Cargando…
A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus
A feasible large animal model to evaluate regenerative medicine techniques is vital for developing clinical applications. One such appropriate model could be to use retrorsine (RS) together with partial hepatectomy (PH). Here, we have developed the first porcine model using RS and PH. RS or saline c...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177392/ https://www.ncbi.nlm.nih.gov/pubmed/30301901 http://dx.doi.org/10.1038/s41598-018-32889-y |
_version_ | 1783361846483353600 |
---|---|
author | Inomata, Kenta Tajima, Kazuki Yagi, Hiroshi Higashi, Hisanobu Shimoda, Hirofumi Matsubara, Kentaro Hibi, Taizo Abe, Yuta Tsujikawa, Hanako Kitago, Minoru Shinoda, Masahiro Obara, Hideaki Itano, Osamu Soto-Gutierrez, Alejandro Kitagawa, Yuko |
author_facet | Inomata, Kenta Tajima, Kazuki Yagi, Hiroshi Higashi, Hisanobu Shimoda, Hirofumi Matsubara, Kentaro Hibi, Taizo Abe, Yuta Tsujikawa, Hanako Kitago, Minoru Shinoda, Masahiro Obara, Hideaki Itano, Osamu Soto-Gutierrez, Alejandro Kitagawa, Yuko |
author_sort | Inomata, Kenta |
collection | PubMed |
description | A feasible large animal model to evaluate regenerative medicine techniques is vital for developing clinical applications. One such appropriate model could be to use retrorsine (RS) together with partial hepatectomy (PH). Here, we have developed the first porcine model using RS and PH. RS or saline control was administered intraperitoneally to Göttingen miniature pigs twice, two weeks apart. Four weeks after the second dose, animals underwent PH. Initially, we tested different doses of RS and resection of different amounts of liver, and selected 50 mg/kg RS with 60% hepatectomy as our model for further testing. Treated animals were sacrificed 3, 10, 17 or 28 days after PH. Blood samples and resected liver were collected. Serum and liver RS content was determined by Liquid Chromatograph-tandem Mass Spectrometer. Blood analyses demonstrated liver dysfunction after PH. Liver regeneration was significantly inhibited 10 and 17 days after PH in RS-treated animals, to the extent of 20%. Histological examination indicated hepatic injury and regenerative responses after PH. Immunohistochemical staining demonstrated accumulation of Cyclin D1 and suppression of Ki-67 and PCNA in RS-treated animals. We report the development of the first large animal model of sustained liver injury with suppression of hepatic regeneration. |
format | Online Article Text |
id | pubmed-6177392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61773922018-10-12 A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus Inomata, Kenta Tajima, Kazuki Yagi, Hiroshi Higashi, Hisanobu Shimoda, Hirofumi Matsubara, Kentaro Hibi, Taizo Abe, Yuta Tsujikawa, Hanako Kitago, Minoru Shinoda, Masahiro Obara, Hideaki Itano, Osamu Soto-Gutierrez, Alejandro Kitagawa, Yuko Sci Rep Article A feasible large animal model to evaluate regenerative medicine techniques is vital for developing clinical applications. One such appropriate model could be to use retrorsine (RS) together with partial hepatectomy (PH). Here, we have developed the first porcine model using RS and PH. RS or saline control was administered intraperitoneally to Göttingen miniature pigs twice, two weeks apart. Four weeks after the second dose, animals underwent PH. Initially, we tested different doses of RS and resection of different amounts of liver, and selected 50 mg/kg RS with 60% hepatectomy as our model for further testing. Treated animals were sacrificed 3, 10, 17 or 28 days after PH. Blood samples and resected liver were collected. Serum and liver RS content was determined by Liquid Chromatograph-tandem Mass Spectrometer. Blood analyses demonstrated liver dysfunction after PH. Liver regeneration was significantly inhibited 10 and 17 days after PH in RS-treated animals, to the extent of 20%. Histological examination indicated hepatic injury and regenerative responses after PH. Immunohistochemical staining demonstrated accumulation of Cyclin D1 and suppression of Ki-67 and PCNA in RS-treated animals. We report the development of the first large animal model of sustained liver injury with suppression of hepatic regeneration. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177392/ /pubmed/30301901 http://dx.doi.org/10.1038/s41598-018-32889-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Inomata, Kenta Tajima, Kazuki Yagi, Hiroshi Higashi, Hisanobu Shimoda, Hirofumi Matsubara, Kentaro Hibi, Taizo Abe, Yuta Tsujikawa, Hanako Kitago, Minoru Shinoda, Masahiro Obara, Hideaki Itano, Osamu Soto-Gutierrez, Alejandro Kitagawa, Yuko A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title | A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title_full | A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title_fullStr | A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title_full_unstemmed | A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title_short | A Pre-Clinical Large Animal Model of Sustained Liver Injury and Regeneration Stimulus |
title_sort | pre-clinical large animal model of sustained liver injury and regeneration stimulus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177392/ https://www.ncbi.nlm.nih.gov/pubmed/30301901 http://dx.doi.org/10.1038/s41598-018-32889-y |
work_keys_str_mv | AT inomatakenta apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT tajimakazuki apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT yagihiroshi apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT higashihisanobu apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT shimodahirofumi apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT matsubarakentaro apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT hibitaizo apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT abeyuta apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT tsujikawahanako apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT kitagominoru apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT shinodamasahiro apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT obarahideaki apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT itanoosamu apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT sotogutierrezalejandro apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT kitagawayuko apreclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT inomatakenta preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT tajimakazuki preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT yagihiroshi preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT higashihisanobu preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT shimodahirofumi preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT matsubarakentaro preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT hibitaizo preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT abeyuta preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT tsujikawahanako preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT kitagominoru preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT shinodamasahiro preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT obarahideaki preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT itanoosamu preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT sotogutierrezalejandro preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus AT kitagawayuko preclinicallargeanimalmodelofsustainedliverinjuryandregenerationstimulus |