Anti-inflammatory activity of Sorbus commixta water extract and its molecular inhibitory mechanism

被引:62
|
作者
Yu, Tao [2 ]
Lee, Yong Jin [3 ]
Jang, Hyun-Jae [4 ]
Kim, Ae Ra [5 ]
Hong, Sungyoul [2 ]
Kim, Tae Woong [4 ]
Kim, Mi-Yeon [6 ]
Lee, Jaehwi [1 ]
Lee, Yong Gyu [7 ]
Cho, Jae Youl [2 ]
机构
[1] Chung Ang Univ, Coll Pharm, Seoul 156756, South Korea
[2] Sungkyunkwan Univ, Dept Genet Engn, Suwon 440746, South Korea
[3] Chuncheon Bioind Fdn, Chunchon 200161, South Korea
[4] Kangwon Natl Univ, Dept Biochem, Chunchon 200701, South Korea
[5] Kangwon Natl Univ, Coll Pharm, Chunchon 200701, South Korea
[6] Soongsil Univ, Sch Syst Biol Sci, Seoul 156743, South Korea
[7] Kangwon Natl Univ, Coll Biomed Sci, Chunchon 200701, South Korea
关键词
Sorbus commixta; Macrophages; Inflammatory mediators; NF-kappa B translocation; Src and Syk activation; NF-KAPPA-B; METHANOL EXTRACT; VASCULAR INFLAMMATION; IN-VITRO; ACTIVATION; IDENTIFICATION; KINASE; CORTEX; PATHWAYS; LUPEOL;
D O I
10.1016/j.jep.2010.12.032
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological significance: Sorbus commixta Hedl. (Rosaceae) is a well known traditionally valuable medicinal plant in Korea, China and Japan. This plant has been prescribed for long time for various inflammatory symptoms such as asthma, bronchitis, gastritis and dropsy. Aim of study: Although a number of pharmacological properties have already been demonstrated, the anti-inflammatory effect of this plant and its associated molecular mechanisms has not yet been fully investigated. Materials and methods: In order to address the anti-inflammatory activity of S. commixta water extract (Sc-WE), lipopolysaccharide (LPS)-stimulated macrophages were employed and production of inflammatory mediators by these cells were evaluated. Results: Sc-WE significantly suppressed the production of nitric oxide (NO) and prostaglandin (PG)E-2 in a dose-dependent manner and blocked ear edema formation induced by arachidonic acid in mouse. In addition, this extract effectively diminished the mRNA levels of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2, indicating that the inhibition occurs at the transcriptional level. Interestingly, Sc-WE remarkably blocked NF-kappa B translocation and its upstream signaling events by inhibition of kappa B alpha (I kappa B alpha), I kappa B alpha kinase (IKK), Akt (protein kinase B), phosphoinositide-dependent kinase 1 (PDK1), p85/phosphoinositide-3-kinase (PI3K), as per the results obtained from the reporter gene assay and immunoblotting analysis. More intriguingly, Sc-WE suppressed activities of Src and Syk kinases as well as their phosphorylation levels without altering molecular complex formation between them and toll like receptor (TLR)4 or MyD88, an adaptor protein of TLR4-mediated signaling. Conclusion: Therefore, our results suggest that Sc-WE can be developed as a potent anti-inflammatory remedy, acting by suppressing the inflammatory signaling cascade composed of Src, Syk, and NF-kappa B. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:493 / 500
页数:8
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