英文摘要 |
Asthma is a chronic respiratory inflammatory disease that is common public health problem in the world. To date, long-term administration of steroid has been developed for the treatment of asthma although their use is limited by numerous adverse side effects. Magnoliae flos is used in traditional Chinese medicine for treatment of various allergic diseases, including nasal congestion, sinusitis, and allergic rhinitis. Previous study demonstrated magnoliae flos attenuates immediate-type allergic reactions by inhibition of mast cell degranulation both in vivo and in vitro. However, its effect in experiment asthmatic models remains to be investigated. In this study, we evaluated the anti-asthmatic effects of magnoliae flos in ovalbumin (OVA)-sensitized Brown Norway (BN) rats. To accomplish this objective, we used male adult BN rats sensitized with OVA and matching control animals (receiving saline vehicle). Furthermore, the OVA-sensitized rats were randomized into three groups and treated with 3 g/kg magnoliae flos, 10 g/kg magnoliae flos, and vehicle by oral administration for 5 consecutive days. To evaluate airway hyperresponsiveness (e.g. total lung resistance and dynamic lung compliance) to bolus intravenous injection of methacholine (3, 10, 30 μg/kg) were measured in each animal. In addition, to examine airway inflammation, the levels of various inflammatory cells in bronchoalveolar lavage fluid (BALF), serum IgE, and levels of cytokine (e.g. IL-6 and IL-13) in BALF were assessed. Our data showed that OVA sensitization induced airway hyperresponsiveness and infiltration of inflammatory cells (e.g. eosinophil, neutrophil, basophil, lymphocyte, macrophage) in rats. In contrast, OVA sensitization did not significantly increase the levels of IL-6 and IL-13 in BALF and serum IgE. Oral administration of magnoliae flos dose-dependently decreased airway hyperresponsiveness as well as infiltration of eosinophil and lymphocyte in OVA-sensitized rats. Taken together, these data indicated that magnoliae flos may have potential therapeutic value on an OVA-sensitized animal model of allergic asthma. |