(+)-Nootkatone and (+)-valencene from rhizomes of Cyperus rotundus increase survival rates in septic mice due to heme oxygenase-1 induction

被引:110
作者
Tsoyi, Konstantin [1 ]
Jang, Hwa Jin [1 ]
Lee, Young Soo [1 ]
Kim, Young Min [1 ]
Kim, Hye Jung [1 ]
Seo, Han Geuk [1 ]
Lee, Jae Heun [1 ]
Kwak, Jong Hwan [2 ]
Lee, Dong-Ung [3 ]
Chang, Ki Churl [1 ,4 ]
机构
[1] Gyeongsang Natl Univ, Inst Hlth Sci, Sch Med, Dept Pharmacol, Jinju 660290, South Korea
[2] Sungkyunkwan Univ, Coll Pharm, Suwon 440746, South Korea
[3] Dongguk Univ, Div Biosci, Gyeongju 780714, South Korea
[4] Gyeongsang Natl Univ, Res Inst Nat Sci, Jinju 660701, South Korea
关键词
Valencene; Nootkatone; Heme oxygenase-1; iNOS; Inflammation; Sepsis; GROUP BOX 1; NITRIC-OXIDE; RELEASE; INHIBITION; MONOXIDE; SEPSIS;
D O I
10.1016/j.jep.2011.07.062
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Ethnopharmacological relevance: The rhizomes of Cyperus rotundus have been used as traditional folk medicine for the treatment of inflammatory diseases. However, the mechanism by which extract of rhizomes of Cyperus rotundus (ECR) elicits anti-inflammation has not been extensively investigated so far. The aim of the present study was to test whether heme oxygenase (HO)-1 induction is involved in the anti-inflammatory action of ECR. Materials and methods: Induction of HO-1 and inhibition of inducible nitric oxide synthase (iNOS)/NO production by ECR and its 12 constituents (3 monoterpenes, 5 sesquiterpenes, and 4 aromatic compounds) were investigated using RAW264.7 cells in vitro. In addition, anti-inflammatory action of ECR and its two active ingredients (nookkatone, valencene) were confirmed in sepsis animal model in vivo. Results: ECR increased HO-1 expression in a concentration-dependent manner, which was correlated with significant inhibition of iNOS/NO production in LPS-activated RAW264.7 cells. Among 12 compounds isolated from ECR, mostly sesquiterpenes induced stronger HO-1 expression than monoterpenes in macrophage cells. Nootkatone and valencene (sesquiterpenes) significantly inhibited iNOS expression and NO production in LPS-simulated RAW264.7 cells. Inhibition of iNOS expression by nootkatone, valencene, and ECR were significantly reduced in siHO-1 RNA transfected cells. Furthermore, all three showed marked inhibition of high mobility group box-1 (HMGB1) in LPS-activated macrophages and increased survival rates in cecal ligation and puncture (CLP)-induced sepsis in mice. Conclusions: Taken together, we concluded that possible anti-inflammatory mechanism of ECR is, at least, due to HO-1 induction, in which sesquiterpenes such as nootkatone and valencene play a crucial role. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1311 / 1317
页数:7
相关论文
共 21 条
[1]
Bani-Hani Mohamed G, 2006, Pharmacol Rep, V58 Suppl, P132
[2]
Carbon monoxide liberated from carbon monoxide-releasing molecule CORM-2 attenuates inflammation in the liver of septic mice [J].
Cepinskas, Gediminas ;
Katada, Kazuhiro ;
Bihari, Aurelia ;
Potter, Richard F. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2008, 294 (01) :G184-G191
[3]
GUPTA MB, 1971, INDIAN J MED RES, V59, P76
[4]
Howard J., 1995, PHYTOCHEMISTRY, V40, P1633
[5]
The role of IFN-α and nitric oxide in the release of HMGB1 by RAW 264.7 cells stimulated with polyinosinic-polycytidylic acid or lipopolysaccharide [J].
Jiang, Weiwen ;
Pisetsky, David S. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (05) :3337-3343
[6]
Prevention of the expression of inducible nitric oxide synthase by a novel positive inotropic agent, YS 49, in rat vascular smooth muscle and RAW 264.7 macrophages [J].
Kang, YJ ;
Koo, EB ;
Lee, YS ;
Yun-Choi, HS ;
Chang, KC .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (02) :357-364
[7]
Bacterial Endotoxin Induces the Release of High Mobility Group Box 1 via the IFN-β Signaling Pathway [J].
Kim, Ju-Hyun ;
Kim, Seon-Ju ;
Lee, Im-Soon ;
Lee, Myung-Shik ;
Uematsu, Satoshi ;
Akira, Shizuo ;
Oh, Kwon Ik .
JOURNAL OF IMMUNOLOGY, 2009, 182 (04) :2458-2466
[8]
Knoebl P, 2010, WIEN MED WOCHENSCHR, V160, P129, DOI 10.1007/s10354-009-0738-9
[9]
Platelets as immune mediators: Their role in host defense responses and sepsis [J].
Li, Zhenyu ;
Yang, Fanmuyi ;
Dunn, Steve ;
Gross, A. Kendall ;
Smyth, Susan S. .
THROMBOSIS RESEARCH, 2011, 127 (03) :184-188
[10]
Inhibition of acetylcholinesterase activity by monoterpenoids with a p-menthane skeleton [J].
Miyazawa, M ;
Watanabe, H ;
Kameoka, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (03) :677-679