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Phyllanthus urinaria extract attenuates acetaminophen induced hepatotoxicity: Involvement of cytochrome P450 CYP2E1
Authors:Desmond Kwok Po Hau  Roberto Gambari  Raymond Siu Ming Wong  Marcus Chun Wah Yuen  Gregory Yin Ming Cheng  Cindy Sze Wai Tong  Guo Yuan Zhu  Alexander Kai Man Leung  Paul Bo San Lai  Fung Yi Lau  Andrew Kit Wah Chan  Wai Yeung Wong  Stanton Hon Lung Kok  Chor Hing Cheng  Chi Wai Kan  Albert Sun Chi Chan  Chung Hin Chui  Johnny Cheuk On Tang  David Wang Fun Fong
Affiliation:1. Research and Development Division, School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China;2. BioPharmaNet, Department of Biochemistry and Molecular Biology, The University of Ferrara, Ferrara, Italy;3. Department of Medicine and Therapeutics, Li Ka Shing Medical Sciences Building, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China;4. Institute of Textiles and Clothing and Applied Biology, The Hong Kong Polytechnic University, Hong Kong, China;5. Department of Surgery, Li Ka Shing Medical Sciences Building, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China;6. Department of Chemistry, Hong Kong Baptist University, Hong Kong, China
Abstract: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 of 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.
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