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Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage

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...

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Detalles Bibliográficos
Autores principales: Schreiter, Thomas, Sowa, Jan-Peter, Schlattjan, Martin, Treckmann, Jürgen, Paul, Andreas, Strucksberg, Karl-Heinz, Baba, Hideo A., Odenthal, Margarete, Gieseler, Robert K., Gerken, Guido, Arteel, Gavin E., Canbay, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994032/
https://www.ncbi.nlm.nih.gov/pubmed/27550092
http://dx.doi.org/10.1038/srep31916
Descripción
Sumario: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.