Suppressive Effect of Tomentosin on the Production of Inflammatory Mediators in RAW264.7 Cells

被引:29
|
作者
Park, Hyo-Hyun [1 ]
Kim, Sun-Gun [1 ]
Kim, Mi Jin [2 ]
Lee, Jiean [3 ]
Choi, Bong-Keun [3 ]
Jin, Mei-Hua [4 ]
Lee, Eunkyung [1 ]
机构
[1] Korea Promot Inst Tradit Med Ind, Div Res & Dev, Gyongsan 712210, South Korea
[2] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[3] Myongji Univ, Ctr Nutraceut & Pharmaceut Mat, Yongin 449728, South Korea
[4] Tianjin Med Univ, Tianjin 300070, Peoples R China
关键词
tomentosin; inflammatory mediator; nuclear factor (NF)-kappa B; mitogen-activated protein (MAP) kinase; NF-KAPPA-B; NITRIC-OXIDE PRODUCTION; RAW; 264.7; CELLS; SIGNAL-TRANSDUCTION; THERAPEUTIC TARGET; MAPK INACTIVATION; COX-2; EXPRESSION; GENE-EXPRESSION; RAW-264.7; IN-VITRO;
D O I
10.1248/bpb.b14-00050
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In this study, tomentosin, a sesquiterpene lactone was isolated from Inulae fibs and its biological activities were investigated. The effects of tomentosin on the production of inflammatory mediators as well as on nuclear factor (NF)-kappa B and mitogen-activated protein (MAP) kinase activation were evaluated in RAW264.7 cells. Tomentosin decreased the production of nitric oxide (NO) and prostaglandin E-2 (PGE(2)) by suppressing the protein expression of inducible NO synthase (iNOS) and cyclooxygenase (COX)-2, respectively. Additionally, tomentosin reduced the release of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6). Tomentosin not only attenuated lipopolysaccharide (LPS)-induced NF-kappa B activation via the abrogation of inhibitory (I)kappa B alpha degradation and caused a subsequent decrease in nuclear p65 level, but it also suppressed the phosphorylation of MAP kinases (p38 and c-Jun N terminal kinase (JNK)). These results indicate that tomentosin exerts anti-inflammatory activities through the inhibition of inflammatory mediators (NO, iNOS, PGE(2), COX-2, TNF-alpha, and IL-6) by regulating NF-kappa B activation and phosphorylation of p38/JNK kinases in macrophages, thus suggesting that tomentosin could be a potential agent for the treatment of inflammatory diseases.
引用
收藏
页码:1177 / 1183
页数:7
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