首页> 美国卫生研究院文献>Mediators of Inflammation >Illicium verum Extract and Trans-Anethole Attenuate Ovalbumin-Induced Airway Inflammation via Enhancement of Foxp3+ Regulatory T Cells and Inhibition of Th2 Cytokines in Mice
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Illicium verum Extract and Trans-Anethole Attenuate Ovalbumin-Induced Airway Inflammation via Enhancement of Foxp3+ Regulatory T Cells and Inhibition of Th2 Cytokines in Mice

机译:八角茴香提取物和反茴香通过增强Foxp3 +调节性T细胞和抑制Th2细胞因子来减轻卵清蛋白诱导的气道炎症。

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摘要

Illicium verum is used in traditional medicine to treat inflammation. The study investigates the effects of IVE and its component, trans-anethole (AET), on airway inflammation in ovalbumin- (OVA-) induced asthmatic mice. Asthma was induced in BALB/c mice by systemic sensitization to OVA, followed by intratracheal, intraperitoneal, and aerosol allergen challenges. IVE and AET were orally administered for four weeks. We investigated the effects of treatment on airway hyperresponsiveness, IgE production, pulmonary eosinophilic infiltration, immune cell phenotypes, Th2 cytokine production in bronchoalveolar lavage, Th1/Th2 cytokine production in splenocytes, forkhead box protein 3 (Foxp3) expression, and lung histology. IVE and AET ameliorated OVA-driven airway hyperresponsiveness (p < 0.01), pulmonary eosinophilic infiltration (p < 0.05), mucus hypersecretion (p < 0.01), and IL-4, IL-5, IL-13, and CCR3 production (p < 0.05), as well as IgE levels (p < 0.01). IVE and AET increased Foxp3 expression in lungs (p < 0.05). IVE and AET reduced IL-4 and increased IFN-γ production in the supernatant of splenocyte cultures (p < 0.05). Histological studies showed that IVE and AET inhibited eosinophilia and lymphocyte infiltration in lungs (p < 0.01). These results indicate that IVE and AET exert antiasthmatic effects through upregulation of Foxp3+ regulatory T cells and inhibition of Th2 cytokines, suggesting that IVE may be a potential therapeutic agent for allergic lung inflammation.
机译:八角茴香在传统医学中用于治疗炎症。该研究调查了IVE及其成分反式茴香脑(AET)对卵清蛋白(OVA-)诱发的哮喘小鼠气道炎症的影响。在BALB / c小鼠中,通过对OVA的全身致敏作用诱发哮喘,然后进行气管内,腹膜内和气溶胶过敏原攻击。 IVE和AET口服给药四个星期。我们调查了治疗对气道高反应性,IgE产生,肺嗜酸性粒细胞浸润,免疫细胞表型,支气管肺泡灌洗中Th2细胞因子产生,脾细胞Th1 / Th2细胞因子产生,叉头盒蛋白3(Foxp3)表达和肺组织学的影响。 IVE和AET改善了OVA驱动的气道高反应性(p <0.01),肺嗜酸性粒细胞浸润(p <0.05),粘液分泌过多(p <0.01)以及IL-4,IL-5,IL-13和CCR3产生(p <0.05)以及IgE水平(p <0.01)。 IVE和AET增加了肺中Foxp3的表达(p <0.05)。 IVE和AET降低了脾细胞培养上清液中的IL-4并增加了IFN-γ的产生(p <0.05)。组织学研究表明,IVE和AET抑制了肺中的嗜酸性粒细胞增多和淋巴细胞浸润(p <0.01)。这些结果表明,IVE和AET通过上调Foxp3 + 调节性T细胞和抑制Th2细胞因子发挥抗哮喘作用,提示IVE可能是过敏性肺炎症的潜在治疗剂。

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