Wakahara Keiko, Tanaka Hiroyuki, Takahashi Go, Tamari Mayumi, Nasu Reishi, Toyohara Tatsuyuki, Takano Hirohisa, Saito Saburo, Inagaki Naoki, Shimokata Kaoru, Nagai Hiroichi
Department of Pharmacology, Gifu Pharmaceutical University, Gifu, Japan.
Eur J Pharmacol. 2008 Jan 6;578(1):87-96. doi: 10.1016/j.ejphar.2007.09.005. Epub 2007 Sep 20.
Dermatophagoides farinae are known to be a common environmental allergen causing allergic asthma; however, little is known about their pathophysiological effect via the allergenicities in vivo. Therefore, we first established a mouse model of asthma induced by repeated instillations of D. farinae. Second, to investigate whether the asthmatic responses are Th2-dependent, we examined the effect of the deficiency of interleukin-4 (IL-4) receptor alpha chain gene. Finally, we examined the effect of fluticasone propionate on this model. Mice were instilled with D. farinae without additional adjuvants into the trachea 8 times. After the final allergen instillation, the airway responsiveness to acetylcholine was measured, and bronchoalveolar lavage and histological examination were carried out. The instillation of the allergen-induced airway hyperresponsiveness, the accumulation of inflammatory cells and increases in the levels of Th2 cytokines and transforming growth factor-beta(1) production in the bronchoalveolar lavage fluid dose dependently. The number of goblet cells in the epithelium and the extent of the fibrotic area beneath the basement membrane were also increased in the morphometric study. In contrast, the defect of IL-4/IL-13 signaling through IL-4 receptor alpha chain completely abrogated all these responses. Furthermore, the simultaneous instillation of fluticasone propionate with the allergen showed significant inhibition or an inhibitory tendency of these changes. These findings demonstrate that the repetitive intratracheal instillations of D. farinae can induce airway remodeling through Th2-type inflammation, and that fluticasone propionate inhibits D. farinae-induced airway remodeling in mice, and this model would be useful for studying mechanisms involved in the development of allergic asthma.
已知粉尘螨是引起过敏性哮喘的常见环境过敏原;然而,关于它们通过体内过敏原性产生的病理生理效应却知之甚少。因此,我们首先建立了通过反复滴注粉尘螨诱导的小鼠哮喘模型。其次,为了研究哮喘反应是否依赖于Th2,我们检测了白细胞介素-4(IL-4)受体α链基因缺陷的影响。最后,我们检测了丙酸氟替卡松对该模型的影响。将粉尘螨在无额外佐剂的情况下经气管滴注到小鼠体内8次。在最后一次过敏原滴注后,测量气道对乙酰胆碱的反应性,并进行支气管肺泡灌洗和组织学检查。过敏原的滴注剂量依赖性地诱导气道高反应性、炎症细胞积聚以及支气管肺泡灌洗液中Th2细胞因子水平升高和转化生长因子-β(1)产生增加。形态学研究还显示上皮中杯状细胞数量和基底膜下纤维化区域范围增加。相反,通过IL-4受体α链的IL-4/IL-13信号缺陷完全消除了所有这些反应。此外,丙酸氟替卡松与过敏原同时滴注显示出对这些变化的显著抑制或抑制趋势。这些发现表明,反复经气管滴注粉尘螨可通过Th2型炎症诱导气道重塑,并且丙酸氟替卡松可抑制粉尘螨诱导的小鼠气道重塑,该模型将有助于研究过敏性哮喘发生发展的相关机制。