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首页> 外文期刊>Respiration: International Review of Thoracic Diseases >Effects of Zileuton on Airway Smooth Muscle Remodeling after Repeated Allergen Challenge in Brown Norway Rats
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Effects of Zileuton on Airway Smooth Muscle Remodeling after Repeated Allergen Challenge in Brown Norway Rats

机译:齐留通对反复变应原激发的挪威棕色大鼠气道平滑肌重塑的影响

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Background: Chronic asthma is characterized by airway inflammation and remodeling. Objective:This study aimed to evaluate the effects of zileuton on bronchial hyperrespon-siveness, airway inflammation and airway smooth muscle (ASM) remodeling. Methods: Two experimental groups of brown Norway rats sensitized and repeatedly challenged with aerosolized ovalbumin (OA) were given oral zileuton (OA-zileuton group) and oral saline only (OA-saline group). A third, control group was sensitized and challenged by saline. The rats were anesthetized and paralyzed. Pulmonary function tests were performed at baseline and after varying doses of acetylcholine. Bronchoalveolar lavage fluid and lung tissues were examined. Results: Zileuton had beneficial effects on pulmonary function, airway inflammation and ASM remodeling in the OA-zileuton group compared to the OA-saline group. Zileuton inhibited an OA-stimulated increase in ASM by inhibiting hypertrophy, hyperplasia and increased extracellular matrix via the phosphatidylinositol 3-kinase (PI3K)/Akt pathway, thereby reducing cyclin D1 expression and attenuating bronchial hyperresponsiveness. Conclusion: OA increases airway inflammation and ASM mass. Zileuton effectively prevents bronchial hyperresponsiveness, airway inflammation and ASM remodeling in sensitized rats through the PI3K/Akt pathway, which reduces cyclin D1 expression.
机译:背景:慢性哮喘的特征是气道炎症和重塑。目的:本研究旨在评估齐留通对支气管高反应性,气道炎症和气道平滑肌(ASM)重塑的影响。方法:对两个实验组的棕色挪威大鼠进行雾化卵清蛋白(OA)增敏和反复攻击试验,分别给予口服齐留通(OA-zileuton组)和口服生理盐水(OA-盐水组)。第三,对照组致敏并用盐水攻击。将大鼠麻醉并瘫痪。在基线和不同剂量的乙酰胆碱后进行肺功能测试。检查支气管肺泡灌洗液和肺组织。结果:与OA盐水组相比,OA zileuton组对Zileuton的肺部功能,气道炎症和ASM重塑具有有益作用。 Zileuton通过通过磷脂酰肌醇3-激酶(PI3K)/ Akt途径抑制肥大,增生和增加的细胞外基质来抑制OA刺激的ASM升高,从而降低细胞周期蛋白D1的表达并减轻支气管高反应性。结论:OA增加气道炎症和ASM质量。 Zileuton通过PI3K / Akt途径有效防止致敏大鼠的支气管高反应性,气道炎症和ASM重塑,从而降低细胞周期蛋白D1的表达。

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