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478715 
Journal Article 
Phyllanthus urinaria extract attenuates acetaminophen induced hepatotoxicity: Involvement of cytochrome P450 CYP2E1 
Hau, DKP; Gambari, R; Wong, RSM; Yuen, MCW; Cheng, GYM; Tong, CSW; Zhu, GY; Leung, AKM; Lai, PBS; Lau, FY; Chan, AKW; Wong, WY; Kok, SHL; Cheng, CH; Kan, CW; Chan, ASC; Chui, CH; Tang, JCO; Fong, DWF 
2009 
Phytomedicine
ISSN: 0944-7113
EISSN: 1618-095X 
16 
751-760 
English 
Acetaminophen is a commonly used drug for the treatment of patients with common cold and influenza. However, an overdose of acetaminophen may be fatal. In this study we investigated whether mice, administered intraperitoneally with a lethal dose or acetaminophen, when followed by oral administration of Phyllanthus urinaria extract, may be prevented from death. Histopathological. analysis of mouse liver sections showed that Phyllanthus urinaria extract may protect the hepatocytes from acetaminophen-induced necrosis. Therapeutic dose of Phyllanthus urinaria extract did not show any toxicological phenomenon on mice. Immunohistochemical staining with the cytochrome P450 CYP2E1 antibody revealed that Phyllanthus urinaria extract reduced the cytochrome P450 CYP2E1 protein level in mice pre-treated with a lethal dose of acetaminophen. Phyllanthus urinaria extract also inhibited the cytochrome P450 CYP2E1 enzymatic activity in vitro. Heavy metals, including arsenic, cadmium, mercury and lead, as well as herbicide residues were not found above their detection limits. High performance liquid chromatography identified corilagin and gallic acid as the major components of the Phyllanthus urinaria extract. We conclude that Phyllanthus urinaria extract is effective in attenuating the acetaminophen induced hepatotoxicity, and inhibition of cytochrome P450 CYP2E1 enzyme may be an important factor for its therapeutic mechanism. (C) 2009 Elsevier GmbH. All rights reserved. 
Acetaminophen; Cytochrome 450 CYP2E1; Hepatoprotection; Hepatotoxicity; Phyllanthus urinaria; sinensis fruit extract; lewis-lung-carcinoma; acute-renal-failure; carbon-tetrachloride; protective role; liver-damage; apoptosis; cells; expression; ingestion 
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