Jeon Sea-Yuong, Kim Jin-Pyeong, Kim Eun-Ah, Ahn Seong-Ki, Kim Beom-Gyu
Department of Otolaryngology, Gyeong-Sang National University Hospital, Chinju, Korea.
Ann Otol Rhinol Laryngol. 2005 May;114(5):393-8. doi: 10.1177/000348940511400511.
Platelet-activating factor (PAF) is known to be a potent inflammatory mediator, especially in allergic inflammation. However, the exact role of PAF in the pathogenesis of rhinosinusitis has not been clearly established. To understand the role of PAF in the pathogenesis of rhinosinusitis, it is necessary to develop an animal model of PAF-induced rhinosinusitis. The aim of this study was to develop a rat model of rhinosinusitis induced by intranasally applied PAF. Fifty microliters of 16 microg/mL PAF was applied intranasally through each naris in 4-week-old Sprague-Dawley rats, and the same amount of vehicle was applied in control rats. At 1, 3, or 5 days, the animals were painlessly sacrificed, and the nasal cavity and sinuses were prepared for histologic investigation. The histologic sections were examined in a blind manner for the appearance of neutrophil clusters in the sinonasal air space, and the numbers of eosinophils, areas of epithelial loss, goblet cells, and inducible nitric oxide synthase (iNOS)-positive inflammatory cells in the mucosa. Neutrophil clusters were observed in the air space, and the number of eosinophils, areas of epithelial loss, goblet cells, and iNOS-positive inflammatory cells in the mucosa were increased significantly in the PAF-applied rats. The amount of inflammation varied according to the time interval, showing a peak at day 3. We conclude that intranasally applied PAF induces rhinosinusitis in rats. The histologic evidence of rhinosinusitis revealed the appearance of neutrophil clusters in the sinonasal air space, infiltration of eosinophils and iNOS-positive inflammatory cells in the mucosa, areas of epithelial loss, and goblet cell hyperplasia in the epithelium. This rat model of PAF-induced rhinosinusitis may be applied for better understanding of the role of PAF in the pathogenesis of rhinosinusitis.
血小板活化因子(PAF)是一种强效的炎症介质,尤其在过敏性炎症中。然而,PAF在鼻窦炎发病机制中的确切作用尚未明确。为了解PAF在鼻窦炎发病机制中的作用,有必要建立PAF诱导的鼻窦炎动物模型。本研究的目的是建立经鼻应用PAF诱导的大鼠鼻窦炎模型。将50微升16微克/毫升的PAF经鼻分别注入4周龄的Sprague-Dawley大鼠的每个鼻孔,对照组大鼠注入等量的赋形剂。在第1、3或5天,将动物无痛处死,准备鼻腔和鼻窦进行组织学检查。组织学切片以盲法检查鼻窦气腔内中性粒细胞簇的出现情况,以及黏膜中嗜酸性粒细胞的数量、上皮缺失面积、杯状细胞和诱导型一氧化氮合酶(iNOS)阳性炎症细胞的数量。在PAF处理的大鼠气腔内观察到中性粒细胞簇,黏膜中嗜酸性粒细胞数量、上皮缺失面积、杯状细胞和iNOS阳性炎症细胞数量显著增加。炎症程度随时间间隔而变化,在第3天达到峰值。我们得出结论,经鼻应用PAF可诱导大鼠鼻窦炎。鼻窦炎的组织学证据显示鼻窦气腔内出现中性粒细胞簇,黏膜中有嗜酸性粒细胞和iNOS阳性炎症细胞浸润、上皮缺失区域以及上皮内杯状细胞增生。这种PAF诱导的大鼠鼻窦炎模型可用于更好地理解PAF在鼻窦炎发病机制中的作用。