Influence of natural and synthetic compounds on cell surface expression of cell adhesion molecules, ICAM-1 and VCAM-1

被引:42
|
作者
Tanaka, S
Sakata, Y
Morimoto, K
Tambe, Y
Watanabe, Y
Honda, G
Tabata, M
Oshima, T
Masuda, T
Umezawa, T
Shimada, M
Nagakura, N
Kamisako, W
Kashiwada, Y
Ikeshiro, Y
机构
[1] Tokyo Univ Agr, Dept Biosci, Setagaya Ku, Tokyo 1568502, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Kyoto, Japan
[3] Kyoto Univ, Grad Sch Med, Kyoto, Japan
[4] Kyoto Univ, Inst Wood Sci, Uji, Kyoto, Japan
[5] Kobe Pharmaceut Univ, Higashinada Ku, Kobe, Hyogo 658, Japan
[6] Mukogawa Womens Univ, Nishinomiya, Hyogo, Japan
[7] Niigata Coll Pharm, Niigata 95021, Japan
关键词
Chalcone; cell adhesion molecule; ICAM-1; VCAM-1; immunosuppressive; anti-inflammatory;
D O I
10.1055/s-2001-11514
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Various natural and synthetic compounds including alkaloids, terpenoids and phenolics were tested for inhibition of the cell surface expression of intercellular adhesion molecule-1 (ICAM-1) and Vascular cell adhesion molecule-1 (VCAM-1), both of which are crucial in the regulation of immune response and inflammation. Of 40 compounds tested, two compounds significantly downregulated the expression of VCAM-1 on murine endothelial cells (F-2) and ten compounds that of ICAM-1 on mouse myeloid leukemia cells (M1). Sanguinarine chloride (5) and isoliquiritigenin (13) were capable of lowering the levels of both ICAM-1 and VCAM-1. The structure-activity relationships study on chalcone and flavone derivatives related to 13 suggested that the inhibitory activity of the chalcone derivatives is attributable to the 4-hydroxy group as well as the possible coplanarity between the phenyl ring and the adjacent conjugated ketone.
引用
收藏
页码:108 / 113
页数:6
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