Young Yum pill inhibits inflammatory mediators and nuclear factor-kappa B signaling in lipopolysaccharide-stimulated RAW 264.7 macrophages

被引:0
|
作者
Yin Chengle [1 ]
Muhammad Jahangir Hossen [1 ]
Anfernee Kai-Wing Tse [1 ]
Su Tao [1 ]
Fu Xiuqiong [1 ]
Li Ting [1 ]
Guo Hui [1 ]
Zhu Peili [1 ]
Li Junkui [1 ]
Chou Jiyao [1 ]
Wang Yaping [1 ]
Yu Zhiling [2 ,1 ]
机构
[1] Centre for Cancer and Inflammation Research, School of Chinese Medicine, Hong Kong Baptist University
[2] Research and Development Centre for Natural Health Products, Hong Kong Baptist University Shenzhen Research Institute and Continuing Education
关键词
Inflammation; NF-kappa B; Lipopolysaccharides; RAW; 264.7; cells; Macrophages; Young Yum pill;
D O I
10.19852/j.cnki.jtcm.2019.05.003
中图分类号
R285 [中药药理学];
学科分类号
1008 ;
摘要
OBJECTIVE: To investigate the effect of Young Yum pill(YYP) on inflammatory mediators in cultured RAW 264.7 cells and elucidate the nuclear factorkappa B(NF-κB)-related mechanism behind the action.METHODS: YYP was extracted with 95% ethanol Lipopolysaccharide(LPS)-stimulated RAW 264.7 macrophages were used to evaluate the effect of YYP on inflammatory mediators.Production of nitric oxide(NO) and prostaglandin E2(PGE2) were measured by Griess test and enzyme-linked immunosorbent assay, respectively.The levels of genes and proteins involved in the generation of inflammatory mediators were examined using real-time polymerase chain reaction and Western blotting, respectively.RESULTS: YYP dose-dependently suppressed LPSinduced production of NO, PGE2 and tumor necrosis factor-α(TNF-α), and elevation of mRNA and protein levels of inducible NO synthase and cyclooxygenase-2 in RAW 264.7 macrophages.These observations were associated with decreased NF-κB p65 phosphorylation and nuclear localization, enhanced Akt(protein kinase B) phosphorylation, as well as reduced inhibitor of κB(IκB) α degradation and IκB kinase α/β phosphorylation.CONCLUSION: The present study demonstrated an inhibitory effect of YYP on the NF-κB-regulated inflammatory mediators NO, PGE2 and TNF-α in LPSstimulated RAW 264.7 macrophages, providing a pharmacological basis for the use of YYP in treating inflammatory disorders.
引用
收藏
页码:624 / 631
页数:8
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