首页> 外文期刊>Clinical and experimental allergy : >Five-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside attenuates poly (I:C)-induced airway inflammation in a murine model of asthma.
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Five-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside attenuates poly (I:C)-induced airway inflammation in a murine model of asthma.

机译:在小鼠哮喘模型中,五氨基咪唑-4-羧酰胺-1-β-4-呋喃呋喃糖苷可减轻聚(I:C)诱导的气道炎症。

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BACKGROUND: Asthma can frequently be induced or exacerbated by respiratory viral infections. Oxidative stress might also play an essential role in the pathogenesis of allergic airway diseases, indicating that antioxidant therapy may have a potential effect in controlling allergic airway diseases. Recent studies showed that 5-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside (AICAR) has the potential ability to modulate NADPH oxidase activity, indicating the antioxidant activity of AICAR. This study investigated the inhibitory effects of AICAR as an anti-inflammatory modulator on allergic airway inflammation in murine animal models. METHODS: The anti-inflammatory effects of AICAR were evaluated in two experimental asthma models: (1) an ovalbumin (OVA)-induced experimental asthma model and (2) an OVA plus polyinosinic-polycytidylic acid [poly (I:C)]-induced experimental asthma model to mimic respiratory viral infections. The inhibitory effects of AICAR in poly (I:C)-mediated signalling for NF-kappaB activation and production of TNF-alpha were analysed in vitro. RESULTS: AICAR was shown to have a marginal inhibitory effect in an OVA-induced asthma model. Interestingly, AICAR significantly attenuated poly (I:C)-induced airway hyperresponsiveness and airway inflammation, as shown by the attenuation of the influx of total inflammatory cells and soluble products into bronchoalveolar lavage fluid, such as macrophages, eosinophils, IL-5, IL-13, TNF-alpha and IFN-gamma. AICAR also significantly reduced the serum levels of OVA-specific IgE and IgG2a antibodies. Histologic and flow cytometric studies showed that AICAR inhibited poly (I:C)-induced lung inflammation and the infiltration of CD11b+CD11c+ dendritic cells into the lung. Moreover, AICAR effectively inhibited poly (I:C)-mediated activation of NF-kappaB and the production of TNF-alpha. CONCLUSION: These findings suggest that AICAR may be a novel immunomodulator with promising beneficial effects for the treatment of respiratory viral infection in airway allergic diseases.
机译:背景:呼吸道病毒感染经常会诱发或加剧哮喘。氧化应激也可能在过敏性气道疾病的发病机理中起重要作用,这表明抗氧化剂治疗可能在控制过敏性气道疾病中具有潜在作用。最近的研究表明,5-氨基咪唑-4-羧酰胺-1-β-4-核呋喃糖苷(AICAR)具有调节NADPH氧化酶活性的潜在能力,表明AICAR的抗氧化活性。这项研究调查了AICAR作为抗炎调节剂对鼠类动物模型中过敏性气道炎症的抑制作用。方法:在两个实验性哮喘模型中评估了AICAR的抗炎作用:(1)卵清蛋白(OVA)诱导的实验性哮喘模型,以及(2)OVA加多肌苷-聚胞苷酸[poly(I:C)]-诱导模拟哮喘病毒感染的实验性哮喘模型。在体外分析了AICAR在聚(I:C)介导的信号传导中对NF-κB活化和TNF-α的抑制作用。结果表明,在OVA诱发的哮喘模型中,AICAR具有边际抑制作用。有趣的是,AICAR显着减弱了聚(I:C)诱导的气道高反应性和气道炎症,如总炎症细胞和可溶性产物向支气管肺泡灌洗液(例如巨噬细胞,嗜酸性粒细胞,IL-5,IL)的流入减少所表明的那样。 -13,TNF-α和IFN-γ。 AICAR还显着降低了OVA特异性IgE和IgG2a抗体的血清水平。组织学和流式细胞术研究表明,AICAR抑制了聚(I:C)诱导的肺部炎症以及CD11b + CD11c +树突状细胞向肺的浸润。此外,AICAR有效抑制了聚(I:C)介导的NF-κB活化和TNF-α的产生。结论:这些发现表明,AICAR可能是一种新型的免疫调节剂,对治疗气道过敏性疾病的呼吸道病毒感染具有有益的有益作用。

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