Effects of (±)-praeruptorin A on airway inflammation, airway hyperresponsiveness and NF-κB signaling pathway in a mouse model of allergic airway disease

被引:43
作者
Xiong, Youyi [1 ]
Wang, Junsong [1 ]
Wu, Feihua [2 ]
Li, Juan [2 ]
Zhou, Linfu [3 ]
Kong, Lingyi [1 ]
机构
[1] China Pharmaceut Univ, Dept Nat Med Chem, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Dept Pharmacol Chinese Mat Med, Nanjing 211198, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Resp Med, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Praeruptorin A; Airway inflammation; Asthma; Allergic diseases; Peucedanum praeruptorum Dunn; TRANSCRIPTION FACTOR; QIAN-HU; ASTHMA; PRAERUPTORIN; EXPRESSION; KINASES; TARGET; CELLS;
D O I
10.1016/j.ejphar.2012.03.004
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The root of Peucedanum praeruptorum Dunn is a traditional Chinese medicine commonly used to treat asthma in China. (+/-)-praeruptorin A (PA) is the most abundant constituent of P. praeruptorum Dunn, the effects of which on asthma were investigated using a murine model of allergic airway disease. BALB/c mice were sensitized and challenged by ovalbumin to induce airway inflammation. PA was administered intragastrically before every OVA challenge. Airway responsiveness was measured by a lung function analysis system. The number of total leukocytes in bronchoalveolar lavage fluid was counted using a hemocytometer, and differential cell counts were determined using Diff-Quick-stained smears. Histopathology of lung tissue was analyzed by hematoxylin-eosin and Congo red staining. Levels of inflammatory mediators in bronchoalveolar lavage fluid and immunoglobulins in serum were measured by enzyme-linked immunosorbent assay. The expression of pulmonary eotaxin was detected by immunohistochemistry and reverse transcription polymerase chain reaction. The activation of NF-kappa B was evaluated by electrophoretic mobility shift assay and western blot analysis. Compared with model group, PA significantly reduced airway hyperresponsiveness and airway eosinophilic inflammation, improved pathologic lesion of the lungs, reduced levels of interleukin (IL)-4, IL-5, IL-13 and LTC4 in bronchoalveolar lavage fluid and immunoglobulin (Ig) E in serum, and inhibited eotaxin protein and mRNA expression, I kappa B alpha degradation, NF-kappa B nuclear translocation, NF-kappa B DNA-binding activity and RelA/p65 phosphorylation in lung, which suggested that PA can significantly suppress OVA-induced airway inflammation and airway hyperresponsiveness in mice, showing great therapeutic potential for the treatment of allergic asthma. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:316 / 324
页数:9
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