A curcuminoid and sesquiterpenes as inhibitors of macrophage TNF-α release from Curcuma zedoaria

被引:76
作者
Jang, MK
Sohn, DH
Ryu, JH
机构
[1] Sookmyung Womens Univ, Coll Pharm, Yongsan Ku, Seoul 140742, South Korea
[2] Wonkwang Univ, Coll Pharm, Iksan, Geonbuk, South Korea
[3] Wonkwang Univ, Med Resources Res Ctr, Iksan, Geonbuk, South Korea
关键词
D O I
10.1055/s-2001-16482
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Tumor necrosis factor-alpha (TNF-alpha) is one of the major mediators produced in activated macrophages which contribute to the circulatory failure associated with septic shock. in the course of screening marketed oriental anti-inflammatory herbal drugs for TNF-alpha antagonistic activity, a crude methanolic extract of the rhizomes of Curcuma zedoaria exhibited significant activity. The activity-guided fractionation and repetitive chromatographic procedures with the EtOAc-soluble fraction resulted in the isolation of three active compounds. They were identified as 1,7-bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one (1). procurcumenol (2) and epiprocurcumenol (3) by spectral data analysis. They inhibited the production of TNF-a by lipopolysaccharide (LPS)-activated macrophages from the results of bioassay (IC50 values of 1 and 2 are 12.3 and 310.5 muM, respectively) and Western blot assay. These results imply that the traditional use of C. zedoaria rhizome as anti-inflammatory drug may be explained at least in part, by the inhibition of TNF-alpha production.
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页码:550 / 552
页数:3
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