Hau Desmond Kwok Po, Gambari Roberto, Wong Raymond Siu Ming, Yuen Marcus Chun Wah, Cheng Gregory Yin Ming, Tong Cindy Sze Wai, Zhu Guo Yuan, Leung Alexander Kai Man, Lai Paul Bo San, Lau Fung Yi, Chan Andrew Kit Wah, Wong Wai Yeung, Kok Stanton Hon Lung, Cheng Chor Hing, Kan Chi Wai, Chan Albert Sun Chi, Chui Chung Hin, Tang Johnny Cheuk On, Fong David Wang Fun
Research and Development Division, School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China.
Phytomedicine. 2009 Aug;16(8):751-60. doi: 10.1016/j.phymed.2009.01.008. Epub 2009 Apr 21.
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.
对乙酰氨基酚是治疗普通感冒和流感患者常用的药物。然而,过量服用对乙酰氨基酚可能会致命。在本研究中,我们调查了给小鼠腹腔注射致死剂量的对乙酰氨基酚后,再口服叶下珠提取物,是否可防止小鼠死亡。小鼠肝脏切片的组织病理学分析表明,叶下珠提取物可能保护肝细胞免受对乙酰氨基酚诱导的坏死。叶下珠提取物的治疗剂量对小鼠未显示出任何毒理学现象。用细胞色素P450 CYP2E1抗体进行免疫组织化学染色显示,叶下珠提取物降低了用致死剂量对乙酰氨基酚预处理的小鼠中细胞色素P450 CYP2E1蛋白水平。叶下珠提取物在体外也抑制细胞色素P450 CYP2E1酶活性。未发现砷、镉、汞和铅等重金属以及除草剂残留超过其检测限。高效液相色谱法鉴定出柯里拉京和没食子酸是叶下珠提取物的主要成分。我们得出结论,叶下珠提取物在减轻对乙酰氨基酚诱导的肝毒性方面是有效的,抑制细胞色素P450 CYP2E1酶可能是其治疗机制的一个重要因素。