Anti-inflammatory Activity of 3,6,3′-Trihydroxyflavone in Mouse Macrophages, In vitro

被引:4
作者
Lee, Eunjung [1 ]
Jeong, Ki-Woong [1 ]
Shin, Areum [1 ]
Kim, Yangmee [1 ]
机构
[1] Konkuk Univ, Inst KU Biotechnol, Dept Biosci & Biotechnol, Biomol Informat Ctr, Seoul 143701, South Korea
基金
新加坡国家研究基金会;
关键词
Anti-inflammatory activity; 3,6,3 '-Trihydroxyflavone; Flavonoid; JNK; Binding model; ACTIVATED RECEPTOR-GAMMA; NITRIC-OXIDE; MAP KINASES; CANCER; CELLS; INFLAMMATION; FLAVONOIDS; AMENTOFLAVONE; EXPRESSION; INHIBITORS;
D O I
10.5012/bkcs.2014.35.11.3169
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Numerous studies have examined the role of flavonoids in modulating inflammatory responses in vitro. In this study, we found a novel flavonoid, 3,6,3'-trihydroxyflavone (1), with anti-inflammatory effects. Antiinflammatory activity and mechanism of action were examined in mouse macrophages stimulated with lipopolysaccharide (LPS). Our results showed that the anti-inflammatory effects of 1 are mediated via p38 mitogen-activated protein kinase (08 MAPK), Jun-N terminal kinase (JNK), and the extracellular-signal-regulated kinase (ERK) pathway in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Binding studies revealed that 1 had a high binding affinity to JNK 1 (1.568 x 10(8) M-1) and that the 3- and 6-hydroxyl groups of the C-ring and A-ring of 1 participated in hydrogen bonding interactions with the side chains of Asnl14 and Lys55, respectively. The oxygen at the 3' position of the B-ring formed a hydrogen bond with side chain of Met111. Therefore, 1 could be a potential inhibitor of JNKs, with potent anti-inflammatory activity.
引用
收藏
页码:3169 / 3174
页数:6
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