Influence on Nasal Sinuses Mucosa Epithelium GR and IκBα Expression for Chronic Rhinosinusitis Model Treated with Bi-Yuan-Shu Oral Liquid
10.11842/wst.2014.01.018
- VernacularTitle:鼻渊舒口服液对慢性鼻-鼻窦炎模型鼻窦黏膜上皮GR及IκBα表达的影响
- Author:
Hui LI
;
Tianmin ZHU
- Publication Type:Journal Article
- Keywords:
Bi-Yuan-Shu;
chronic rhinosinusitis;
nasal sinuses mucosa epithelium;
glucocorticoid receptors;
IκBα
- From:
World Science and Technology-Modernization of Traditional Chinese Medicine
2014;(1):98-102
- CountryChina
- Language:Chinese
-
Abstract:
This study was aimed to investigate the influence of Bi-Y uan-Shu (BYS) Oral Liquid on glucocorticoid re-ceptor (GR) and nuclear factor IκBα expression of nasal sinuses mucosa epithelium among chronic rhinosinusitis (CRS) models in order to explore its therapeutic mechanism for CRS from the anti-inflammatory reaction aspect. One hundred New Zealand rabbits were selected and randomly divided into the normal group, sham operation group, model group, BYS group, and clarithromycin group, with 20 rabbits in each group. After the CRS model was established, no intervention was given to the normal group, sham operation group, or model group. The intragastric administrations of BYS (1.5 mL·kg-1·d-1) and clarithromycin (25 mg·kg-1·d-1) were given for 14 days, respectively. The nasal sinuses mucosa was taken after the treatment. And HE stain was used to observe its pathological changes. Western Blotting was used in the detection of nasal sinuses mucosal epithelium cytoplasm GR and IκBα expression. The results showed that there were obvious nasal sinuses mucosa inflammatory cell infiltration, chronic inflammation changes, and obvious hyperplasia of glandular organs and goblet cells. Compared with the normal group, the GR expression was obviously reduced (P< 0.01). And the IκBα expression was obviously increased (P< 0.01). After the intragastric administration of BYS, the nasal sinuses mucosal epithelium was repaired with no obvious inflammatory cell infiltration, glandular organs, or goblet cells. Compared with the model group, the GR expression was obviously increased (P< 0.01). The IκBα expression was obviously decreased (P<0.01). It was concluded that BYS can promote GR expression to inhibit inflammation. Meanwhile, it can restrain IκBα expression to prevent the over inhabitation of IκBα on NF-κB. It can dynamically regulate the balance of the nasal sinuses mucosa epithelium inflammation.
