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Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours

PURPOSE: To investigate the effects of induction of selective liver hypothermia in a rodent model. METHODS: Seven male Wistar rats were subjected to 90 minutes of partial 70% liver ischemia and topic liver 26°C hypothermia (H group). Other seven male Wistar rats were subjected to 90 minutes of parti...

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Autores principales: Grezzana, Tomaz de Jesus Maria, Longo, Larisse, dos Santos, Jorge Luiz, Gabiatti, Gemerson, Boffil, Carlos, dos Santos, Emanuel Bendo, Cerski, Carlos Thadeu Schmidt, Chedid, Marcio Fernandes, Corso, Carlos Otavio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217597/
https://www.ncbi.nlm.nih.gov/pubmed/32428061
http://dx.doi.org/10.1590/s0102-865020200020000005
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author Grezzana, Tomaz de Jesus Maria
Longo, Larisse
dos Santos, Jorge Luiz
Gabiatti, Gemerson
Boffil, Carlos
dos Santos, Emanuel Bendo
Cerski, Carlos Thadeu Schmidt
Chedid, Marcio Fernandes
Corso, Carlos Otavio
author_facet Grezzana, Tomaz de Jesus Maria
Longo, Larisse
dos Santos, Jorge Luiz
Gabiatti, Gemerson
Boffil, Carlos
dos Santos, Emanuel Bendo
Cerski, Carlos Thadeu Schmidt
Chedid, Marcio Fernandes
Corso, Carlos Otavio
author_sort Grezzana, Tomaz de Jesus Maria
collection PubMed
description PURPOSE: To investigate the effects of induction of selective liver hypothermia in a rodent model. METHODS: Seven male Wistar rats were subjected to 90 minutes of partial 70% liver ischemia and topic liver 26°C hypothermia (H group). Other seven male Wistar rats were subjected to 90 minutes of partial 70% normothermic liver ischemia (N group). Five additional rats underwent a midline incision and section of liver ligaments under normothermic conditions and without any liver ischemia (sham group). All animals were sacrificed 24-h after reperfusion, and livers were sampled for analyses. Pathology sections were scored for sinusoidal congestion, ballooning, hepatocelllular necrosis and the presence of neutrophilic infiltrates. RESULTS: At the end of the experiment, liver tissue expressions of TNF-ɑ, IL-1β, iNOS and TNF-ɑ/IL-10 ratio were significantly reduced in the H group compared to N group, whereas IL-10 and eNOS were significantly increased in H group. Histopathological injury scores revealed a significant decrease in ischemia/reperfusion (I/R) injuries in H group. CONCLUSION: Selective liver hypothermia prevented I/R injury by inhibiting the release of inflammatory cytokines, preserves microcirculation, prevents hepatocellular necrosis and leukocyte infiltration, allowing maintenance of the liver architecture.
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spelling pubmed-72175972020-05-18 Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours Grezzana, Tomaz de Jesus Maria Longo, Larisse dos Santos, Jorge Luiz Gabiatti, Gemerson Boffil, Carlos dos Santos, Emanuel Bendo Cerski, Carlos Thadeu Schmidt Chedid, Marcio Fernandes Corso, Carlos Otavio Acta Cir Bras Original Article PURPOSE: To investigate the effects of induction of selective liver hypothermia in a rodent model. METHODS: Seven male Wistar rats were subjected to 90 minutes of partial 70% liver ischemia and topic liver 26°C hypothermia (H group). Other seven male Wistar rats were subjected to 90 minutes of partial 70% normothermic liver ischemia (N group). Five additional rats underwent a midline incision and section of liver ligaments under normothermic conditions and without any liver ischemia (sham group). All animals were sacrificed 24-h after reperfusion, and livers were sampled for analyses. Pathology sections were scored for sinusoidal congestion, ballooning, hepatocelllular necrosis and the presence of neutrophilic infiltrates. RESULTS: At the end of the experiment, liver tissue expressions of TNF-ɑ, IL-1β, iNOS and TNF-ɑ/IL-10 ratio were significantly reduced in the H group compared to N group, whereas IL-10 and eNOS were significantly increased in H group. Histopathological injury scores revealed a significant decrease in ischemia/reperfusion (I/R) injuries in H group. CONCLUSION: Selective liver hypothermia prevented I/R injury by inhibiting the release of inflammatory cytokines, preserves microcirculation, prevents hepatocellular necrosis and leukocyte infiltration, allowing maintenance of the liver architecture. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020-05-08 /pmc/articles/PMC7217597/ /pubmed/32428061 http://dx.doi.org/10.1590/s0102-865020200020000005 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
Grezzana, Tomaz de Jesus Maria
Longo, Larisse
dos Santos, Jorge Luiz
Gabiatti, Gemerson
Boffil, Carlos
dos Santos, Emanuel Bendo
Cerski, Carlos Thadeu Schmidt
Chedid, Marcio Fernandes
Corso, Carlos Otavio
Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title_full Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title_fullStr Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title_full_unstemmed Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title_short Induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in Wistar rats after 24 hours
title_sort induction of selective liver hypothermia prevents significant ischemia/reperfusion injury in wistar rats after 24 hours
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217597/
https://www.ncbi.nlm.nih.gov/pubmed/32428061
http://dx.doi.org/10.1590/s0102-865020200020000005
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