Yan-Hou-Qing formula attenuates allergic airway inflammation via up-regulation of Treg and suppressing Th2 responses in Ovalbumin-induced asthmatic mice

被引:17
作者
Cheng, Bao-Hui [1 ,2 ]
Hu, Tian-Yong [1 ,2 ]
Mo, Li-Hua [1 ,2 ]
Ma, Li [1 ,2 ]
Hu, Wen-Hui [1 ,2 ]
Li, Yi-Sheng [1 ,2 ]
Liu, Zhi-Qiang [1 ,2 ]
Qiu, Shu-Qi [1 ,2 ]
机构
[1] Inst ENT, Shenzhen Key Lab ENT, Shenzhen 518172, Peoples R China
[2] Longgang ENT Hosp, 3004 Longgang Ave, Shenzhen 518172, Peoples R China
基金
中国国家自然科学基金;
关键词
YHQ; Allergic asthma; Treg; Th2; AHR; T-CELLS; PHYTOCHEMISTRY; PHARMACOLOGY; MECHANISMS; RHINITIS; EXTRACT; MODELS;
D O I
10.1016/j.jep.2018.11.038
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Yan-Hou-Qing (YHQ), a Chinese medicine formula containing fourteen kinds of materials, has been designed for pharyngitis and cough treatment in Oriental medicine. In the present study, the anti-allergic effects and underlying mechanisms of YHQ in inhibition of airway hyper responsiveness (AHR) was explored in an ovalbumin (OVA)-induced allergic asthma mouse model. Materials and methods: BALB/c mice were sensitized by OVA and cholera toxin (CT) and challenged with OVA intranasally to induce allergic asthma mouse model. YHQ (200 mg/kg) was orally administered for 3 weeks from week-2 after OVA sensitization. The AHR and histological changes of lung tissues were evaluated by whole-body barometric plethysmography analysis and hematoxylin and eosin (H&E) staining, respectively. The serum concentration of OVA-specific lgE and T helper 2 (Th2) cytokines (IL-4 and IL-13) were determined by enzyme linked immune sorbent assay (ELISA). Flow cytometry was performed to evaluate the percentage of CD4(+)CD25(+)Foxp3(+) regulatory T cells (Treg) in the spleen. Results: The elevated AHR responses, heavier inflammatory cell infiltration and Th2 cytokines in allergic asthma group indicated Ovalbumin-induced asthmatic mouse models were built successfully. Compared to allergic asthma group, OVA-induced AHR responses and eosinophil infiltration in lung were improved significantly, and the productions of OVA-specific IgE and Th2 cytokines, IL-4 and IL-13, in the serum were also reduced dramatically after the treatment of YHQ. Moreover, YHQ treatment significantly increased the percentage of CD4(+)CD25(+)Foxp3(+) Treg in OVA-induced allergic asthma mouse model. Conclusions: YHQ improves the allergic asthma related symptoms via promotion of CD4(+)CD25(+) Foxp3(+) Treg and suppression of Th2 responses in mouse model, suggesting YHQ can be used as a potent agent to alleviate allergic asthma related symptoms.
引用
收藏
页码:275 / 282
页数:8
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