Hepatoprotective activity of Chhit-Chan-Than extract powder against carbon tetrachloride-induced liver injury in rats

被引:33
作者
Lin, Yi-Chun [1 ]
Cheng, Kuei-Mei [2 ]
Huang, Hsin-Yu [3 ,4 ]
Chao, Pei-Yu [5 ,6 ]
Hwang, Jin-Ming [7 ]
Lee, Hsueh-Hui [8 ,9 ]
Lu, Cheng-You [10 ]
Chiu, Yung-Wei [1 ,10 ]
Liu, Jer-Yuh [11 ,12 ]
机构
[1] Tungs Taichung MetroHarbor Hosp, Emergency Dept, Taichung, Taiwan
[2] Natl Taiwan Univ Phys Educ & Sport, Dept Sports Management, Taichung, Taiwan
[3] Natl Chung Hsing Univ, Dept Food Sci & Biotechnol, Taichung 40227, Taiwan
[4] Wu Feng Univ, Dept Hospitality Management, Chiayi, Taiwan
[5] Natl Chin Yi Univ Technol, Dept Leisure Ind Management, Taichung, Taiwan
[6] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[7] Chung Shan Med Univ, Sch Appl Chem, Hlth Care & Management Coll, Taichung, Taiwan
[8] Chung Shan Med Univ, Inst Biochem & Biotechnol, Taichung, Taiwan
[9] Kuang Tien Gen Hosp, Dept Clin Lab, Taichung, Taiwan
[10] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[11] China Med Univ Hosp, Ctr Mol Med, Taichung, Taiwan
[12] China Med Univ, Grad Inst Canc Biol, Taichung, Taiwan
关键词
Antioxidants; Carbon tetrachloride; Hepatoprotection; OCIMUM-GRATISSIMUM; ANTIOXIDANT PROPERTIES; MOLECULAR-MECHANISMS; LIPID-PEROXIDATION; HEPATIC-FIBROSIS; OXIDATIVE DAMAGE; SILYMARIN; ACID; TOXICITY; METABOLISM;
D O I
10.1016/j.jfda.2013.09.012
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The capability of Chhit-Chan-Than extract powder (CCTEP, 10% aqueous Ocimum gratissimum L. extract) to protect against carbon tetrachloride (CCl4)-induced oxidative stress and hepatotoxicity in vivo was investigated. Wistar rats were divided into five groups. Group A was a normal control group given only vehicle; Group B, the hepatotoxic group, was injected intraperitoneally twice a week with repeated 8% CCl4/olive oil (0.1 mL/100 g of body weight); Groups C-E, extract-treated groups received CCl4 and different doses of CCTEP (100 mg/kg and 200 mg/kg) or silymarin (200 mg/kg of body weight) daily by gavage for 8 weeks, respectively. The results showed that the CCl4-induced histopathogical changes may be prevented by CCTEP through reducing the intercellular collogen stack, dropping blood serum alanine aminotransferase and aspartate aminotransferase levels, and restoring the catalase activity and glutathione content. The hepatoprotective properties were further confirmed by the marked improvement in histopathological examination and by quantitative steatosis-fibrosis scoring. The above results suggest that CCTEP is able to prevent the liver inflammation and fibrosis induced by repeated CCl4, administration, and the hepatoprotective effects might be correlated partly with its antioxidant and free radical scavenging effects. Copyright (C) 2013, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC. All rights reserved.
引用
收藏
页码:220 / 229
页数:10
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