Studies on the protective effects of caffeic acid and quercetin on chemical-induced hepatotoxicity in rodents

被引:124
作者
Janbaz, KH
Saeed, SA
Gilani, AH [1 ]
机构
[1] Aga Khan Univ, Coll Med, Dept Biol & Biomed Sci, Karachi 74800, Pakistan
[2] Bahauddin Zakariya Univ, Fac Pharm, Multan, Pakistan
关键词
caffeic acid; quercetin; hepatoprotective; paracetaniol; CCl4; rodents;
D O I
10.1016/j.phymed.2003.05.002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Caffeic acid and quercetin, the well-known phenolic compounds widely present in the plant kingdom, were investigated for their possible protective effects against paracetamol and CCl4-induced hepatic damage. Paracetamol at the oral dose of 1 g/kg produced 100% mortality in mice while pretreatment of separate groups of animals with caffeic acid (6 mg/kg) and quercetin (10 mg/kg) reduced the death rate to 20% and 30%, respectively. Oral administration of sub-lethal dose of paracetamol (640 mg/kg) produced liver damage in rats as manifested by the significant (P < 0.01) rise in serum levels of aminotransferases (aspartate transaminase (AST) and alanine transaminase (ALT)) compared to respective control values. The serum enzyme values were significantly (P < 0.01) lowered on pretreatment of rats with either caffeic acid (6 mg/kg) or quercetin (10 mg/kg). Similarly, the hepatotoxic dose of CCl4 (1.5 ml/kg; orally) also raised significantly (P < 0.05) the serum AST and ALT levels as compared to control values. The same dose of the caffeic acid and quercetin was able to prevent CCl4-induced rise in serum enzymes. Caffeic acid and quercetin also prevented the CCl4-induced prolongation in pentobarbital sleeping time confirming their hepatoprotectivity. These results indicate that caffeic acid and quercetin exhibited hepatoprotective activity possibly through multiple mechanisms. (C) 2004 Elsevier GmbH. All rights reserved.
引用
收藏
页码:424 / 430
页数:7
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