Capillarisin inhibits iNOS, COX-2 expression, and proinflammatory cytokines in LPS-induced RAW 264.7 macrophages via the suppression of ERK, JNK, and NF-κB activation

被引:68
作者
Han, Suckbae [3 ,4 ]
Lee, Jong Hyun [3 ,4 ]
Kim, Chulwon [3 ,4 ]
Nam, Dongwoo [3 ,4 ]
Chung, Won-Seok [3 ,4 ]
Lee, Seok-Geun [3 ,4 ]
Ahn, Kyoo Seok [3 ,4 ]
Cho, Somi K. [5 ,6 ]
Cho, Moonjae [1 ,2 ]
Ahn, Kwang Seok [3 ,4 ]
机构
[1] Jeju Natl Univ, Dept Biochem, Sch Med, Cheju 690756, South Korea
[2] Jeju Natl Univ, Inst Med Sci, Cheju 690756, South Korea
[3] Kyung Hee Univ, Coll Oriental Med, Seoul, South Korea
[4] Kyung Hee Univ, Inst Oriental Med, Seoul, South Korea
[5] Jeju Natl Univ, Fac Biotechnol, Coll Appl Life Sci, Cheju 690756, South Korea
[6] Jeju Natl Univ, Subtrop Hort Res Inst, Cheju 690756, South Korea
关键词
Capillarisin; inflammation; NF-kappa B; nitric oxide; cyclooxygenase-2; NITRIC-OXIDE SYNTHASE; SIGNAL-REGULATED KINASE; TOLL-LIKE RECEPTORS; PROTEIN-KINASES; TRANSCRIPTION FACTOR; GENE-EXPRESSION; PATHWAYS; MECHANISMS; P38; LIPOPOLYSACCHARIDE;
D O I
10.3109/08923973.2012.736522
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The aerial parts of Artemisia capillaris (Compositae) have been used in traditional Korean medicine as a cholagogic, antipyretic, anti-inflammatory, and diuretic purposes. In our previous study, ethanolic extracts of the plant demonstrated a marked anti-inflammatory effect in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells (J. Korean Soc. Appl. Biol. Chem., 2010, 53, 275-282). In the present study, capillarisin (CPS), a flavone, main constituent of A. capillaris, was examined for its anti-inflammatory activity in the cells. We found that CPS highly suppressed LPS-induced nitric oxide (NO) without exerting cytotoxic effects on RAW 264.7 cells. CPS inhibited the expression of LPS-induced inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein and their mRNA in a dose-dependent manner. Also, tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, IL-1 beta, and prostaglandin E-2 (PGE(2)) secretion were decreased by CPS in LPS-stimulated macrophages. As a result, CPS inhibited proinflammatory cytokines, iNOS, and COX-2, which is attributed to the suppression of LPS-induced ERK, JNK, and nuclear factor-kappa B (NF-kappa B) activation. Therefore, we demonstrate here that CPS potentially inhibits the biomarkers related to inflammation through the abrogation of ERK, JNK, and NF-kappa B p65 activation, and it may be a potential therapeutic candidate for the treatment of inflammatory diseases.
引用
收藏
页码:34 / 42
页数:9
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