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Biochemical and morphological responses to post-hepatectomy liver failure in rats

The upper limit for partial hepatectomy (PH) in rats is 90%, which is associated with an increased risk of post-hepatectomy liver failure (PHLF), correlating with high mortality. Sixty-eight rats were randomized to 90% PH, sham operation, or no surgery. Further block randomization was performed to d...

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Autores principales: Lund, Andrea, Andersen, Kasper Jarlhelt, Meier, Michelle, Pedersen, Marie Ingemann, Knudsen, Anders Riegels, Kirkegård, Jakob, Mortensen, Frank Viborg, Nyengaard, Jens Randel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439910/
https://www.ncbi.nlm.nih.gov/pubmed/37598250
http://dx.doi.org/10.1038/s41598-023-40736-y
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author Lund, Andrea
Andersen, Kasper Jarlhelt
Meier, Michelle
Pedersen, Marie Ingemann
Knudsen, Anders Riegels
Kirkegård, Jakob
Mortensen, Frank Viborg
Nyengaard, Jens Randel
author_facet Lund, Andrea
Andersen, Kasper Jarlhelt
Meier, Michelle
Pedersen, Marie Ingemann
Knudsen, Anders Riegels
Kirkegård, Jakob
Mortensen, Frank Viborg
Nyengaard, Jens Randel
author_sort Lund, Andrea
collection PubMed
description The upper limit for partial hepatectomy (PH) in rats is 90%, which is associated with an increased risk of post-hepatectomy liver failure (PHLF), correlating with high mortality. Sixty-eight rats were randomized to 90% PH, sham operation, or no surgery. Further block randomization was performed to determine the time of euthanasia, whether 12, 24, or 48 h after surgery. A general distress score (GDS) was calculated to distinguish between rats with reversible (GDS < 10) and irreversible PHLF (GDS ≥ 10). At euthanasia, the liver remnant and blood were collected. Liver-specific biochemistry and regeneration ratio were measured. Hepatocyte proliferation and volume were estimated using stereological methods. All rats subjected to 90% experienced biochemical PHLF. The biochemical and morphological liver responses did not differ between the groups until 48 h after surgery. At 48 h, liver regeneration and function were significantly improved in survivors. The peak mean regeneration ratio was 15% for rats with irreversible PHLF compared to 26% for rats with reversible PHLF. The 90% PH rat model was associated with PHLF and high mortality. Irreversible PHLF was characterized by impaired liver regeneration capacity and an insufficient ability to metabolize ammonia.
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spelling pubmed-104399102023-08-21 Biochemical and morphological responses to post-hepatectomy liver failure in rats Lund, Andrea Andersen, Kasper Jarlhelt Meier, Michelle Pedersen, Marie Ingemann Knudsen, Anders Riegels Kirkegård, Jakob Mortensen, Frank Viborg Nyengaard, Jens Randel Sci Rep Article The upper limit for partial hepatectomy (PH) in rats is 90%, which is associated with an increased risk of post-hepatectomy liver failure (PHLF), correlating with high mortality. Sixty-eight rats were randomized to 90% PH, sham operation, or no surgery. Further block randomization was performed to determine the time of euthanasia, whether 12, 24, or 48 h after surgery. A general distress score (GDS) was calculated to distinguish between rats with reversible (GDS < 10) and irreversible PHLF (GDS ≥ 10). At euthanasia, the liver remnant and blood were collected. Liver-specific biochemistry and regeneration ratio were measured. Hepatocyte proliferation and volume were estimated using stereological methods. All rats subjected to 90% experienced biochemical PHLF. The biochemical and morphological liver responses did not differ between the groups until 48 h after surgery. At 48 h, liver regeneration and function were significantly improved in survivors. The peak mean regeneration ratio was 15% for rats with irreversible PHLF compared to 26% for rats with reversible PHLF. The 90% PH rat model was associated with PHLF and high mortality. Irreversible PHLF was characterized by impaired liver regeneration capacity and an insufficient ability to metabolize ammonia. Nature Publishing Group UK 2023-08-19 /pmc/articles/PMC10439910/ /pubmed/37598250 http://dx.doi.org/10.1038/s41598-023-40736-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lund, Andrea
Andersen, Kasper Jarlhelt
Meier, Michelle
Pedersen, Marie Ingemann
Knudsen, Anders Riegels
Kirkegård, Jakob
Mortensen, Frank Viborg
Nyengaard, Jens Randel
Biochemical and morphological responses to post-hepatectomy liver failure in rats
title Biochemical and morphological responses to post-hepatectomy liver failure in rats
title_full Biochemical and morphological responses to post-hepatectomy liver failure in rats
title_fullStr Biochemical and morphological responses to post-hepatectomy liver failure in rats
title_full_unstemmed Biochemical and morphological responses to post-hepatectomy liver failure in rats
title_short Biochemical and morphological responses to post-hepatectomy liver failure in rats
title_sort biochemical and morphological responses to post-hepatectomy liver failure in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439910/
https://www.ncbi.nlm.nih.gov/pubmed/37598250
http://dx.doi.org/10.1038/s41598-023-40736-y
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