2',4',6'-Tris(methoxymethoxy) chalcone protects against trinitrobenzene sulfonic acid-induced colitis and blocks tumor necrosis factor-α-induced intestinal epithelial inflammation via heme oxygenase 1-dependent and independent pathways

被引:89
|
作者
Lee, Sung Hee
Sohn, Dong Hwan
Jin, Xing Yu
Kim, Sang Wook
Choi, Suck Chei
Seo, Geom Seog [1 ]
机构
[1] Wonkwang Univ Sch Med, Digest Dis Res Inst, Iksan 570749, Jeonbuk, South Korea
[2] Wonkwang Univ, Coll Pharm, Iksan 570749, Jeonbuk, South Korea
[3] Chonnam Natl Univ, Coll Med, Dept Internal Med, Jeonju 561712, Jeonbuk, South Korea
关键词
2'; 4'; 6'-Tris(methoxymethoxy); chalcone; trinitrobenzene sulfonic acid; tumor necrosis factor-a; heme oxygenase 1; nuclear factor-kappa B;
D O I
10.1016/j.bcp.2007.06.034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
2',4',6'-Tris(methoxymethoxy) chalcone (TMMC), a synthesized chalcone derivative, displays potent antiproliferative and anti-inflammatory effects in rat hepatic stellate cells and murine macrophages, respectively. Here we tested the hypothesis that TMMC could ameliorate diseases characterized by mucosal inflammation. Treatment of mice with TMMC significantly protected against trinitrobenzene sulfonic acid (TNBS)-induced colitis, as assessed by reductions in the weight loss, colonic damage and mucosal ulceration that together characterize this symptom. Moreover, TMMC suppressed the expression of intercellular adhesion molecule-1, interleukin 10 (IL-1 beta) and tumor necrosis factor-alpha (TNF-alpha) in the mice treated with TNBS. Pretreatment of human intestinal epithelial HT-29 cells with TMMC also significantly inhibited the IL-8 and extracellular matrix metalloproteinase-7 levels induced by TNF-alpha. TMMC induced the expression of heme oxygenase 1 (HO-1) in HT-29 cells. TMMC increased extracellular signal-regulated kinase1/2 and p38 kinase phosphorylation levels, which led to the nuclear translocation of nuclear factor-erythroid 2-related factor 2 (Nrf2) and consequently to HO-1 expression. TMMC inhibited TNF-a -induced nuclear factor kappa B (NF-kappa B) activation directly and indirectly. Interestingly, the latter is mediated by HO-1, which presumably blocks the TNF-alpha-induced nuclear translocation of NF-kappa B p65 without affecting I-kappa B alpha. degradation. Moreover, we found that the different products of HO-1, carbon monoxide and bilirubin, exerted anti-inflammatory effects that were additive or synergistic in HT-29 cells stimulated with TNF-alpha. Thus, TMMC might serve to protect against intestinal inflammatory diseases. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:870 / 880
页数:11
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