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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 KaiWing 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.
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页码:624 / 631
页数:8
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