Pogostone suppresses proinflammatory mediator production and protects against endotoxic shock in mice

被引:36
作者
Li, Yu-Cui [1 ]
Xian, Yan-Fang [2 ]
Su, Zi-Ren [1 ]
Ip, Siu-Po [2 ]
Xie, Jian-Hui [1 ]
Liao, Jin-Bin [1 ]
Wu, Dian-Wei [1 ]
Li, Chu-Wen [1 ]
Chen, Jian-Nan [1 ,3 ]
Lin, Zhi-Xiu [2 ]
Lai, Xiao-Ping [1 ,3 ]
机构
[1] Guangzhou Univ Chinese Med, Coll Chinese Med, Guangzhou Higher Educ Mega Ctr, Guangzhou 510006, Guangdong, Peoples R China
[2] Chinese Univ Hong Kong, Fac Med, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[3] Guangzhou Univ Chinese Med, Acad Chinese Med, Dongguan Math Engn, Dongguan 523808, Peoples R China
基金
中国国家自然科学基金;
关键词
Pogostone; Anti-inflammatory property; Inflammatory mediators; NF-kappa B; MAPKs; NF-KAPPA-B; INFLAMMATORY MEDIATORS; POGOSTEMONIS HERBA; LPS; LIPOPOLYSACCHARIDE; ACTIVATION; MECHANISMS; MACROPHAGES; MORTALITY; SYNTHASE;
D O I
10.1016/j.jep.2014.09.023
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Pogostemon cablin (Blanco) Benth is a well-known medicinal herb commonly used in many Asian countries for inflammatory diseases. Pogostone (PO), a natural product isolated from Pogostemon cablin, is known to exert various pharmacological activities. This study aimed to investigate the anti-inflammatory property of PO, to elucidate its mechanism of action, and to evaluate its potential acute toxicity. Materials and methods: The in vitro anti-inflammatory activity of PO was assessed using lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. The protein and mRNA levels of proinflammatory mediators were measured with ELISA and RT-PCR, respectively. Proteins of the NF-kappa B and MAPK family were determined by Western blot to investigate the underlying molecular mechanisms. The in vivo anti-inflammatory activity of PO was tested using LPS-induced endotoxic shock in mice. In addition, the median lethal dose (LD50) of PO in mice was tested in an acute toxicity test. Results: In vitro, PO significantly inhibited the protein and mRNA expression of proinflammatory mediators including TNF-alpha, IL-6, IL-1 beta, NO, and PGE(2). The action mechanism of the anti-inflammatory activity of PO was partly dependent on inhibition of the activation of NF-kappa B and the phosphotylation of JNK and p38 MAPK. In vivo, PO was able to significantly reduce the mortality induced by LPS in mice. Furthermore, PO could markedly suppress the production of the proinflammatory mediators in serum, and attenuate liver and lung injury. The action mechanisms of PO during endotoxic shock may be attributed to down-regulation of the mRNA expression of inflammatory mediators in multiple organs via inhibition of the activation of NF-kappa B and the phosphorylation of p38 MAPK Moreover, the LD50 of PO in mice was about 163 mg/kg with intravenous administration, which was about 8-fold higher than the dose used in the animal experiment. Conclusions: Our findings regarding the anti-inflammatory effect of PO and the underlying molecular mechanisms help justify the use of Pogostemon cablin in Chinese medicine for the treatment of inflammatory diseases. More importantly, the results also render PO a promising anti-inflammatory agent worthy of further development into a pharmaceutical drug for the treatment of septic shock. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:212 / 221
页数:10
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