Anti-Malarial Drug Artesunate Attenuates Experimental Allergic Asthma via Inhibition of the Phosphoinositide 3-Kinase/Akt Pathway

被引:110
作者
Cheng, Chang [1 ,3 ]
Ho, W. Eugene [1 ,3 ]
Goh, Fera Y. [1 ,3 ]
Guan, Shou Ping [1 ,3 ]
Kong, Li Ren [1 ]
Lai, Wen-Qi [2 ]
Leung, Bernard P. [2 ]
Wong, W. S. Fred [1 ,3 ]
机构
[1] Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[2] Natl Univ Hlth Syst, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
[3] Natl Univ Singapore, Inst Life Sci, Program Immunol, Singapore 117548, Singapore
关键词
NF-KAPPA-B; GROWTH-FACTOR RECEPTOR; NITRIC-OXIDE SYNTHASE; AIRWAY SMOOTH-MUSCLE; ANTIINFLAMMATORY ROLE; EPITHELIAL-CELLS; TNF-ALPHA; IN-VITRO; INFLAMMATION; MICE;
D O I
10.1371/journal.pone.0020932
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
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-kappa B. 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-kappa B activity. These findings provide a novel therapeutic value for artesunate in the treatment of allergic asthma.
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页数:9
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