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Metabolic profiling during ex vivo machine perfusion of the human liver

As donor organ shortages persist, functional machine perfusion is under investigation to improve preservation of the donor liver. The transplantation of donation after circulatory death (DCD) livers is limited by poor outcomes, but its application may be expanded by ex vivo repair and assessment of...

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Autores principales: Bruinsma, Bote G., Sridharan, Gautham V., Weeder, Pepijn D., Avruch, James H., Saeidi, Nima, Özer, Sinan, Geerts, Sharon, Porte, Robert J., Heger, Michal, van Gulik, Thomas M., Martins, Paulo N., Markmann, James F., Yeh, Heidi, Uygun, Korkut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776101/
https://www.ncbi.nlm.nih.gov/pubmed/26935866
http://dx.doi.org/10.1038/srep22415
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author Bruinsma, Bote G.
Sridharan, Gautham V.
Weeder, Pepijn D.
Avruch, James H.
Saeidi, Nima
Özer, Sinan
Geerts, Sharon
Porte, Robert J.
Heger, Michal
van Gulik, Thomas M.
Martins, Paulo N.
Markmann, James F.
Yeh, Heidi
Uygun, Korkut
author_facet Bruinsma, Bote G.
Sridharan, Gautham V.
Weeder, Pepijn D.
Avruch, James H.
Saeidi, Nima
Özer, Sinan
Geerts, Sharon
Porte, Robert J.
Heger, Michal
van Gulik, Thomas M.
Martins, Paulo N.
Markmann, James F.
Yeh, Heidi
Uygun, Korkut
author_sort Bruinsma, Bote G.
collection PubMed
description As donor organ shortages persist, functional machine perfusion is under investigation to improve preservation of the donor liver. The transplantation of donation after circulatory death (DCD) livers is limited by poor outcomes, but its application may be expanded by ex vivo repair and assessment of the organ before transplantation. Here we employed subnormothermic (21 °C) machine perfusion of discarded human livers combined with metabolomics to gain insight into metabolic recovery during machine perfusion. Improvements in energetic cofactors and redox shifts were observed, as well as reversal of ischemia-induced alterations in selected pathways, including lactate metabolism and increased TCA cycle intermediates. We next evaluated whether DCD livers with steatotic and severe ischemic injury could be discriminated from ‘transplantable’ DCD livers. Metabolomic profiling was able to cluster livers with similar metabolic patterns based on the degree of injury. Moreover, perfusion parameters combined with differences in metabolic factors suggest variable mechanisms that result in poor energy recovery in injured livers. We conclude that machine perfusion combined with metabolomics has significant potential as a clinical instrument for the assessment of preserved livers.
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spelling pubmed-47761012016-03-09 Metabolic profiling during ex vivo machine perfusion of the human liver Bruinsma, Bote G. Sridharan, Gautham V. Weeder, Pepijn D. Avruch, James H. Saeidi, Nima Özer, Sinan Geerts, Sharon Porte, Robert J. Heger, Michal van Gulik, Thomas M. Martins, Paulo N. Markmann, James F. Yeh, Heidi Uygun, Korkut Sci Rep Article As donor organ shortages persist, functional machine perfusion is under investigation to improve preservation of the donor liver. The transplantation of donation after circulatory death (DCD) livers is limited by poor outcomes, but its application may be expanded by ex vivo repair and assessment of the organ before transplantation. Here we employed subnormothermic (21 °C) machine perfusion of discarded human livers combined with metabolomics to gain insight into metabolic recovery during machine perfusion. Improvements in energetic cofactors and redox shifts were observed, as well as reversal of ischemia-induced alterations in selected pathways, including lactate metabolism and increased TCA cycle intermediates. We next evaluated whether DCD livers with steatotic and severe ischemic injury could be discriminated from ‘transplantable’ DCD livers. Metabolomic profiling was able to cluster livers with similar metabolic patterns based on the degree of injury. Moreover, perfusion parameters combined with differences in metabolic factors suggest variable mechanisms that result in poor energy recovery in injured livers. We conclude that machine perfusion combined with metabolomics has significant potential as a clinical instrument for the assessment of preserved livers. Nature Publishing Group 2016-03-03 /pmc/articles/PMC4776101/ /pubmed/26935866 http://dx.doi.org/10.1038/srep22415 Text en Copyright © 2016, Macmillan Publishers Limited 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
Bruinsma, Bote G.
Sridharan, Gautham V.
Weeder, Pepijn D.
Avruch, James H.
Saeidi, Nima
Özer, Sinan
Geerts, Sharon
Porte, Robert J.
Heger, Michal
van Gulik, Thomas M.
Martins, Paulo N.
Markmann, James F.
Yeh, Heidi
Uygun, Korkut
Metabolic profiling during ex vivo machine perfusion of the human liver
title Metabolic profiling during ex vivo machine perfusion of the human liver
title_full Metabolic profiling during ex vivo machine perfusion of the human liver
title_fullStr Metabolic profiling during ex vivo machine perfusion of the human liver
title_full_unstemmed Metabolic profiling during ex vivo machine perfusion of the human liver
title_short Metabolic profiling during ex vivo machine perfusion of the human liver
title_sort metabolic profiling during ex vivo machine perfusion of the human liver
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776101/
https://www.ncbi.nlm.nih.gov/pubmed/26935866
http://dx.doi.org/10.1038/srep22415
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