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雾化吸入对哮喘小鼠模型气道炎症的影响

Effects of Aerosol Inhalation on Airway Inflammation in Asthma Mouse Model.

作者信息

Xiao Huan, Zhang Qian-Nan, Sun Qi-Xiang, Li Lao-Dong, Xu Si-Yue, Li Chao-Qian

机构信息

Department of Emergency and The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Department of Respiratory Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

J Aerosol Med Pulm Drug Deliv. 2021 Dec;34(6):374-382. doi: 10.1089/jamp.2021.0008. Epub 2021 May 4.

Abstract

vaccine, a composition of proteins, has been known to have bidirectional immunomodulatory functions. Recent studies have shown that has a therapeutic potential for treating asthma. However, little is known regarding the effect of aerosol inhalation during allergen sensitization or challenge on asthma. The purpose of this study was to explore the effect and the underlying mechanism of aerosol inhalation during allergen sensitization or challenge on airway inflammation in an asthma mouse model. Asthma mouse models were established. Mice received aerosol inhalation with once daily during allergen sensitization or challenge for 5 days successively. Airway responsiveness, bronchoalveolar lavage fluid (BALF) cell count, histology, and cytokine concentrations (IL-4, IFN-γ, IL-10, and IL-17) were measured. The relative mRNA expression of ASC, caspase-1, TNF-α, and IL-1β was also determined. Expression of pulmonary NLRP3 and nuclear factor kappa B (NF-κB) protein was measured using immunohistochemistry and Western blot. aerosol inhalation suppressed airway hyperresponsiveness and inflammation, reduced levels of IL-4, upregulated expression of IFN-γ and IL-10 in BALF, inhibited mRNA expression of pulmonary ASC, caspase-1, TNF-α, and IL-1β, and also inhibited expression of pulmonary NLRP3 and NF-κB protein during allergen sensitization or challenge. aerosol inhalation can suppress airway hyperresponsiveness and inflammation during allergen sensitization or challenge, and may be a promising approach for asthma therapy.

摘要

疫苗是一种蛋白质组合物,已知具有双向免疫调节功能。最近的研究表明,它对治疗哮喘具有治疗潜力。然而,关于在过敏原致敏或激发期间进行气雾剂吸入对哮喘的影响知之甚少。本研究的目的是探讨在哮喘小鼠模型中,在过敏原致敏或激发期间进行气雾剂吸入对气道炎症的影响及其潜在机制。建立哮喘小鼠模型。在过敏原致敏或激发期间,小鼠连续5天每天接受一次气雾剂吸入。测量气道反应性、支气管肺泡灌洗液(BALF)细胞计数、组织学和细胞因子浓度(IL-4、IFN-γ、IL-10和IL-17)。还测定了ASC、caspase-1、TNF-α和IL-1β的相对mRNA表达。使用免疫组织化学和蛋白质印迹法测量肺NLRP3和核因子κB(NF-κB)蛋白的表达。在过敏原致敏或激发期间,气雾剂吸入可抑制气道高反应性和炎症,降低IL-4水平,上调BALF中IFN-γ和IL-10的表达,抑制肺ASC、caspase-1、TNF-α和IL-1β的mRNA表达,还抑制肺NLRP3和NF-κB蛋白的表达。气雾剂吸入可在过敏原致敏或激发期间抑制气道高反应性和炎症,可能是一种有前途的哮喘治疗方法。

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