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CD4+CD25+Foxp3+ T cells contribute to the antiasthmatic effects of Astragalus membranaceus extract in a rat model of asthma

机译:CD4 + CD25 + Foxp3 + T细胞有助于哮喘大鼠模型中黄芪提取物的平喘作用

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Astragalus membranaceus (AM), a traditional Chinese medicinal herb, has been widely used for centuries to treat asthma in China. Previous studies demonstrated that AM had inhibitory effects on airway hyperresponsiveness, inflammation and airway remodeling in murine models of asthma. However, it remained unclear whether the beneficial effects of AM on asthma were associated with CD4+CD25+Foxp3+ Treg cells; this issue is the focus of the present work. An asthma model was established in Sprague-Dawley (SD) rats that were sensitized and challenged with ovalbumin. Bronchoalveolar lavage fluid (BALF) was assessed for inflammatory cell counts and cytokine levels. Airway hyperresponsiveness was detected by direct airway resistance analysis. Lung tissues were examined for cell infiltration, mucus hypersecretion and airway remodeling. CD4+CD25+Foxp3+ Treg cells in the BALF and Foxp3 mRNA expression in lung tissues were examined. The oral administration of AM significantly reduced airway hyperresponsiveness to aerosolized methacholine and inhibited eosinophil counts and reduced IL-4, IL-5 and IL-13 levels and increased INF-?? levels in the BALF. Histological studies showed that AM markedly decreased inflammatory infiltration, mucus secretion and collagen deposition in the lung tissues. Notably, AM significantly increased population of CD4+CD25+Foxp3+ Treg cells and promoted Foxp3+ mRNA expression in a rat model of asthma. Together, these results suggest that the antiasthmatic effects of AM are at least partially associated with CD4+CD25+Foxp3+ Tregs. ? 2012 Elsevier B.V. All rights reserved.
机译:黄芪(AM)是一种传统的中草药,已经在中国治疗哮喘已有数百年的历史了。先前的研究表明,AM对哮喘小鼠模型的气道高反应性,炎症和气道重塑具有抑制作用。然而,目前尚不清楚AM对哮喘的有益作用是否与CD4 + CD25 + Foxp3 + Treg细胞有关。这个问题是当前工作的重点。在Sprague-Dawley(SD)大鼠中建立了哮喘模型,并对其进行了卵白蛋白致敏和攻击。评估支气管肺泡灌洗液(BALF)的炎性细胞计数和细胞因子水平。通过直接气道阻力分析检测气道高反应性。检查肺组织的细胞浸润,粘液分泌过多和气道重塑。检查肺组织中BALF中的CD4 + CD25 + Foxp3 + Treg细胞和Foxp3 mRNA的表达。口服AM可显着降低气道对雾化乙酰甲胆碱的过敏反应,并抑制嗜酸性粒细胞计数,并降低IL-4,IL-5和IL-13水平,并增加INF-α? BALF中的级别。组织学研究表明,AM明显减少了肺组织中的炎症浸润,粘液分泌和胶原蛋白沉积。值得注意的是,在哮喘大鼠模型中,AM显着增加了CD4 + CD25 + Foxp3 + Treg细胞的数量并促进了Foxp3 + mRNA的表达。总之,这些结果表明AM的抗哮喘作用与CD4 + CD25 + Foxp3 + Tregs至少部分相关。 ? 2012 Elsevier B.V.保留所有权利。

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