Anti-inflammatory effect and action mechanisms of traditional herbal formula Gamisoyo-san in RAW 264.7 macrophages

被引:37
作者
Jin, Seong Eun [1 ]
Kim, Ohn Soon [2 ]
Yoo, Sae-Rom [1 ]
Seo, Chang-Seob [1 ]
Kim, Yeji [1 ,3 ]
Shin, Hyeun-Kyoo [1 ]
Jeong, Soo-Jin [2 ,4 ]
机构
[1] Korea Inst Oriental Med, K Herb Res Ctr, Daejeon 34054, South Korea
[2] Korea Inst Oriental Med, KM Convergence Res Div, 1672 Yuseong Daero, Daejeon 34054, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Mucosal Immunol Lab,Dept Convergence Med, Seoul 05505, South Korea
[4] Univ Sci & Technol, Korean Med Life Sci, Daejeon 34113, South Korea
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2016年 / 16卷
关键词
Gamisoyo-san; Inflammatory mediator; Cytokine; Mitogen-activated protein kinases (MAPKs); Nuclear transcription factor kappa B (NF-kappa B); NF-KAPPA-B; TUMOR-NECROSIS-FACTOR; NITRIC-OXIDE SYNTHASE; PROTEIN-KINASE PATHWAYS; IN-VITRO; INFLAMMATORY MEDIATORS; RAW264.7; MACROPHAGES; MURINE MACROPHAGES; GUIDED ISOLATION; MAPK ACTIVATION;
D O I
10.1186/s12906-016-1197-7
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Gamisoyo-san (GMSYS) is a traditional herbal formula used to treat insomnia, dysmenorrhea, and infertility in Korea. The purpose of this study was to investigate the anti-inflammatory effect and action mechanisms of GMSYS in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. Methods: The anti-inflammatory effects of GMSYS were investigated using nitric oxide (NO) assay and ELISAs for prostaglandin E-2 (PGE(2)), tumor necrosis factor-alpha (TNF-alpha), and interleukin-6 (IL-6). The anti-inflammatory action mechanisms of GMSYS were evaluated using Western blotting for inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and activation of nuclear transcription factor kappa B (NF-kappa B) and mitogen-activated protein kinases (MAPKs). Results: GMSYS significantly inhibited the LPS-induced production of NO, PGE(2), TNF-alpha, and IL-6 compared with the vehicle-treated cells. GMSYS consistently downregulated the expression of iNOS and COX-2 mRNA induced by LPS. In addition, pretreatment with GMSYS suppressed the LPS-induced activation of NF-kappa B and MAPKs such as p38, extracellular signal-regulated kinase (ERK), and c-Jun N-terminal kinase (JNK). Conclusions: Our results indicate that the anti-inflammatory effects of GMSYS in RAW 264.7 macrophages are associated with inhibition of the release of inflammatory mediators and cytokines through the suppression of MAPK and NF-kappa B activation. These findings suggest that GMSYS may be a useful therapeutic candidate for the prevention or treatment of inflammatory diseases.
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收藏
页数:11
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