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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4994032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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