青蒿琥酯
蛋白激酶B
支气管肺泡灌洗
PI3K/AKT/mTOR通路
药理学
医学
嗜酸性粒细胞
嗜酸性粒细胞趋化因子
免疫学
卵清蛋白
生物
肺
哮喘
信号转导
内科学
恶性疟原虫
免疫系统
生物化学
疟疾
作者
Cheng Chang,Wanxing Eugene Ho,Fera Y. Goh,Shou Ping Guan,Li Kong,Wen-Qi Lai,Bernard P. Leung,W.S. Fred Wong
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2011-06-09
卷期号:6 (6): e20932-e20932
被引量:106
标识
DOI:10.1371/journal.pone.0020932
摘要
Background Phosphoinositide 3-kinase (PI3K)/Akt pathway is linked to the development of asthma. Anti-malarial drug artesunate is a semi-synthetic derivative of artemisinin, the principal active component of a medicinal plant Artemisia annua, and has been shown to inhibit PI3K/Akt activity. We hypothesized that artesunate may attenuate allergic asthma via inhibition of the PI3K/Akt signaling pathway. Methodology/Principal Findings Female BALB/c mice sensitized and challenged with ovalbumin (OVA) developed airway inflammation. Bronchoalveolar lavage fluid was assessed for total and differential cell counts, and cytokine and chemokine levels. Lung tissues were examined for cell infiltration and mucus hypersecretion, and the expression of inflammatory biomarkers. Airway hyperresponsiveness was monitored by direct airway resistance analysis. Artesunate dose-dependently inhibited OVA-induced increases in total and eosinophil counts, IL-4, IL-5, IL-13 and eotaxin levels in bronchoalveolar lavage fluid. It attenuated OVA-induced lung tissue eosinophilia and airway mucus production, mRNA expression of E-selectin, IL-17, IL-33 and Muc5ac in lung tissues, and airway hyperresponsiveness to methacholine. In normal human bronchial epithelial cells, artesunate blocked epidermal growth factor-induced phosphorylation of Akt and its downstream substrates tuberin, p70S6 kinase and 4E-binding protein 1, and transactivation of NF-κB. Similarly, artesunate blocked the phosphorylation of Akt and its downstream substrates in lung tissues from OVA-challenged mice. Anti-inflammatory effect of artesunate was further confirmed in a house dust mite mouse asthma model. Conclusion/Significance Artesunate ameliorates experimental allergic airway inflammation probably via negative regulation of PI3K/Akt pathway and the downstream NF-κB activity. These findings provide a novel therapeutic value for artesunate in the treatment of allergic asthma.
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