Anti-Inflammatory Effects of (9Z,11E)-13-Oxooctadeca-9,11-dienoic Acid (13-KODE) Derived from Salicornia herbacea L. on Lipopolysaccharide-Stimulated Murine Macrophage via NF-kB and MAPK Inhibition and Nrf2/HO-1 Signaling Activation

被引:12
|
作者
Ko, Yu-Chan [1 ]
Choi, Hack Sun [1 ,2 ,3 ,4 ]
Kim, Su-Lim [1 ,2 ,3 ,4 ]
Yun, Bong-Sik [5 ]
Lee, Dong-Sun [1 ,2 ,3 ,4 ,6 ]
机构
[1] Jeju Natl Univ, Interdisciplinary Grad Program Adv Convergence Te, Jeju 63243, South Korea
[2] Jeju Natl Univ, Subtrop Trop Organ Gene Bank, Jeju 63243, South Korea
[3] Jeju Natl Univ, Biohlth Mat Core Facil Ctr, Jeju 63243, South Korea
[4] Jeju Natl Univ, Pract Translat Res Ctr, Iksan 63243, South Korea
[5] Jeonbuk Natl Univ, Coll Environm & Bioresource Sci, Fac Div Biotechnol, Iksan 54596, South Korea
[6] Jeju Natl Univ, Coll Appl Life Sci, Fac Biotechnol, Jeju 63243, South Korea
基金
新加坡国家研究基金会;
关键词
(9Z; 11E)-13-Oxooctadeca-9; 11-dienoic acid (13-KODE); Salicornia herbacea L; inflammation; macrophage; antioxidant; OXIDATIVE STRESS; LINOLEIC-ACID; KAPPA-B; INFLAMMATORY RESPONSE; HEME OXYGENASE-1; DOWN-REGULATION; EXPRESSION; CELLS; POLYSACCHARIDES; INDUCTION;
D O I
10.3390/antiox11020180
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glasswort (Salicornia herbacea L.) is a halophyte that exhibits antioxidant and antidiabetic effects. Only a few studies have been conducted on its antioxidant effects. Here, we isolated an antioxidant using an activity-based purification method, and the resulting compound was identified as (9Z,11E)-13-Oxooctadeca-9,11-dienoic acid (13-KODE). We investigated its ability to suppress inflammatory responses and the molecular mechanisms underlying these abilities using lipopolysaccharide-stimulated RAW 264.7 macrophage cells. We studied the anti-inflammatory effects of 13-KODE derived from S. herbacea L on RAW 264.7 macrophages. 13-KODE inhibited lipopolysaccharide (LPS)-induced nitric oxide (NO) production by suppressing inducible NO synthase and suppressed LPS-induced tumor necrosis factor and interleukin-1 beta expression in RAW 264.7 macrophages. LPS-mediated nuclear localization of NF-kappa B and mitogen-activated protein kinase activation were inhibited by 13-KODE. 13-KODE significantly reduced LPS-induced production of reactive oxygen species and increased the expression of nuclear factor erythroid-2 like 2 (Nfe2I2) and heme oxygenase 1. Overall, our results indicate that 13-KODE may have potential for treating inflammation.
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页数:15
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