Prevention of allergic airway hyperresponsiveness and remodeling in mice by Astragaliradix Antiasthmatic decoction

被引:15
作者
Xu, Su [1 ]
Tian, Bao-Ping [1 ]
Zhang, Lan-Hong [1 ]
Hua, Wen [1 ]
Xia, Li-Xia [1 ]
Chen, Zhi-Hua [1 ]
Li, Wen [1 ]
Shen, Hua-Hao [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Resp & Crit Care Med, Affiliated Hosp 2, Sch Med, Hangzhou 310009, Zhejiang, Peoples R China
[2] State Key Lab Resp Dis, Guangzhou 510120, Guangdong, Peoples R China
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2013年 / 13卷
基金
中国国家自然科学基金;
关键词
Astragalus Antiasthmatic Decoction; Airway hyperresponsiveness; Airway remodeling; INTERFERON-GAMMA; ASTHMA; CODONOPSIS; CHINENSIS; CELLS; BETA;
D O I
10.1186/1472-6882-13-369
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Astragali radix Antiasthmatic Decoction (AAD), a traditional Chinese medication, is found effective in treating allergic diseases and chronic cough. The purpose of this study is to determine whether this medication could suppress allergen-induced airway hyperresponsiveness (AHR) and remodeling in mice, and its possible mechanisms. Methods: A mouse model of chronic asthma was used to investigate the effects of AAD on the airway lesions. Mice were sensitized and challenged with ovalbumin (OVA), and the extent of AHR and airway remodeling were characterized. Cells and cytokines in the bronchoalveolar lavage fluid (BALF) were examined. Results: AAD treatment effectively decreased OVA-induced AHR, eosinophilic airway inflammation, and collagen deposition around the airway. It significantly reduced the levels of IL-13 and TGF-beta 1, but exerted inconsiderable effect on INF-gamma and IL-10. Conclusions: AAD greatly improves the symptoms of allergic airway remodeling probably through inhibition of Th2 cytokines and TGF-beta 1.
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页数:8
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