Simvastatin decreases IL-6 and IL-8 production in epithelial cells

被引:122
作者
Sakoda, K.
Yamamoto, M.
Negishi, Y.
Liao, J. K.
Node, K.
Izumi, Y.
机构
[1] Kagoshima Univ, Dept Periodontol, Grad Sch Med & Dent Sci, Kagoshima 8908544, Japan
[2] Showa Univ, Sch Dent, Dept Periodontol, Tokyo 142, Japan
[3] Tokyo Univ Pharm & Life Sci, Sch Pharm, Tokyo, Japan
[4] Brigham & Womens Hosp, Div Cardiovasc, Vasc Med Unit, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
[6] Saga Univ, Dept Cardiovasc & Renal Med, Fac Med, Saga 840, Japan
关键词
simvastatin (3-ydroxy-3-methylglutaryl co-enzyme A reductase inhibitor); pleiotropic effects; inflammatory cytokines; periodontitis; human oral epithelial cell;
D O I
10.1177/154405910608500608
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Many cardiovascular studies have suggested that 3-hydroxy-3-methylglutaryl co-enzyme A reductase inhibitors (statins) have anti-inflammatory effects independent of cholesterol lowering. As a chronic inflammatory disease, periodontitis shares some mechanisms with atherosclerosis. Since oral epithelial cells participate importantly in periodontal inflammation, we measured simvastatin effects on interleukin-6 and interleukin-8 production by cultured human epithelial cell line (KB cells) in response to interleukin-1 alpha. Simvastatin decreased production, an effect reversed by adding mevalonate or geranylgeranyl pyrophosphate, but not farnesyl pyrophosphate. Simvastatin was found to reduce NF-kappa B and AP-1 promoter activity in KB cells. Dominant-negative Rac1 severely inhibited interleukin-1 alpha-induced NF-kappa B and AP-1 promoter activity. Our results may indicate an anti-inflammatory effect of simvastatin on human oral epithelial cells, apparently involving Rac1 GTPase inhibition.
引用
收藏
页码:520 / 523
页数:4
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