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变应原诱导的鼻气道重塑大鼠模型的时间进程研究。

A time course study on the development of allergen-induced nasal airway remodeling in a rat model.

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Dankook University College of Medicine, Cheonan, Korea.

出版信息

Am J Rhinol Allergy. 2012 Nov-Dec;26(6):421-7. doi: 10.2500/ajra.2012.26.3823.

DOI:10.2500/ajra.2012.26.3823
PMID:23232190
Abstract

BACKGROUND

Only a few studies have investigated the airway remodeling process in allergic rhinitis (AR), and the results reported are conflicting. We established an allergen-induced nasal remodeling model for AR using brown Norway rats and investigated time-dependent histological changes and the reversibility of the epithelial and subepithelial changes.

METHODS

Ovalbumin (OVA)-sensitized rats were exposed to OVA daily and then assigned to one of five groups depending on the duration of the challenge. Groups I, II, III, and IV rats were exposed for 1, 4, 8, and 12 weeks, respectively. Group V rats were exposed for 12 weeks and then protected from challenge for 4 weeks. Matched control rats were exposed to saline. Histological parameters of the nasal mucosa such as epithelial and subepithelial thickness, goblet cell hyperplasia, eosinophil infiltration, submucosal gland hypertrophy, and expression of matrix metalloproteinase-9 (MMP-9) and tissue inhibitor of metalloproteinase-1 (TIMP-1) were compared between groups.

RESULTS

Repeated challenges for 12 weeks resulted in the characteristic features of nasal airway remodeling. All parameters except epithelial thickness increased markedly. Goblet cell hyperplasia and eosinophil infiltration decreased to control group levels after cessation of challenge for 4 weeks. Subepithelial changes such as subepithelial thickening, submucosal gland hypertrophy, and increased expression of MMP-9 and TIMP-1 were still observed after 4 weeks without challenge.

CONCLUSION

Our results indicate that prolonged OVA challenge can induce nasal remodeling. Epithelial changes were minimal or absent after cessation of the challenge, but subepithelial changes were resistant to reversal.

摘要

背景

仅有少数研究调查了变应性鼻炎(AR)的气道重塑过程,且报告的结果相互矛盾。我们使用褐家鼠建立了变应原诱导的 AR 鼻重塑模型,并研究了时间依赖性组织学变化以及上皮和上皮下变化的可逆性。

方法

卵清蛋白(OVA)致敏大鼠每日接受 OVA 暴露,然后根据暴露时间长短分为五组。第 I、II、III 和 IV 组大鼠分别暴露 1、4、8 和 12 周,第 V 组大鼠暴露 12 周后保护免于暴露 4 周。匹配的对照大鼠暴露于生理盐水。比较各组鼻黏膜的组织学参数,如上皮和上皮下厚度、杯状细胞增生、嗜酸性粒细胞浸润、黏膜下腺肥大以及基质金属蛋白酶-9(MMP-9)和金属蛋白酶组织抑制剂-1(TIMP-1)的表达。

结果

反复 12 周的挑战导致了鼻气道重塑的特征性变化。除上皮厚度外,所有参数均显著增加。停止暴露 4 周后,杯状细胞增生和嗜酸性粒细胞浸润下降至对照组水平。停止暴露 4 周后,仍观察到上皮下变化,如上皮下增厚、黏膜下腺肥大以及 MMP-9 和 TIMP-1 表达增加。

结论

我们的结果表明,长时间的 OVA 暴露可诱导鼻重塑。停止暴露后上皮变化很小或不存在,但上皮下变化仍难以逆转。

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