Department for Gastroenterology and Hepatology, Center for Internal Medicine, University Hospital, University Duisburg-Essen, Essen, Germany.
Department of General, Visceral and Transplantation Surgery, University Hospital, University Duisburg-Essen, Essen, Germany.
Sci Rep. 2016 Aug 23;6:31916. doi: 10.1038/srep31916.
Reliable test systems to identify hepatotoxicity are essential to predict unexpected drug-related liver injury. Here we present a human ex-vivo liver model to investigate acetaminophen-induced liver injury. Human liver tissue was perfused over a 30 hour period with hourly sampling from the perfusate for measurement of general metabolism and clinical parameters. Liver function was assessed by clearance of indocyanine green (ICG) at 4, 20 and 28 hours. Six pieces of untreated human liver specimen maintained stable liver function over the entire perfusion period. Three liver sections incubated with low-dose acetaminophen revealed strong damage, with ICG half-lives significantly higher than in non-treated livers. In addition, the release of microRNA-122 was significantly higher in acetaminophen-treated than in non-treated livers. Thus, this model allows for investigation of hepatotoxicity in human liver tissue upon applying drug concentrations relevant in patients.
可靠的测试系统对于识别肝毒性至关重要,可用于预测意外的药物相关肝损伤。在此,我们介绍了一种用于研究对乙酰氨基酚诱导肝损伤的人离体肝脏模型。用人肝组织进行 30 小时的灌流,每小时从灌流液中取样,用于测量一般代谢和临床参数。通过在 4、20 和 28 小时时测量吲哚菁绿(ICG)的清除率来评估肝功能。6 个人体肝标本在整个灌流期间保持稳定的肝功能。三块用低剂量对乙酰氨基酚孵育的肝切片显示出强烈的损伤,ICG 半衰期明显高于未经处理的肝脏。此外,在接受对乙酰氨基酚治疗的肝脏中,miRNA-122 的释放明显高于未经治疗的肝脏。因此,该模型允许在应用与患者相关的药物浓度时,在人肝组织中研究肝毒性。