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Differential Effects of Dexamethasone and Itraconazole on Aspergillus fumigatus-Exacerbated Allergic Airway Inflammation in a Murine Model of Mite-Sensitized Asthma

机译:地塞米松和伊曲康唑对小鼠致敏性哮喘小鼠模型中烟曲霉加剧过敏性气道炎症的不同影响

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摘要

Background: Fungal exposure is associated with particularly severe asthma. Nevertheless, the effects of anti-fungal treatments on fungus-exacerbated asthma need to be determined. Objectives: The present study aimed to compare the effects of itraconazole (ITCZ) and dexamethasone (Dex) on Aspergillus fumigatus (Af)-exacerbated preexisting Dermatophagoides farinae (Df) allergen-sensitized allergic airway inflammation. Methods: Four groups of BALB/c mice were prepared: control, Df-sensitized plus Af-infected mice (Df-Af), and Df-Af mice treated with Dex (Df-Af-Dex) or with ITCZ (Df-Af-ITCZ). Pulmonary pathology and cytokine profiles in the airway were evaluated. In a different set of experiments, the effects of Dex on alveolar macrophage (AM) phagocytosis of Af conidia were determined in Df-sensitized mice. Results:Af infection significantly increased the level of eosinophils and neutrophils in the airway of Df-sensitized mice. While Dex significantly decreased eosinophils, ITCZ significantly decreased both eosinophils and neutrophils in Df-Af mice. Dex significantly decreased IL-5, whereas ITCZ significantly reduced MIP-2 in the airway. Compared to controls, AM isolated from Df-sensitized mice had significantly reduced phagocytotic activity of Af conidia. However, Dex significantly improved phagocytotic activity of AM in Df-sensitized mice. Conclusions: The present study showed that Dex and ITCZ differently regulated Af-exacerbated allergic airway inflammation; the former inhibits eosinophilic inflammation and the latter inhibits neutrophilic as well as eosinophilic inflammation by regulating different cytokines. Additionally, Dex enhanced the phagocytotic activity of AM in allergic asthma. Thus, a combination of Dex and ITCZ might be effective for the management of fungus-exacerbated asthma.
机译:背景:真菌暴露与特别严重的哮喘有关。然而,需要确定抗真菌治疗对真菌加重哮喘的作用。目的:本研究旨在比较伊曲康唑(ITCZ)和地塞米松(Dex)对烟曲霉(Af)加重的预先存在的Dermatophagoides farinae(Df)变应原致敏的过敏性气道炎症的影响。方法:制备四组BALB / c小鼠:对照,Df致敏加Af感染的小鼠(Df-Af)和用Dex(Df-Af-Dex)或ITCZ(Df-Af)治疗的Df-Af小鼠-ITCZ)。评估气道中的肺部病理学和细胞因子谱。在另一组不同的实验中,在Df致敏的小鼠中确定了Dex对Af分生孢子的肺泡巨噬细胞(AM)吞噬作用的影响。结果:Af感染显着增加Df致敏小鼠气道中的嗜酸性粒细胞和中性粒细胞水平。尽管Dex显着降低了嗜酸性粒细胞,但ITCZ显着降低了Df-Af小鼠的嗜酸性粒细胞和嗜中性粒细胞。 Dex显着降低了IL-5,而ITCZ显着降低了气道中的MIP-2。与对照组相比,从Df致敏小鼠中分离出的AM显着降低了Af分生孢子的吞噬活性。但是,Dex可以显着改善Df致敏小鼠中AM的吞噬活性。结论:本研究表明Dex和ITCZ对Af加重的过敏性气道炎症的调节不同。前者通过调节不同的细胞因子抑制嗜酸性粒细胞炎症,而后者抑制嗜中性粒细胞以及嗜酸性粒细胞炎症。此外,Dex增强了过敏性哮喘中AM的吞噬活性。因此,Dex和ITCZ的组合可能对于控制真菌加剧的哮喘有效。

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