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首页> 外文期刊>International immunopharmacology >Comparison of the efficacy of KOB03, ketotifen, and montelukast in an experimental mouse model of allergic rhinitis
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Comparison of the efficacy of KOB03, ketotifen, and montelukast in an experimental mouse model of allergic rhinitis

机译:比较KOB03,酮替芬和孟鲁司特在变应性鼻炎实验小鼠模型中的功效

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KOB03 is a polyherbal medicine derived from an oriental prescription traditionally used to treat allergic diseases. In the present study, we compared the efficacy of KOB03 with modern drugs such as ketotifen and montelukast in an experimental mouse model of allergic rhinitis (AR). Ketotifen is a H1 receptor antagonist and montelukast is a leukotriene receptor antagonist. Mice were treated with KOB03, ketotifen or montelukast in an established AR mouse model using ovalbumin (OVA)-sensitized/challenged BALB/c mice. The treatment of KOB03 had inhibitory effects on symptom scores, serum levels of OVA-specific IgE, histamine, leukotriene C4, IL-4, TNF-α, and IL-1β in AR mice, and the histolopathological changes of nasal mucosa with mucin release and inflammation. AR mice treated with KOB03 had significantly lower serum levels of OVA-specific IgE, LTC4, IL-4, and IL-1β than mice treated with ketotifen, whereas they only had significantly lower serum levels of OVA-specific IgE and IL-4 than those treated with montelukast. In addition, the histolopathological changes of nasal mucosa with eosinophil infiltration were significantly lower in the KOB03-treated mice than those in the ketotifen and montelukast-treated group. These results suggest that KOB03 has therapeutic potential for treating AR like other modern medicines.
机译:KOB03是一种多草药,源自传统上用于治疗过敏性疾病的东方处方。在本研究中,我们在过敏性鼻炎(AR)的实验小鼠模型中比较了KOB03与现代药物(例如酮替芬和孟鲁司特)的疗效。酮替芬是H1受体拮抗剂,孟鲁司特是白三烯受体拮抗剂。在已建立的AR小鼠模型中,使用卵清蛋白(OVA)致敏/挑战性BALB / c小鼠,用KOB03,ketotifen或montelukast治疗小鼠。 KOB03的治疗对AR小鼠的症状评分,OVA特异性IgE,组胺,白三烯C4,IL-4,TNF-α和IL-1β的血清水平以及鼻粘膜释放粘蛋白的组织病理学变化具有抑制作用和炎症。与用酮替芬治疗的小鼠相比,用KOB03治疗的AR小鼠的血清OVA特异性IgE,LTC4,IL-4和IL-1β显着降低,而它们的血清OVA特异性IgE和IL-4却显着低于那些接受孟鲁司特治疗的患者。另外,KOB03治疗的小鼠鼻黏膜组织嗜酸性粒细胞浸润的组织病理学变化明显低于酮替芬和孟鲁司特治疗组。这些结果表明,KOB03具有像其他现代药物一样的治疗AR的治疗潜力。

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