TGF-β1-induced phosphorylation of either Smad2 or Smad3 in primary mouse lung fibroblasts. Moreover, Mad (20, 40 mg/kg) attenuated oxidative damage and inflammation presented at the early stage of PF, evidenced by reduced total leukocytes in the bronchoalveolar lavage fluid, decreased myeloperoxidase activity and malondialdehyde level, and increased super-oxide dismutase activity and glutathione level in lung tissues. On the other hand, Mad (40 mg/kg) elevated the matrix metalloproteinase 1/tissue inhibitor of metalloproteinase 1 ratio in lung tissues of PF mice mainly by downregulating tissue inhibitor of metalloproteinase 1 expression. The present study demonstrated that Mad can ameliorate PF by preventing the deposition of extracellular matrix, which might be achieved mainly through attenuating inflammation and oxidative stress and consequent TGF-β1 overexpression. Copyright © 2014 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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