Polyphenols Extracted from Hibiscus sabdariffa L. Inhibited Lipopolysaccharide-Induced Inflammation by Improving Antioxidative Conditions and Regulating Cyclooxygenase-2 Expression

被引:70
作者
Kao, Erl-Shyh [3 ]
Hsu, Jeng-Dong [2 ]
Wang, Chau-Jong [1 ]
Yang, Su-Huei [1 ]
Cheng, Su-Ya [4 ]
Lee, Huei-Jane [1 ]
机构
[1] Chung Shan Med Univ, Coll Med, Inst Biochem & Biotechnol, Taichung 402, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Pathol, Taichung 402, Taiwan
[3] Chien Kuo Technol Univ, Coll Humanity, Dept Beauty Sci, Changhua 500, Taiwan
[4] Chung Shan Med Univ Hosp, Clin Lab, Taichung 402, Taiwan
关键词
anti-inflammation; Hibiscus sabdariffa L; lipopolysaccharide; macrophage; Malvaceae; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; OXIDATIVE STRESS; DOWN-REGULATION; MACROPHAGES; APOPTOSIS; CELLS; PHOSPHORYLATION; SUPPRESSION; ACTIVATION;
D O I
10.1271/bbb.80639
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
Oxidative stress and inflammation are related to several chronic diseases including cancer and atherosclerosis. Hibiscus sabdariffa Linnaeus has been found to possess antioxidant effects. In this study, polyphenols extracted from Hibiscus sabdariffa L. (HPE) were used to detect anti-inflammatory effects on nitrite and prostaglandin E-2 (PGE(2)) in. lipopolysaccharide (LPS) treated RAW264.7 cells. Sequentially, an animal model examination was performed to confirm the effects of HPE on LPS-induced hepatic inflammation. The results showed that HPE reduced 94.6% of xanthine oxidase activity in vitro, and decreased nitrite and PGE2 secretions in LPS-induced cells. In LPS-treated rats, HPE significantly decreased the serum levels of alanine and aspartate aminotransferase. In the liver, lipid peroxidation and liver lesions decreased, and catalase activity and glutathione increased. The study also revealed that down-regulation of cyclooxygenase-2 (COX-2), p-c-Jun N-terminal kinase (p-JNK) and p-P38 might have been involved. In sum, this study found an anti-inflammatory potency of HPE both in vitro and in vivo.
引用
收藏
页码:385 / 390
页数:6
相关论文
共 27 条
[1]  
Aebi H., 1974, Methods of Enzymatic Analysis, P673, DOI DOI 10.1016/B978-0-12-091302-2.50032-3
[2]   Nuclear factor-κ-B:: The enemy within [J].
Aggarwal, BB .
CANCER CELL, 2004, 6 (03) :203-208
[3]  
Barrios-Rodiles M, 1999, J IMMUNOL, V163, P963
[4]   CURCUMIN, AN ANTITUMOR PROMOTER AND ANTIINFLAMMATORY AGENT, INHIBITS INDUCTION OF NITRIC-OXIDE SYNTHASE IN ACTIVATED MACROPHAGES [J].
BROUET, I ;
OHSHIMA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 206 (02) :533-540
[5]   Hibiscus anthocyanins-rich extract inhibited LDL oxidation and oxLDL-mediated macrophages apoptosis [J].
Chang, Yun-Ching ;
Huang, Kai-Xun ;
Huang, An-Chung ;
Ho, Yung-Chyuan ;
Wang, Chau-Jong .
FOOD AND CHEMICAL TOXICOLOGY, 2006, 44 (07) :1015-1023
[6]   Hibiscus sabdariffa extract inhibits the development of atherosclerosis in cholesterol-fed rabbits [J].
Chen, CC ;
Hsu, JD ;
Wang, SF ;
Chiang, HC ;
Yang, MY ;
Kao, ES ;
Ho, YC ;
Wang, CJ .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (18) :5472-5477
[7]   RENAL ABNORMALITIES AND AN ALTERED INFLAMMATORY RESPONSE IN MICE LACKING CYCLOOXYGENASE-II [J].
DINCHUK, JE ;
CAR, BD ;
FOCHT, RJ ;
JOHNSTON, JJ ;
JAFFEE, BD ;
COVINGTON, MB ;
CONTEL, NR ;
ENG, VM ;
COLLINS, RJ ;
CZERNIAK, PM ;
GORRY, SA ;
TRZASKOS, JM .
NATURE, 1995, 378 (6555) :406-409
[8]  
Duval DL, 1996, MOL PHARMACOL, V50, P277
[9]   PROSTAGLANDIN-H SYNTHASE AND XENOBIOTIC OXIDATION [J].
ELING, TE ;
THOMPSON, DC ;
FOUREMAN, GL ;
CURTIS, JF ;
HUGHES, MF .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1990, 30 :1-45
[10]  
Good PF, 1996, AM J PATHOL, V149, P21