Isoegomaketone Inhibits Lipopolysaccharide-Induced Nitric Oxide Production in RAW 264.7 Macrophages through the Heme Oxygenase-1 Induction and Inhibition of the Interferon-β-STAT-1 Pathway

被引:42
作者
Jin, Chang Hyun [1 ]
Lee, Hyo Jung [2 ]
Park, Yong Dae [1 ]
Choi, Dae Seong [1 ]
Kim, Dong Sub [1 ]
Kang, Si-Yong [1 ]
Seo, Kwon-Il [3 ]
Jeong, Il Yun [1 ]
机构
[1] Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeonbuk, South Korea
[2] Gwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
[3] Sunchon Natl Univ, Dept Food & Nutr, Sunchon 540742, South Korea
关键词
Isoegomaketone; nitric oxide; lipopolysaccharide; STAT-1; heme oxygenase-1; NF-KAPPA-B; GENE-EXPRESSION; ALPHA; BETA; PHOSPHORYLATION; ACTIVATION; MECHANISMS; SYNTHASE; SIGNALS; CELLS;
D O I
10.1021/jf9033333
中图分类号
S [农业科学];
学科分类号
082806 [农业信息与电气工程];
摘要
Isoegomaketone (IK) is an essential oil component of Perilla frutescens (L.) Britt., and there have been no studies investigating its biological activities. We found that IK inhibits lipopolysaccharide (LPS)-induced nitric oxide (NO) production in RAW 264.7 macrophages, and moreover, when IK was injected into animals prior to LPS administration, NO serum levels decreased in a dose-dependent manner. These results indicate that IK possesses anti-inflammatory activity both in vitro and in vivo. IK suppressed the phosphorylation of STAT-1 and the production of IFN-beta. Treatment with IK also inhibited the activation of NF-kappa B and activator protein-1, but more IK was required for inhibition than for STAT-1 inhibition, indicating that downregulation of inducible nitric oxide synthase gene expression by IK is mainly attributed to the blockade of STAT-1 activation. Furthermore, IK also induced the expression of heme oxygenase-1 (HO-1) through the activation of nuclear factor E2-related factor 2. Treatment with SnPP, a selective inhibitor of HO-1, reversed the IK-induced suppression of STAT-1 phosphorylation and NO production. Taken together, IK isolated from P. frutescens inhibits NO production in LPS-treated RAW 264.7 macrophages through simultaneous induction of HO-1 and inhibition of the IFN-beta-STAT-1 pathway.
引用
收藏
页码:860 / 867
页数:8
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