Tomatidine inhibits iNOS and COX-2 through suppression of NF-κB and JNK pathways in LPS-stimulated mouse macrophages

被引:140
作者
Chiu, Feng-Lan [1 ]
Lin, Jen-Kun [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Inst Biochem & Mol Biol, Taipei 10018, Taiwan
关键词
tomatidine; iNOS; COX-2; NF-kappa B; JNK; AP-1; Oct-2;
D O I
10.1016/j.febslet.2008.05.049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We use the LPS-stimulated macrophage as a model of inflammation to investigate the anti-inflammatory effects of tomatidine and solasodine, whose structures resemble glucocorticoids. We found that tomatidine exhibited a more potent anti-inflammatory effect than solasodine. Tomatidine could decrease inducible nitric oxide synthase and cyclooxygenase-2 expression through suppression of I-kappa B alpha phosphorylation, NF-kappa B nuclear translocation and JNK activation, which in turn inhibits c-jun phosphorylation and Oct-2 expression. Here, we demonstrate that tomatidine acts as an anti-inflammatory agent by blocking NF-kappa B and JNK signaling, and may possibly be developed as a useful agent for the chemoprevention of cancer or in. ammatory diseases. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2407 / 2412
页数:6
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