Triterpenoid saponin, oleanolic acid 3-O-β-D-glucopyranosyl(1→3)-α-L-rhamnopyranosyl(1→2)-α-L-arabinopyranoside (OA) from Aralia elata inhibits LPS-induced nitric oxide production by down-regulated NF-κB in raw 264.7 cells

被引:46
作者
Suh, Seok-Jong
Jin, Un-Ho
Kim, Kyung-Woon
Son, Jong-Keun
Lee, Seung Ho
Son, Kun-Ho
Chang, Hyen Wook
Lee, Young-Choon
Kim, Cheorl-Ho
机构
[1] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, South Korea
[2] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
[3] Andong Natl Univ, Dept Food & Nutr, Andong 760749, South Korea
[4] Dong A Univ, Dept Biotechnol, Pusan 608714, South Korea
关键词
inducible NO-synthase (iNOS); cyclooxygenase 2 (COX-2); NF-kappa; 13; extracellular signal regulated kinase 1 and 2 (ERK 1/2); c-Jun N-terminal; kinase (JNK); Raw; 264.7;
D O I
10.1016/j.abb.2007.08.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is well known that the pro-inflammatory mediators such as nitric oxide (NO) and prostaglandin (PG)E-2 are involved in several inflammatory diseases and lipopolysaccharide (LPS) can stimulate these inflammatory responses. Oleanolic acid 3-O-beta-D-glucopyranosyl(1 --> 3)-alpha-L-rhamnopyranosyl(1 --> 2)-alpha-L-arabinopyranoside (OA) was purified from edible plant Aralia elata. OA inhibited LPS-induced NO and PGE(2) production in raw 264.7 murine macrophages in a dose-dependent manner and RT-PCR analysis indicated OA inhibited mRNA transcriptions of iNOS and COX-2 genes in LPS-induced cells. EMSA and Western blot analysis revealed that OA drastically reduced NF-kappa B translocation by the inhibition effects of LPS-induced phosphorylation of I kappa B alpha. In addition, it was found that OA inhibited the phosphorylation of ERK1/2, p38 and JNK MAPK, and the treatment of U0126 in LPS-induced raw 264.7 cells showed significant inhibition activity on the NO production and the phosphorylation of I kappa B alpha. Taken together, it is suggested that OA from A. elata has an anti-inflammatory activity via down-regulation of NF-kappa B. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 233
页数:7
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