Sentulic acid isolated from Sandoricum koetjape Merr attenuates lipopolysaccharide and interferon gamma co-stimulated nitric oxide production in murine macrophage RAW264 cells

被引:5
作者
Itoh, Tomohiro [1 ]
Katsurayama, Kousuke [1 ]
Efdi, Mai [2 ]
Ninomiya, Masayuki [3 ]
Koketsu, Mamoru [3 ]
机构
[1] Mie Univ, Grad Sch Bioresources, Dept Life Sci, Lab Mol Chem Aquat Mat, 1577 Kurimamachiya, Tsu, Mie 5148507, Japan
[2] Univ Andalas, Fac Math & Nat Sci, Dept Chem, Liman Minis 25163, Padang, Indonesia
[3] Gifu Univ, Fac Engn, Dept Chem & Biomol Sci, 1-1 Yanagido, Gifu 5011193, Japan
关键词
Sentulic acid; Sandrocum koetkape Merr; RAW264.7; cells; Nitric oxide; Toll-like receptor 4; INDUCED NO PRODUCTION; NF-KAPPA-B; URSOLIC ACID; HEME OXYGENASE-1; MAPK PATHWAYS; EXPRESSION; BINDING; MICE; LPS; SUPPRESSES;
D O I
10.1016/j.bmcl.2018.10.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A seco-triterpenoid, sentulic acid (SA) isolated from Sandoricum koetjape Merr attenuated nitric oxide (NO) production following co-stimulation with lipopolysaccharide (LPS) and interferon-gamma (IFN gamma) in RAW264.7 macrophage cells. The mRNA expression levels of proinflammatory cytokines such as tumor necrosis factor-alpha (TNF-alpha), IFN gamma, interleukin (IL)-6, and IL-12 in LPS/IFN gamma co-stimulated RAW264.7 cells also decreased upon SA treatment. To determine the molecular mechanisms underlying the inhibitory effect of SA on LPS/IFN gamma-induced NO production in RAW264.7 cells, we further analyzed Toll-like receptor (TLR) signaling by western blotting. The expression of TLR4 and IFN signaling molecules in cells treated with SA was significantly suppressed compared to that in cells not treated with SA. Additionally, SA inhibited the binding of LPS to the TLR4 receptor in RAW264.7 cells stimulated with Alexa Fluor 488-conjugated LPS. These results demonstrate that SA attenuates NO production after LPS/IFN gamma co-stimulation in RAW264.7 cells by inhibiting the binding of LPS to TLR4. Our findings suggest that SA is beneficial for the treatment of inflammatory diseases.
引用
收藏
页码:3496 / 3501
页数:6
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