Effects of wogonin, a plant flavone from Scutellaria radix, on skin inflammation:: in vivo regulation of inflammation-associated gene expression

被引:191
作者
Chi, YS [1 ]
Lim, H [1 ]
Park, H [1 ]
Kim, HP [1 ]
机构
[1] Kangwon Natl Univ, Coll Pharm, Chunchon 200701, South Korea
关键词
flavonoid; wogonin; skin inflammation; cyclooxygenase; tumor necrosis factor; intercellular adhesion molecule;
D O I
10.1016/S0006-2952(03)00463-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Flavonoids from plant origin show anti-inflammatory activity in vitro and in vivo. In addition to inhibition of inflammation-associated enzymes, such as cyclooxygenases (COX) and lipoxygenases, they have been found to regulate the expression of inflammation-associated proteins from in vitro experiments. In order to prove in vivo behavior and the potential for beneficial use against inflammatory skin disorders, the effect of wogonin (5,7-dihydroxy-8-methoxyflavone) on in vivo expression of several inflammation-associated genes was examined in the intact as well as in the inflamed mouse skin by reverse transcriptase-polymerase chain reaction analysis. When applied topically on the intact skin, only a high dose treatment of wogonin (1000 mug/ear/3 days) slightly increased COX-1 and fibronectin mRNA. On the other hand, wogonin at the doses of 250-1000 mug/ear/3 days potently lowered mRNA levels of COX-2 and tumor necrosis factor-alpha with less effect on intercellular adhesion molecule-1 and interleukin-1beta in a sub-chronic skin inflammation model of tetradecanoylphorbol-13-acetate-induced ear edema (multiple treatment). The decrease of prostaglandin E-2 concentration (27.3-34.3%) was concomitantly observed in the wogonin-treated groups. A similar effect was also observed in an acute inflammation model of arachidonic acid-induced ear edema. From the present study, wogonin was proved to differentially regulate the expression of inflammation-associated genes in vivo and to become a useful therapeutic agent for skin inflammatory diseases mainly due to its modulation of the expression of proinflammatory molecules. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:1271 / 1278
页数:8
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