The inhibitory effect of triterpenoid glycosides originating from Sanguisorba officinalis on tissue factor activity and the production of TNF-α

被引:27
作者
Cho, Jae Youl
Yoo, Eun Sook
Cha, Bae Cheon
Park, Hwa-Jin
Rhee, Man Hee
Han, Yong Nam
机构
[1] Kangwon Natl Univ, Sch Biotechnol & Bioengn, Chunchon 200701, Kangwon, South Korea
[2] Daewoong Pharm Co, Inst Biosci, Yongin, South Korea
[3] Jeju Natl Univ, Coll Med, Dept Pharmacol, Cheju, South Korea
[4] Sangji Univ, Dept Bioind & Technol, Wonju, South Korea
[5] Inje Univ, Coll Biomed Sci & Engn, Dept Biomed Lab Sci, Kimhae, South Korea
[6] Kyungpook Natl Univ, Coll Vet Med, Taegu, South Korea
[7] Seoul Natl Univ, Inst Nat Prod Res, Seoul 151, South Korea
关键词
Sanguisorba officinalis L; rosaceae; ziyu-glycosides; ZYM-201; tissue factor; TNF-alpha;
D O I
10.1055/s-2006-947257
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
We examined the inhibitory effects of novel triterpene glycoside compounds [ziyu-glycoside II (ZY-II) and its methyl ester (ZYM-201)], which originated from the roots of Sanguisorba officinalis L. (Rosaceae), on tissue factor (TF) activity and tumor necrosis factor (TNF)-alpha production. In in vitro TF activity tests, ZY-II but not ZYM-201 strongly blocked lung TF activity with an IC50 value of 0.46 MM. By contrast, only ZYM-201 dose-dependently inhibited in vivo TF activity with an ED50 value of 1.7 mg/kg, when orally administered. Furthermore, ZYM-201 diminished both in vitro and in vivo TNF-alpha production with IC50 or ED50 values of 69.4 mu M and 87.4 mg/kg, respectively. Therefore, these results suggest either that ZYM-201 may be developed as a potent inhibitor of both TF- and TNF-alpha-mediated diseases such as atherosclerosis and septic shock, or it may be a lead compound to be derivatized for further improvement of its curative efficacy.
引用
收藏
页码:1279 / 1284
页数:6
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