Hepatoprotective Effect of Pinoresinol on Carbon Tetrachloride-Induced Hepatic Damage in Mice

被引:112
作者
Kim, Hyo-Yeon [1 ]
Kim, Joon-Ki [1 ]
Choi, Jun-Ho [1 ]
Jung, Joo-Yeon [1 ]
Oh, Woo-Yong [1 ]
Kim, Dong Chun [3 ]
Lee, Hee Sang [3 ]
Kim, Yeong Shik [2 ]
Kang, Sam Sik [2 ]
Lee, Seung-Ho [3 ]
Lee, Sun-Mee [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Suwon 440746, South Korea
[2] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[3] Yeungnam Univ, Coll Pharm, Kyongsan 712749, South Korea
关键词
carbon tetrachloride; hepatoprotective activity; inflammation; oxidative stress; pinoresinol; ACUTE LIVER-INJURY; NITRIC-OXIDE; FORSYTHIA-KOREANA; MEDICINAL-PLANTS; C-JUN; ROLES; GLUTATHIONE; ACTIVATION; MECHANISM; PROTECTS;
D O I
10.1254/jphs.09234FP
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Forsythiae Fructus is known to have diuretic, anti-bacterial, and anti-inflammatory activities. This study examined the hepatoprotective effects of pinoresinol, a lignan isolated from Forsythiae Fructus, against carbon tetrachloride (CCl4)-induced liver injury. Mice were treated intraperitoneally with vehicle or pinoresinol (25, 50, 100, and 200 mg/kg) 30 min before and 2 h after CCl4 (20 mu l/kg) injection. In the vehicle-treated CCl4 group, serum aminotransferase activities were significantly increased 24 h after CCl4 injection, and these increases were attenuated by pinoresinol at all doses. Hepatic glutathione contents were significantly decreased and lipid peroxidation was increased after CCl4 treatment. These changes were attenuated by 50 and 100 mg/kg of pinoresinol. The levels of protein and mRNA expression of inflammatory mediators, including tumor necrosis factor-alpha, inducible nitric oxide synthase, and cyclooxygenase-2, were significantly increased after CCl4 injection; and these increases were attenuated by pinoresinol. Nuclear translocation of nuclear factor-kappa B (NF-kappa B) and phosphorylation of c-Jun, one of the components of activating protein 1 (AP-1), were inhibited by pinoresinol. Our results suggest that pinoresinol ameliorates CCl4-induced acute liver injury, and this protection is likely due to anti-oxidative activity and down-regulation of inflammatory mediators through inhibition of NF-kappa B and AP-1.
引用
收藏
页码:105 / 112
页数:8
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