Costunolide alleviates HKSA-induced acute lung injury via inhibition of macrophage activation

被引:23
作者
Chen, Yun-tian [1 ]
Du, Yao [2 ]
Zhao, Bo [3 ]
Gan, Li-xing [1 ]
Yu, Kai-kai [3 ]
Sun, Lei [3 ]
Wang, Jian [1 ]
Qian, Feng [3 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Resp Med, Sch Med, Shanghai 200011, Peoples R China
[2] Fudan Univ, Peoples Hosp Shanghai 5, Dept Infect Dis, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Pharm, Minist Educ, Engn Res Ctr Cell & Therapeut Antibody, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Costunolide; Staphylococcus aureus; pneumonia; macrophage; MAPK signaling; EXPRESSION; PNEUMONIA; OPTIONS; MICE;
D O I
10.1038/s41401-018-0192-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Staphylococcus aureus (S. aureus) infection leads to a severe inflammatory response and causes acute lung injury (ALI), eventually threatening human life. Therefore, it is of importance to find an agent to inhibit inflammation and reduce ALI. Here, we found that costunolide, a sesquiterpene lactone, displays anti-inflammatory effects and ameliorates heat-killed S. aureus (HKSA)-induced pneumonia. Costunolide treatment attenuated HKSA-induced murine ALI in which pulmonary neutrophil infiltration was inhibited, lung edema was decreased, and the production of pro-inflammatory cytokines was significantly reduced. In addition, costunolide dose-dependently inhibited the generation of IL-6, TNF-alpha, IL-1 beta, and keratinocyte-derived cytokine (KC), as well as the expression of iNOS, in HKSA-induced macrophages. Furthermore, costunolide attenuated the phosphorylation of p38 MAPK and cAMP response element-binding protein (CREB). Collectively, our findings suggested that costunolide is a promising agent for alleviating bacterial-induced ALI via the inhibition of the MAPK signaling pathways.
引用
收藏
页码:1040 / 1048
页数:9
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