Chen Zu-Yao, Zhou Shou-Hong, Zhou Qiao-Feng, Tang Hong-Bo
Department of Otorhinolaryngology, The First Affiliated Hospital, University of South China, Hengyang, Hunan 421001, P.R. China.
Institute of Neuroscience, School of Medicine, The First Affiliated Hospital, University of South China, Hengyang, Hunan 421001, P.R. China.
Exp Ther Med. 2017 Oct;14(4):3485-3490. doi: 10.3892/etm.2017.4937. Epub 2017 Aug 16.
Allergic rhinitis (AR) and asthma belong to the category of type I allergic diseases, whose pathological features are airway remodeling of the lung and allergic inflammation. The aim of the present study was to evaluate inflammation and remodeling of lung tissue in a guinea pig model of AR in order to confirm consistent pathological changes of upper and lower airways in AR. Male guinea pigs were randomly divided into an experimental and a control group (n=10 in each). The AR model was established by sensitization through intraperitoneal injection of ovalbumin for three weeks and bilateral nasal local excitation for twelve weeks. All tissues of nasal mucosa and lung were subjected to hematoxylin and eosin as well as toluidine blue staining, and characteristics of remodeling of lung tissue, including thickness of bronchial wall, epithelial mucosa and smooth muscle were histologically determined. Collagen deposition in lung tissue was observed by Masson's trichrome stain. Severe paroxysmal nose scratching action, frequent sneezing, visible outflow of secretion from the anterior naris and frequent nose friction were observed in the AR model group within 30 min after local excitation. The total symptom scores were significantly increased in the AR model group compared with those in the control group. Obvious inflammatory cell infiltration was observed in the AR model group. Compared with those in the control group, the numbers of eosinophils and mast cells in nasal mucosa and lung tissue were significantly increased. Obvious airway remodeling of the lung was observed in the AR model group. Compared with those in the control group, bronchial wall thickness, epithelial layer thickness and smooth muscle thickness in the airways were significantly increased in the AR model group. Increased collagen deposition was found in the AR model group compared with that in the control group. The results of the present study revealed that inflammation and airway remodeling of lungs arose in guinea pigs with AR, suggesting that pathological changes of upper and lower airways are consistent in this AR model.
变应性鼻炎(AR)和哮喘属于Ⅰ型变态反应性疾病范畴,其病理特征为肺部气道重塑和变应性炎症。本研究旨在评估AR豚鼠模型中肺组织的炎症和重塑情况,以证实AR上下气道病理变化的一致性。雄性豚鼠随机分为实验组和对照组(每组n = 10)。通过腹腔注射卵清蛋白致敏3周并双侧鼻腔局部激发12周建立AR模型。对所有鼻黏膜和肺组织进行苏木精-伊红染色以及甲苯胺蓝染色,并组织学测定肺组织重塑特征,包括支气管壁、上皮黏膜和平滑肌厚度。采用Masson三色染色观察肺组织中的胶原沉积。在局部激发后30分钟内,AR模型组观察到严重的阵发性鼻搔抓动作、频繁打喷嚏、前鼻孔可见分泌物流出以及频繁的鼻摩擦。与对照组相比,AR模型组的总症状评分显著增加。AR模型组观察到明显的炎症细胞浸润。与对照组相比,鼻黏膜和肺组织中嗜酸性粒细胞和肥大细胞数量显著增加。AR模型组观察到明显的肺部气道重塑。与对照组相比,AR模型组气道的支气管壁厚度、上皮层厚度和平滑肌厚度显著增加。与对照组相比,AR模型组胶原沉积增加。本研究结果显示,AR豚鼠出现肺部炎症和气道重塑,提示该AR模型中上下气道的病理变化是一致的。