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Effect of a fennented ginseng extract, BST204, on the expression of cyclooxygenase-2 in murine macrophages
被引:33
|作者:
Seo, JY
Lee, JH
Kim, NW
Her, E
Chang, SH
Ko, NY
Yoo, YH
Kim, JW
Seo, DW
Han, JW
Kim, YM
Choi, WS
[1
]
机构:
[1] Konkuk Univ, Dept Immunol, Coll Med, Chungju 380701, South Korea
[2] Biosapogen, Gyeonggi Do 462120, South Korea
[3] NCI, Pathol Lab, NIH, Rockville, MD 20852 USA
[4] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
[5] Duksung Womens Univ, Coll Pharm, Seoul 132714, South Korea
关键词:
COX-2;
PGE(2);
BST204;
fermented ginseng extract;
p70;
S6;
kinase;
D O I:
10.1016/j.intimp.2005.01.008
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
This paper investigates how BST204, a fermented ginseng extract, affects the expression and mechanism of cyclooxygenase-2 (COX-2). BST204 was prepared by incubating crude ginseng extract with ginsenoside-beta-glucosidase. Unexpectedly, BST204 had no effect on the level of COX-2 protein in unstimulated RAW 264.7 cells, and it suppressed the level of COX-2 protein and PGE(2) production in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. It did not show any suppressive effect, though, on the COX-2 mRNA level. To investigate the suppressive mechanism of COX-2 protein, the activating phosphorylation of p70 S6 kinase and 4E-BP1, which are important for translation, were measured. The phosphorylation of p70 S6 kinase, not 4E-BP1, was increased by LPS in a time-dependent manner, and was inhibited by BST204 in a dose-dependent manner. The expression of COX-2 protein, however, was partially suppressed by rapamycin, an upstream inhibitor of p70 S6 kinase. Therefore, this paper suggests that the suppression of COX-2 protein by BST204 was partially correlated with the inhibition of p70 S6 kinase activation. (c) 2005 Elsevier B.V. All rights reserved.
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页码:929 / 936
页数:8
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