Inhibitory effects of acylated kaempferol glycosides from the leaves of Cinnamomum kotoense on the proliferation of human peripheral blood mononuclear cells

被引:25
作者
Kuo, YC
Lu, CK
Huang, LW
Kuo, YH
Chang, C
Hsu, FL
Lee, TH [1 ]
机构
[1] Taipei Med Univ, Grad Inst Pharmacognosy Sci, Taipei 110, Taiwan
[2] Fu Jen Catholic Univ, Dept Life Sci, Taipei, Taiwan
[3] Natl Museum Marine Biol & Aquarium, Planning & Res Dept, Taipei, Taiwan
[4] Natl Taiwan Univ, Dept Chem, Taipei 10764, Taiwan
[5] Natl Museum Nat Sci, Dept Bot, Taichung, Taiwan
关键词
acylated kaempferol glycosides; Cinnamomum kotoense; Lauraceae; interleukin-2; leaves; PBMC proliferation;
D O I
10.1055/s-2005-864134
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A new chemical entity, namely kaempferol 3-O-alpha-L-[2-(Z)-p-coumaroyl-4-(E)-p-coumaroyl]rhamnopyranoside (1), and the known kaempferol 3-O-alpha-L-[2,4-di-(E)-p-coumaroyl]rhamnopyranoside (2) have been isolated from the methanolic extract of leaves of Cinnamomum kotoense. Structural elucidation of compounds 1 and 2 were achieved on the basis of spectroscopic analysis. The effects of compounds 1 and 2 on phytohemagglutinin (PHA) stimulated cell proliferation were studied towards human peripheral blood mononuclear cells (PBMC). The results indicated that compounds 1 and 2 suppressed PBMC proliferation induced by PHA with an IC50 value of 5.0 +/- 1.3 and 6.0 +/- 1.5 MM, respectively. Interleukin-2 production in activated PBMC inhibited by compounds 1 and 2 were in a concentration-dependent manner. Therefore, we suggested that compounds 1 and 2 in C. kotoense were likely the growth modulators for PBMC.
引用
收藏
页码:412 / 415
页数:4
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