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A rat model of dual-flow liver machine perfusion system

PURPOSE: As clinical liver perfusion systems use portal vein and artery flow, dual perfusion techniques are required even in small animal models in order to reproduce clinical setting. The aim of this study was to construct a new dual-flow perfusion system in rat model and optimized the oxygen suppl...

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Autores principales: Ohara, Masayuki, Ishikawa, Jun, Yoshimoto, Syuhei, Hakamata, Yoji, Kobayashi, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664844/
https://www.ncbi.nlm.nih.gov/pubmed/37909599
http://dx.doi.org/10.1590/acb387723
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author Ohara, Masayuki
Ishikawa, Jun
Yoshimoto, Syuhei
Hakamata, Yoji
Kobayashi, Eiji
author_facet Ohara, Masayuki
Ishikawa, Jun
Yoshimoto, Syuhei
Hakamata, Yoji
Kobayashi, Eiji
author_sort Ohara, Masayuki
collection PubMed
description PURPOSE: As clinical liver perfusion systems use portal vein and artery flow, dual perfusion techniques are required even in small animal models in order to reproduce clinical setting. The aim of this study was to construct a new dual-flow perfusion system in rat model and optimized the oxygen supply to ensure the aerobic metabolization. METHODS: The dual-flow circuit was fabricated using rat liver and whole blood samples as perfusates. The oxygen supply was controlled according to the amount of dissolved oxygen in the perfusate. Perfusate parameters and adenosine triphosphate (ATP) levels were analyzed to evaluate organ function and metabolic energy state. Stored whole blood also tested the suitability as perfusate. RESULTS: Stored blood showed decrease oxygen delivery and liver function compared to fresh blood. Using fresh blood as perfusate with air only, the dissolved oxygen levels remained low and anaerobic metabolism increased. In contrast, with oxygen control at living body level, anaerobic metabolism was well suppressed, and tissue ATP content was increased. CONCLUSIONS: We developed a new dual-flow system that enable to reproduce the clinical settings. The perfusion system showed the possibility to improve the energy metabolic state of the perfused organ under appropriate partial pressure of oxygen.
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spelling pubmed-106648442023-10-30 A rat model of dual-flow liver machine perfusion system Ohara, Masayuki Ishikawa, Jun Yoshimoto, Syuhei Hakamata, Yoji Kobayashi, Eiji Acta Cir Bras Original Article PURPOSE: As clinical liver perfusion systems use portal vein and artery flow, dual perfusion techniques are required even in small animal models in order to reproduce clinical setting. The aim of this study was to construct a new dual-flow perfusion system in rat model and optimized the oxygen supply to ensure the aerobic metabolization. METHODS: The dual-flow circuit was fabricated using rat liver and whole blood samples as perfusates. The oxygen supply was controlled according to the amount of dissolved oxygen in the perfusate. Perfusate parameters and adenosine triphosphate (ATP) levels were analyzed to evaluate organ function and metabolic energy state. Stored whole blood also tested the suitability as perfusate. RESULTS: Stored blood showed decrease oxygen delivery and liver function compared to fresh blood. Using fresh blood as perfusate with air only, the dissolved oxygen levels remained low and anaerobic metabolism increased. In contrast, with oxygen control at living body level, anaerobic metabolism was well suppressed, and tissue ATP content was increased. CONCLUSIONS: We developed a new dual-flow system that enable to reproduce the clinical settings. The perfusion system showed the possibility to improve the energy metabolic state of the perfused organ under appropriate partial pressure of oxygen. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2023-10-30 /pmc/articles/PMC10664844/ /pubmed/37909599 http://dx.doi.org/10.1590/acb387723 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ohara, Masayuki
Ishikawa, Jun
Yoshimoto, Syuhei
Hakamata, Yoji
Kobayashi, Eiji
A rat model of dual-flow liver machine perfusion system
title A rat model of dual-flow liver machine perfusion system
title_full A rat model of dual-flow liver machine perfusion system
title_fullStr A rat model of dual-flow liver machine perfusion system
title_full_unstemmed A rat model of dual-flow liver machine perfusion system
title_short A rat model of dual-flow liver machine perfusion system
title_sort rat model of dual-flow liver machine perfusion system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664844/
https://www.ncbi.nlm.nih.gov/pubmed/37909599
http://dx.doi.org/10.1590/acb387723
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