Feitai attenuates bleomycin-induced pulmonary fibrosis in rats
Gong, LK; Li, XH; Wang, H; Zhang, L; Cai, Y; Qi, XM; Liu, LL; Liu, YZ; Wu, XF; Chen, FP
刊名BIOLOGICAL & PHARMACEUTICAL BULLETIN
2004-05
卷号27期号:5页码:634-640
关键词Feitai pulmonary fibrosis bleomycin rat
ISSN号0918-6158
DOI10.1248/bpb.27.634
文献子类Article
英文摘要Pulmonary fibrosis is a common consequence of numerous pulmonary diseases. The current therapeutic approaches for this condition are unsatisfactory. Feitai, a composite formula consisting of several herbs, is used in China as a folk remedy for treating patients with pulmonary tuberculosis. In this study, we extensively investigate the effects and mechanisms of Feitai on bleomycin (BLM)-induced pulmonary fibrosis in rats. One hundred and twenty male Sprague-Dawley rats were randomly divided into four groups, referred to as the saline-water, saline-Feitai, BLM-water, and BLM-Feitai groups. Following a single instillation of BLM (5 mg/kg) or saline, rats were orally administered Feitai at a dose of 3 g/kg body weight or sterilized distilled water once daily. Rats were killed at 7, 14, or 28 d post-BLM. Inflammatory cell count, protein concentration, and lactate dehydrogenase activity in bronchoalveolar lavage fluid were measured, and myeloperoxidase activity and lipid peroxide content in lung homogenates were analyzed. Treatment with Feitai inhibited lung fibrotic progression induced by BLM, as indicated by the decrease in lung hydroproline content and lung fibrosis score at 28 d post-BLM. This was accompanied by significant amelioration of BLM-induced body weight loss, lung edema, and inflammatory response during the development of lung injury in the acute phase. The results strongly indicate the beneficial effects of Feitai in protecting against BLM-induced pulmonary fibrosis. Furthermore, the inflammatory response and lipid peroxidation were inhibited by Feitai, suggesting that the effect of this formula on BLM-induced lung injury and fibrosis is associated with antiinflammatory and antioxidant properties.
WOS关键词INDUCED LUNG FIBROSIS ; N-ACETYLCYSTEINE ; GROWTH-FACTOR ; MICE ; INJURY ; PATHOGENESIS ; SUPEROXIDE ; SURFACTANT ; TOXICITY ; DAMAGE
WOS研究方向Pharmacology & Pharmacy
语种英语
出版者PHARMACEUTICAL SOC JAPAN
WOS记录号WOS:000221161200008
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/274082]  
专题药物安全性评价中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Ren, J
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai Inst Biol Sci, Shanghai 201203, Peoples R China
2.Shanghai Pulm Hosp, Shanghai 200043, Peoples R China
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GB/T 7714
Gong, LK,Li, XH,Wang, H,et al. Feitai attenuates bleomycin-induced pulmonary fibrosis in rats[J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN,2004,27(5):634-640.
APA Gong, LK.,Li, XH.,Wang, H.,Zhang, L.,Cai, Y.,...&Ren, J.(2004).Feitai attenuates bleomycin-induced pulmonary fibrosis in rats.BIOLOGICAL & PHARMACEUTICAL BULLETIN,27(5),634-640.
MLA Gong, LK,et al."Feitai attenuates bleomycin-induced pulmonary fibrosis in rats".BIOLOGICAL & PHARMACEUTICAL BULLETIN 27.5(2004):634-640.
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