Hepatoprotective effects of polymethoxyflavones against acute and chronic carbon tetrachloride intoxication

被引:28
作者
Kim, Tae-Won [1 ,2 ]
Lee, Dong-Ryung [3 ]
Choi, Bong-Keun [3 ]
Kang, Hwan-Kyu [1 ,2 ]
Jung, Ju-Young [1 ,2 ]
Lim, Seol-Wa [4 ]
Yang, Seung Hwan [5 ]
Suh, Joo-Won [5 ]
机构
[1] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[2] Chungnam Natl Univ, Inst Vet Sci, Taejon 305764, South Korea
[3] NutraPham Tech, Yongin 449728, Gyeonggi, South Korea
[4] Catholic Univ, Grad Sch Biomed & Hlth Sci, Seoul 06591, South Korea
[5] Myongji Univ, Ctr Nutraceut & Pharmaceut Mat, Yongin 449728, Gyeonggi, South Korea
关键词
Citrus aurantium extract (CAE); Carbon tetrachloride (CCl4); Liver damage; Acute model; Chronic model; NF-KAPPA-B; INDUCED LIVER-INJURY; INDUCED HEPATOTOXICITY; LIPID-PEROXIDATION; HEPATIC-FIBROSIS; OXIDATIVE STRESS; CITRUS FLAVONOIDS; GENE-EXPRESSION; MOUSE MODEL; EXTRACT;
D O I
10.1016/j.fct.2016.03.004
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In the present study, we explore the protective effects of Citrus aurantium L. extract (CAE) against acute and chronic CCl4-induced hepatotoxicity. The quantitative analysis of CAE was performed using HPLC-UV to determine the nobiletin content was approximately 27%. For the acute model, the male ICR mice were orally treated with water, silymarin (positive control, 200 mg/kg) and CAE (50 and 200 mg/kg) for 3 days prior to CCl4 (1 mL/kg, 50% v/v in olive oil) IP injection. For the chronic model (n = 6/group), the mice were treated with each treatment for 28 consecutive days and CCl4 (1 mL/kg, 20%) was injected twice a week. In both the acute and chronic models, the CCl4 alone treated group showed histopathologic alterations with a significantly increase in serum hepatic enzyme levels together with a disrupted anti oxidative status. In contrast, the CAE treatments restored pathologic alterations and recovered the oxidative status by enhancing antioxidant enzymes and reducing lipid peroxidation levels. Furthermore, CAE enhanced nuclear factor E2-related factor 2 (Nrf2) and its related cytoprotective signals, including NAD(P)H quinone oxidoreductase 1, UDP-glucuronosyltransferase, and gamma-glutamylcysteine synthetase. Taken together, the present study demonstrates that CAE exerts a protective effect against CCl4-induced hepatotoxicity with its anti-oxidant, anti-inflammatory, and anti-apoptotic activity. (C) 2016 Published by Elsevier Ltd.
引用
收藏
页码:91 / 99
页数:9
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