Anti-inflammatory effects of schisandrin isolated from the fruit of Schisandra chinensis Baill

被引:200
作者
Guo, Lian Yu [1 ]
Hung, Tran Manh [2 ]
Bae, Ki Hwan [2 ]
Shin, Eun Myoung [1 ]
Zhou, Hong Yu [1 ]
Hong, Yoo Na [1 ]
Kang, Sam Sik [1 ]
Kim, Hyun Pyo [3 ]
Kim, Yeong Shik [1 ]
机构
[1] Seoul Natl Univ, Inst Nat Prod Res, Coll Pharm, Seoul 151742, South Korea
[2] Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea
[3] Kangwon Natl Univ, Coll Pharm, Chunchon 200701, South Korea
关键词
schisandrin; inducible nitric oxide synthase; cyclooxygenase-2; nuclear factor-kappaB; c-Jun N-terminal kinase; p38 mitogen-activated protein kinase; paw edema; vascular permeability; septic shock;
D O I
10.1016/j.ejphar.2008.06.074
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Schisandrin is the main active ingredient isolated from the fruit of Schisandra chinensis Baill. Recent studies have demonstrated that schisandrin exhibits anti-oxidative effects in vivo. In the present study, the effect of schisandrin on plasma nitrite concentration in lipopolysaccharide (LPS)-treated mice was evaluated. It also significantly inhibited carrageenan-induced paw edema and acetic acid-induced vascular permeability in mice. Furthermore, schisandrin had a protective effect on lipopolysaccharide (LPS)-induced sepsis. In vitro, our results are the first that show that the anti-inflammatory properties of schisandrin result from the inhibition of nitric oxide (NO) production, prostaglandin E-2 (PGE(2)) release, cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, which in turn results from the inhibition of nuclear factor-kappaB (NF-kappa B), c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) activities in a RAW 264.7 macrophage cell line. (c) 2008 Published by Elsevier B.V.
引用
收藏
页码:293 / 299
页数:7
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