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

Authors :
Yan-Fang Xian
Siu-Po Ip
Dian-Wei Wu
Jian-Hui Xie
Yu-Cui Li
Xiao-Ping Lai
Zi-Ren Su
Jin-Bin Liao
Zhi-Xiu Lin
Chuwen Li
Jian-Nan Chen
Source :
Journal of Ethnopharmacology. 157:212-221
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

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- κ 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 (LD 50 ) 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-α, IL-6, IL-1β, NO, and PGE 2 . The action mechanism of the anti-inflammatory activity of PO was partly dependent on inhibition of the activation of NF- κ B and the phosphorylation 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- κ B and the phosphorylation of p38 MAPK. Moreover, the LD 50 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.

Details

ISSN :
03788741
Volume :
157
Database :
OpenAIRE
Journal :
Journal of Ethnopharmacology
Accession number :
edsair.doi.dedup.....8313adb465218c7b19964abc1a2efb46
Full Text :
https://doi.org/10.1016/j.jep.2014.09.023