Hepatoprotective effects of eburicoic acid and dehydroeburicoic acid from Antrodia camphorata in a mouse model of acute hepatic injury

被引:78
|
作者
Huang, Guan-Jhong [1 ]
Deng, Jeng-Shyan [2 ]
Huang, Shyh-Shyun [3 ]
Lee, Chao-Ying [2 ]
Hou, Wen-Chi [4 ]
Wang, Sheng-Yang [5 ]
Sung, Ping-Jyun [6 ,7 ]
Kuo, Yueh-Hsiung [8 ]
机构
[1] China Med Univ, Coll Pharm, Dept Chinese Pharmaceut Sci & Chinese Med Resourc, Taichung 404, Taiwan
[2] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung 413, Taiwan
[3] China Med Univ, Coll Pharm, Sch Pharm, Taichung 404, Taiwan
[4] Taipei Med Univ, Grad Inst Pharmacognosy, Taipei, Taiwan
[5] Natl Chung Hsing Univ, Dept Forestry, Taichung 402, Taiwan
[6] Natl Museum Marine Biol & Aquarium, Pingtung 944, Taiwan
[7] Natl Dong Hwa Univ, Grad Inst Marine Biotechnol, Pingtung 944, Taiwan
[8] China Med Univ, Tsuzuki Inst Tradit Med, Taichung 404, Taiwan
关键词
Antrodia camphorata; Eburicoic acid; Dehydroeburicoic acid; Anti-inflammation; NO; TNF-alpha; TETRACHLORIDE-INDUCED HEPATOTOXICITY; IN-VITRO; ANTI-INFLAMMATION; FRUITING BODY; MECHANISM; SILYMARIN; DAMAGE;
D O I
10.1016/j.foodchem.2013.03.061
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The hepatoprotective effects of eburicoic acid (TR1) and dehydroeburicoic acid (TR2) from Antrodia camphorata (AC) against carbon tetrachloride (CCl4)-induced liver damage were investigated in mice. TR1 and TR2 was administered intraperitoneally (i.p.) for 7 days prior to the administration of CCl4. Pretreatment with TR1 and TR2 prevented the elevation of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and liver lipid peroxides in CCl4-treated mice. The activities of antioxidant enzymes [catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GPx)], nitric oxide (NO) production, and tumour necrosis factor-alpha (TNF-alpha) were decreased after the treatment with TR1 and TR2 in CCl4-treated mice. Western blotting revealed that TR1 and TR2 significantly decreased inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expressions and increased the expression of cytochrome P4502E1 (CYP2E1) in CCl4-treated mice. Therefore, we speculate that TR1 and TR2 protect the liver from CCl4-induced hepatic damage via antioxidant and anti-inflammatory mechanisms. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3020 / 3027
页数:8
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