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Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability

It was reported that prevention of acute portal overpressure in small-for-size livers by inflow modulation results in a better postoperative outcome. The aim is to investigate the impact of portal blood flow reduction by splenic artery ligation after major hepatectomy in a murine model. Forty-eight...

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Autores principales: Carrapita, Jorge, Abrantes, Ana Margarida, Campelos, Sofia, Gonçalves, Ana Cristina, Cardoso, Dulce, Sarmento-Ribeiro, Ana Bela, Rocha, Clara, Santos, Jorge Nunes, Botelho, Maria Filomena, Tralhão, José Guilherme, Farges, Olivier, Barbosa, Jorge Maciel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057079/
https://www.ncbi.nlm.nih.gov/pubmed/27725728
http://dx.doi.org/10.1038/srep34731
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author Carrapita, Jorge
Abrantes, Ana Margarida
Campelos, Sofia
Gonçalves, Ana Cristina
Cardoso, Dulce
Sarmento-Ribeiro, Ana Bela
Rocha, Clara
Santos, Jorge Nunes
Botelho, Maria Filomena
Tralhão, José Guilherme
Farges, Olivier
Barbosa, Jorge Maciel
author_facet Carrapita, Jorge
Abrantes, Ana Margarida
Campelos, Sofia
Gonçalves, Ana Cristina
Cardoso, Dulce
Sarmento-Ribeiro, Ana Bela
Rocha, Clara
Santos, Jorge Nunes
Botelho, Maria Filomena
Tralhão, José Guilherme
Farges, Olivier
Barbosa, Jorge Maciel
author_sort Carrapita, Jorge
collection PubMed
description It was reported that prevention of acute portal overpressure in small-for-size livers by inflow modulation results in a better postoperative outcome. The aim is to investigate the impact of portal blood flow reduction by splenic artery ligation after major hepatectomy in a murine model. Forty-eight rats were subjected to an 85% hepatectomy or 85% hepatectomy and splenic artery ligation. Both groups were evaluated at 24, 48, 72 and 120 post-operative hours: liver function, regeneration and viability. All methods and experiments were carried out in accordance with Coimbra University guidelines. Splenic artery ligation produces viability increase after 24 h, induces a relative decrease in oxidative stress during the first 48 hours, allows antioxidant capacity increment after 24 h, which is reflected in a decrease of half-time normalized liver curve at 48 h and at 72 h and in an increase of mitotic index between 48 h and 72 h. Splenic artery ligation combined with 85% hepatectomy in a murine model, allows portal inflow modulation, promoting an increase in hepatocellular viability and regeneration, without impairing the function, probably by inducing a less marked elevation of oxidative stress at first 48 hours.
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spelling pubmed-50570792016-10-24 Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability Carrapita, Jorge Abrantes, Ana Margarida Campelos, Sofia Gonçalves, Ana Cristina Cardoso, Dulce Sarmento-Ribeiro, Ana Bela Rocha, Clara Santos, Jorge Nunes Botelho, Maria Filomena Tralhão, José Guilherme Farges, Olivier Barbosa, Jorge Maciel Sci Rep Article It was reported that prevention of acute portal overpressure in small-for-size livers by inflow modulation results in a better postoperative outcome. The aim is to investigate the impact of portal blood flow reduction by splenic artery ligation after major hepatectomy in a murine model. Forty-eight rats were subjected to an 85% hepatectomy or 85% hepatectomy and splenic artery ligation. Both groups were evaluated at 24, 48, 72 and 120 post-operative hours: liver function, regeneration and viability. All methods and experiments were carried out in accordance with Coimbra University guidelines. Splenic artery ligation produces viability increase after 24 h, induces a relative decrease in oxidative stress during the first 48 hours, allows antioxidant capacity increment after 24 h, which is reflected in a decrease of half-time normalized liver curve at 48 h and at 72 h and in an increase of mitotic index between 48 h and 72 h. Splenic artery ligation combined with 85% hepatectomy in a murine model, allows portal inflow modulation, promoting an increase in hepatocellular viability and regeneration, without impairing the function, probably by inducing a less marked elevation of oxidative stress at first 48 hours. Nature Publishing Group 2016-10-11 /pmc/articles/PMC5057079/ /pubmed/27725728 http://dx.doi.org/10.1038/srep34731 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
Carrapita, Jorge
Abrantes, Ana Margarida
Campelos, Sofia
Gonçalves, Ana Cristina
Cardoso, Dulce
Sarmento-Ribeiro, Ana Bela
Rocha, Clara
Santos, Jorge Nunes
Botelho, Maria Filomena
Tralhão, José Guilherme
Farges, Olivier
Barbosa, Jorge Maciel
Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title_full Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title_fullStr Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title_full_unstemmed Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title_short Impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
title_sort impact of splenic artery ligation after major hepatectomy on liver function, regeneration and viability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5057079/
https://www.ncbi.nlm.nih.gov/pubmed/27725728
http://dx.doi.org/10.1038/srep34731
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