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首页> 外文期刊>Annals of allergy, asthma, and immunology >Induction of airway remodeling of nasal mucosa by repetitive allergen challenge in a murine model of allergic rhinitis.
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Induction of airway remodeling of nasal mucosa by repetitive allergen challenge in a murine model of allergic rhinitis.

机译:在变应性鼻炎的小鼠模型中,通过反复的变应原激发,诱导鼻粘膜的气道重塑。

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BACKGROUND: Although many studies regarding airway remodeling in asthma have been reported, only a few studies have investigated airway remodeling in allergic rhinitis. OBJECTIVES: To determine whether repetitive allergen challenge could induce airway remodeling in the nose and evaluate the effect of steroids using a murine model of allergic rhinitis. METHODS: To develop a mouse model of airway remodeling, ovalbumin-sensitized mice were repeatedly exposed to inhaled ovalbumin administration twice a week for 1 month and 3 months. Matched control mice were challenged with phosphate-buffered saline, and the treatment group received intraperitoneal dexamethasone injection. Trichrome, periodic acid-Schiff, hematoxylin-eosin, and immunohistochemical staining against matrix metalloproteinase 9 and tissue inhibitors of metalloproteinase 1 were performed to nasal and lung tissues, and the level of transforming growth factor beta in the nasal lavage fluid was analyzed. RESULTS: Repetitive ovalbumin challenge for3 months induced circumferential peribronchial fibrosis in the lung. In the nose, subepithelial fibrosis, increased matrix metalloproteinase 9 and tissue inhibitors of metalloproteinase 1 expression, goblet cell hyperplasia, and submucous gland hypertrophy were observed compared with the control group. Features of airway remodeling were more prominent in the lung tissue. Administration of dexamethasone significantly inhibited these histologic changes. CONCLUSION: Airway remodeling associated with long-term allergen challenge can occur in the nasal mucosa and the lung. Steroid treatment prevents airway inflammation in response to acute allergen challenge, as well as airway remodeling by long-term allergen challenge.
机译:背景:尽管已报道了许多有关哮喘气道重塑的研究,但只有少数研究调查了过敏性鼻炎的气道重塑。目的:通过使用鼠源性变应性鼻炎模型,确定重复性变应原刺激是否可引起鼻子气道重塑,并评估类固醇的作用。方法:为建立气道重塑小鼠模型,卵白蛋白致敏小鼠每周两次反复吸入吸入卵白蛋白,持续1个月和3个月。配对的对照小鼠用磷酸盐缓冲盐水攻击,治疗组接受腹膜内地塞米松注射。对鼻和肺组织进行了三色,高碘酸-希夫,苏木精-伊红和基质金属蛋白酶9和金属蛋白酶1组织抑制剂的免疫组化染色,并分析了鼻灌洗液中转化生长因子β的水平。结果:重复卵清蛋白刺激3个月导致肺周支气管周纤维化。与对照组相比,在鼻子中观察到上皮下纤维化,基质金属蛋白酶9升高和金属蛋白酶1表达的组织抑制剂,杯状细胞增生和粘膜下肥大。气道重塑的特征在肺组织中更为突出。地塞米松的给药显着抑制了这些组织学改变。结论:与长期变应原攻击有关的气道重塑可发生在鼻粘膜和肺中。类固醇治疗可预防因急性过敏原激发而引起的气道炎症,以及长期过敏原激发引起的气道重塑。

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