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刺蕊草醇抑制促炎介质的产生并保护小鼠免受内毒素休克。

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

作者信息

Li Yu-Cui, Xian Yan-Fang, Su Zi-Ren, Ip Siu-Po, Xie Jian-Hui, Liao Jin-Bin, Wu Dian-Wei, Li Chu-Wen, Chen Jian-Nan, Lin Zhi-Xiu, Lai Xiao-Ping

机构信息

College of Chinese Medicines, Guangzhou University of Chinese Medicine, 232 Wai Huan Dong Road, Guangzhou Higher Education Mega Center, Guangzhou 510006, PR China.

School of Chinese Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, PR China.

出版信息

J Ethnopharmacol. 2014 Nov 18;157:212-21. doi: 10.1016/j.jep.2014.09.023. Epub 2014 Sep 26.

DOI:10.1016/j.jep.2014.09.023
PMID:25256685
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-κB 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-α, IL-6, IL-1β, NO, and PGE2. The action mechanism of the anti-inflammatory activity of PO was partly dependent on inhibition of the activation of NF-κB 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-κB and the phosphorylation of p38 MAPK. Moreover, the LD50 of PO in mice was about 163mg/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.

摘要

民族药理学相关性

广藿香是一种著名的药草,在许多亚洲国家常用于治疗炎症性疾病。从广藿香中分离出的天然产物广藿香酮(PO)具有多种药理活性。本研究旨在探讨PO的抗炎特性,阐明其作用机制,并评估其潜在的急性毒性。

材料与方法

使用脂多糖(LPS)刺激的RAW264.7巨噬细胞评估PO的体外抗炎活性。分别用ELISA和RT-PCR检测促炎介质的蛋白质和mRNA水平。通过蛋白质印迹法测定NF-κB和MAPK家族的蛋白质,以研究潜在的分子机制。使用LPS诱导的小鼠内毒素休克测试PO的体内抗炎活性。此外,在急性毒性试验中测试了PO在小鼠中的半数致死剂量(LD50)。

结果

在体外,PO显著抑制促炎介质包括TNF-α、IL-6、IL-1β、NO和PGE2的蛋白质和mRNA表达。PO抗炎活性的作用机制部分依赖于对NF-κB激活以及JNK和p38 MAPK磷酸化的抑制。在体内,PO能够显著降低LPS诱导的小鼠死亡率。此外,PO可显著抑制血清中促炎介质的产生,并减轻肝肺损伤。PO在内毒素休克期间的作用机制可能归因于通过抑制NF-κB激活和p38 MAPK磷酸化,下调多个器官中炎症介质的mRNA表达。此外,PO静脉注射小鼠的LD50约为163mg/kg,比动物实验中使用的剂量高约8倍。

结论

我们关于PO抗炎作用及其潜在分子机制的研究结果有助于证明广藿香在中医中用于治疗炎症性疾病的合理性。更重要的是,这些结果也使PO成为一种有前景的抗炎剂,值得进一步开发成治疗脓毒症休克用药。

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