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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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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
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author 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
author_facet 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
author_sort Schreiter, Thomas
collection PubMed
description 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.
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spelling pubmed-49940322016-08-30 Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage 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 Sci Rep Article 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. Nature Publishing Group 2016-08-23 /pmc/articles/PMC4994032/ /pubmed/27550092 http://dx.doi.org/10.1038/srep31916 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
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
Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title_full Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title_fullStr Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title_full_unstemmed Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title_short Human Ex-Vivo Liver Model for Acetaminophen-induced Liver Damage
title_sort human ex-vivo liver model for acetaminophen-induced liver damage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994032/
https://www.ncbi.nlm.nih.gov/pubmed/27550092
http://dx.doi.org/10.1038/srep31916
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