Ginsenoside Rg3 inhibits tumor necrosis factor-α-induced expression of cell adhesion molecules in human endothelial cells

被引:24
作者
Hien, Tran Thi [1 ]
Kim, Nak Doo [2 ]
Kim, Hyung Sik [3 ]
Kang, Keon Wook [1 ]
机构
[1] Chosun Univ, Coll Pharm, Project Team BK21, Kwangju 501759, South Korea
[2] Seoul Natl Univ, Seoul, South Korea
[3] Pusan Natl Univ, Coll Pharm, Pusan, South Korea
来源
PHARMAZIE | 2010年 / 65卷 / 09期
关键词
NF-KAPPA-B; TRANSCRIPTIONAL REGULATION; ACTIVATION; DISEASE; ATHEROSCLEROSIS; CYTOKINES; PATTERNS; RG(3); GENE;
D O I
10.1691/ph.2010.0569
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Ginsenoside Rg3 (Rg3), one of the most effective ginseng saponins, has anti-inflammatory and anti-cancer effects. This study examined the effects of Rg3 on cytokine-induced expression of adhesion molecules, which is a key early event in atherogenesis. Rg3 treatment inhibited tumor necrosis factor-alpha (TNF-alpha)-induced protein and mRNA expression of two cell adhesion molecules, vascular cell adhesion molecule-1 (VCAM-1) and intercellular cell adhesion molecule-1 (ICAM-1) in ECV 304 human endothelial cells. In addition, expression of two pro-inflammatory cytokines, TNF-alpha and interleukin-1 beta (IL-1 beta), was suppressed by Rg3. Reporter gene analyses revealed that minimal reporter activities of nuclear factor-kappa B (NF-kappa B) and activator protein-1 (AP-1) were blocked by Rg3 in a concentration-dependent manner. Taken together, these results indicate that Rg3 may have anti-inflammatory and anti-atherosclerotic activities in the vasculature, which is mediated partly by down-regulation of the expression of cell adhesion molecules and proinflammatory cytokines in endothelial cells.
引用
收藏
页码:699 / 701
页数:3
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