Acteoside and 6-o-acetylacteoside downregulate cell adhesion molecules induced by IL-1beta; through inhibition of ERK and JNK in human vascular endothelial cells

Chao Hsiang Chen, Tuzz Ying Song, Y. U Chih Liang, H. U. Miao-Lin

研究成果: 雜誌貢獻文章同行評審

30 引文 斯高帕斯(Scopus)

摘要

Acteoside, an aclive phenylethanoid glycoside of many medicinal plants and bitter tea, displays antiinflammatory properties in vitro. However, it is unclear whether acteoside and similar compounds may inhibit the expression of cell adhesion molecules (CAMs), which plays a role in the pathogenesis of atherosclerosis and inflammation. Here, we found that acteoside, isoacteoside, and 6-O-acetylacteoside inhibited IL-1β-activated expression of intercellular CAM-1 (ICAM-1) and vascular CAM-1 (VCAM-1) in human umbilical vein endothelial cells (HUVECs); the inhibitory potency was as follows: 6-O-acetylacteoside > acteoside > isoacteoside. Acteoside and 6-O-acetylacteoside also dose-dependently inhibited VCAM-1 gene promoter activity in IL-1β-activated HUVECs. The inhibition of acteoside and 6-O-acetylacteoside on IL-1β-activated expression of CAMs was manifested by decreased phosphorylation of extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK). These results indicate that acteoside and 6-O-acetylacteoside may exert anti-inflammatory activities in vascular endothelium by inhibiting the expression of CAMs, primarily through decreased phosphorylation of ERK and JNK.
原文英語
頁(從 - 到)8852-8859
頁數8
期刊Journal of Agricultural and Food Chemistry
57
發行號19
DOIs
出版狀態已發佈 - 2009

ASJC Scopus subject areas

  • 農業與生物科學 (全部)
  • 化學 (全部)

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