KMID : 1161420110140040377
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Journal of Medicinal Food 2011 Volume.14 No. 4 p.377 ~ p.385
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Phenethyl Isothiocyanate Inhibits 12-O-Tetradecanoylphorbol-13-Acetate-Induced Inflammatory Responses in Mouse Skin
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Lee Yeo-Myeong
Cho Han-Jin Ponnuraj Shree Priya Kim Jong-Dai Kim Jong-Sang Kim Sang-Geon Park Jung-Han-Yoon
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Abstract
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Phenethyl isothiocyanate (PITC) is the hydrolysis product of the glucosinolate gluconasturtiin in cruciferous vegetables. This study was conducted to determine whether PITC inhibits 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced inflammation in the mouse ear. Topical application of 5?nmol of TPA to mouse ears markedly increased the ear weight, expression of the inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 protein, and phosphorylation of the inhibitor of ¥êB (I¥êB) ¥á, AKT, and extracellular signal-regulated protein kinase (ERK) 1/2 and reduced I¥êB¥á protein levels. Pretreatment with PITC (150?450?nmol) significantly suppressed these TPA-induced inflammatory responses. We also determined whether low concentrations of PITC (0.5?5?¥ìmol/L) inhibited lipopolysaccharide (LPS)-stimulated inflammatory responses in Raw264.7?cells. PITC dose-dependently reduced the LPS-induced secretion of nitric oxide, prostaglandin E2, interleukin (IL)-1¥â, IL-6, and tumor necrosis factor (TNF)-¥á, as well as COX-2 and iNOS protein expression. PITC also attenuated LPS-induced increases in iNOS, COX-2, IL- 6, IL-1¥â, and TNF-¥á mRNA levels, as well as the promoter-dependent transcriptional activation of the genes for iNOS and COX-2. PITC inhibited LPS-induced I¥êB¥á phosphorylation and degradation and subsequently reduced LPS-induced p65 nuclear translocation and the transcriptional activity of nuclear factor-¥êB (NF-¥êB), which was accompanied by a reduction in ERK1/2 and AKT phosphorylation. The results of this study demonstrated that PITC effectively inhibits inflammatory responses in vivo and in vitro, which may be mediated via the inhibition of AKT and ERK1/2 activation, leading to subsequent inhibition of the transcriptional activity of NF-¥êB.
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KEYWORD
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cyclooxygenase-2, inducible nitric oxide synthase, inflammation, nuclear factor-¥êB, phenethyl isothiocyanate
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