Semen Hoveniae extract protects against acute alcohol-induced liver injury in mice

被引:51
作者
Du, Jian [1 ]
He, Da [2 ]
Sun, Lian-Na [1 ]
Han, Ting [1 ]
Zhang, Hong [1 ]
Qin, Lu-Ping [1 ]
Rahman, Khalid [3 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Pharmacognosy, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Dept Pharmaceut Management, Shanghai 200433, Peoples R China
[3] Liverpool John Moores Univ, Fac Sci, Sch Biomol Sci, Liverpool L3 5UX, Merseyside, England
关键词
Semen Hoveniae; liver damage; gastric metabolism; INDUCED FATTY LIVER; LIPID-PEROXIDATION; ETHANOL-METABOLISM; OXIDATIVE STRESS; DULCIS THUNB; RATS; CIRRHOSIS; PATHOGENESIS; PROGRESSION; DISEASE;
D O I
10.3109/13880200903300196
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The protective effects of Semen Hoveniae extract (SHE) from Hovenia dulcis Thunb. (Rhamnaceae) on acute alcohol-induced liver injury were investigated in vivo using mice as test models. In the present study, SHE (150, 300, 600 mg/kg/day) was given to mice by intragastric administration for 4 days. Mice were gavaged with 60% ethanol 10 mL/kg after the last dose of extract. Six hours after alcohol administration, liver injury was evaluated by biochemical examination. Lipid peroxidation and the activity of antioxidants were measured by spectrophotometric methods. In mice, administration of SHE significantly decreased the activities of alanine aminotransferase (ALT) and aspartate transaminase (AST) in serum. Administration of SHE also protected against alcohol-induced alcohol dehydrogenase (ADH) elevation in mice. Concurrently, there was an augmentation in the activities of antioxidant enzymes such as superoxide dismutase (SOD), glutathione S-transferase (GST), and glutathione (GSH), and it also facilitated alcohol metabolism. Acute toxicity tests showed that a single dose of oral SHE up to 22 g/kg did not result in any death or toxic side effects in mice during 14 days' observation. These results demonstrate that SHE could protect against acute alcohol-induced liver injury without any toxic side effects. Therefore, Semen Hoveniae has potential for the development of a clinically useful agent which could protect the liver from alcohol-induced injury.
引用
收藏
页码:953 / 958
页数:6
相关论文
共 33 条
[1]   The role of liver alcohol dehydrogenase isoenzymes in the oxidation of glycolethers in male and female rats [J].
Aasmoe, L ;
Winberg, JO ;
Aarbakke, J .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 150 (01) :86-90
[2]  
[Anonymous], 1959, ARCH BIOCHEM BIOPHYS
[3]   Niuchangchih (Antrodia camphorata) and its potential in treating liver diseases [J].
Ao, Zong-Hua ;
Xu, Zheng-Hong ;
Lu, Zhen-Ming ;
Xu, Hong-Yu ;
Zhang, Xiao-Mei ;
Dou, Wen-Fang .
JOURNAL OF ETHNOPHARMACOLOGY, 2009, 121 (02) :194-212
[4]   Advances in alcoholic liver disease [J].
Arteel, G ;
Marsano, L ;
Mendez, C ;
Bentley, F ;
McClain, CJ .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2003, 17 (04) :625-647
[5]   Green tea extract protects against early alcohol-induced liver injury in rats [J].
Arteel, GE ;
Uesugi, T ;
Bevan, LN ;
Gäbele, E ;
Wheeler, MD ;
McKim, SE ;
Thurman, RG .
BIOLOGICAL CHEMISTRY, 2002, 383 (3-4) :663-670
[6]  
BERGMEYER HU, 1998, METHOD ENZYMAT AN, P261
[7]   Antioxidant capacity of flavanols and gallate esters: Pulse radiolysis studies [J].
Bors, W ;
Michel, C .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (11-12) :1413-1426
[8]  
Buege J A, 1978, Methods Enzymol, V52, P302
[9]   Introduction - Serial review: Alcohol, oxidative stress and cell injury [J].
Cederbaum, AI .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (12) :1524-1526
[10]   Alcohol and oxidative liver injury [J].
Dey, A ;
Cederbaum, AI .
HEPATOLOGY, 2006, 43 (02) :S63-S74