Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode

Detalhes bibliográficos
Autor(a) principal: Gabiatti, Gémerson
Data de Publicação: 2018
Outros Autores: Grezzana Filho, Tomáz de Jesus Maria, Cerski, Carlos Thadeu Schmidt, Bofill, Carlos Medeiros, Valle, Stella de Faria, Corso, Carlos Otavio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/200777
Resumo: Purpose: To develop a new 24 hour extended liver ischemia and reperfusion (LIR) model analyzing the late biochemical and histopathological results of the isolated and combined application of recognized hepatoprotective mechanisms. In addition, we used a new stratification with zoning to classify the histological lesion. Methods: A modified animal model of severe hepatic damage produced through 90 minutes of segmental ischemia (70% of the organ) and posterior observation for 24 hours of reperfusion, submitted to ischemic preconditioning (IPC) and topical hypothermia (TH) at 26ºC, in isolation or in combination, during the procedure. Data from intraoperative biometric parameters, besides of late biochemical markers and histopathological findings, both at 24 hours evolution time, were compared with control (C) and normothermic ischemia (NI) groups. Results: All groups were homogeneous with respect to intraoperative physiological parameters. There were no losses once the model was stablished. Animals subjected to NI and IPC had worse biochemical (gamma-glutamyl transpeptidase, alkaline phosphatase, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, direct bilirubin, and total bilirubin) and histopathological scores (modified Suzuki score) compared to those of control groups and groups with isolated or associated TH (p < 0.05). Conclusion: The new extended model demonstrates liver ischemia and reperfusion at 24 hour of evolution and, in this extreme scenario, only the groups subjected to topical hypothermia, combined with ischemic preconditioning or alone, had better outcomes than those subjected to only ischemic preconditioning and normothermic ischemia, reaching similar biochemical and histopathological scores to those of the control group.
id UFRGS-2_5c632be5883b9b5dbe63b0e01fad96ab
oai_identifier_str oai:www.lume.ufrgs.br:10183/200777
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Gabiatti, GémersonGrezzana Filho, Tomáz de Jesus MariaCerski, Carlos Thadeu SchmidtBofill, Carlos MedeirosValle, Stella de FariaCorso, Carlos Otavio2019-10-17T03:52:03Z20180102-8650http://hdl.handle.net/10183/200777001104484Purpose: To develop a new 24 hour extended liver ischemia and reperfusion (LIR) model analyzing the late biochemical and histopathological results of the isolated and combined application of recognized hepatoprotective mechanisms. In addition, we used a new stratification with zoning to classify the histological lesion. Methods: A modified animal model of severe hepatic damage produced through 90 minutes of segmental ischemia (70% of the organ) and posterior observation for 24 hours of reperfusion, submitted to ischemic preconditioning (IPC) and topical hypothermia (TH) at 26ºC, in isolation or in combination, during the procedure. Data from intraoperative biometric parameters, besides of late biochemical markers and histopathological findings, both at 24 hours evolution time, were compared with control (C) and normothermic ischemia (NI) groups. Results: All groups were homogeneous with respect to intraoperative physiological parameters. There were no losses once the model was stablished. Animals subjected to NI and IPC had worse biochemical (gamma-glutamyl transpeptidase, alkaline phosphatase, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, direct bilirubin, and total bilirubin) and histopathological scores (modified Suzuki score) compared to those of control groups and groups with isolated or associated TH (p < 0.05). Conclusion: The new extended model demonstrates liver ischemia and reperfusion at 24 hour of evolution and, in this extreme scenario, only the groups subjected to topical hypothermia, combined with ischemic preconditioning or alone, had better outcomes than those subjected to only ischemic preconditioning and normothermic ischemia, reaching similar biochemical and histopathological scores to those of the control group.application/pdfengActa cirúrgica brasileira. Vol. 33, no. 10 (2018), p. 924-934IsquemiaHipotermiaRatosModelos animaisReperfusãoFígadoPrecondicionamento isquêmicoIschemic preconditioningIschemiaReperfusionLiverHypothermiaRatsTopical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour modeinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001104484.pdf.txt001104484.pdf.txtExtracted Texttext/plain37834http://www.lume.ufrgs.br/bitstream/10183/200777/2/001104484.pdf.txt5a260b72fdacb599fc7c3c9462063532MD52ORIGINAL001104484.pdfTexto completo (inglês)application/pdf591447http://www.lume.ufrgs.br/bitstream/10183/200777/1/001104484.pdfa1c6848a83acaf81ae8b86d9bedc2b6aMD5110183/2007772019-10-18 03:54:25.015769oai:www.lume.ufrgs.br:10183/200777Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2019-10-18T06:54:25Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
title Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
spellingShingle Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
Gabiatti, Gémerson
Isquemia
Hipotermia
Ratos
Modelos animais
Reperfusão
Fígado
Precondicionamento isquêmico
Ischemic preconditioning
Ischemia
Reperfusion
Liver
Hypothermia
Rats
title_short Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
title_full Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
title_fullStr Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
title_full_unstemmed Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
title_sort Topical hepatic hypothermia associated with ischemic preconditioning : histopathological and biochemical analysis of ischemia reperfusion damage in a 24 hour mode
author Gabiatti, Gémerson
author_facet Gabiatti, Gémerson
Grezzana Filho, Tomáz de Jesus Maria
Cerski, Carlos Thadeu Schmidt
Bofill, Carlos Medeiros
Valle, Stella de Faria
Corso, Carlos Otavio
author_role author
author2 Grezzana Filho, Tomáz de Jesus Maria
Cerski, Carlos Thadeu Schmidt
Bofill, Carlos Medeiros
Valle, Stella de Faria
Corso, Carlos Otavio
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Gabiatti, Gémerson
Grezzana Filho, Tomáz de Jesus Maria
Cerski, Carlos Thadeu Schmidt
Bofill, Carlos Medeiros
Valle, Stella de Faria
Corso, Carlos Otavio
dc.subject.por.fl_str_mv Isquemia
Hipotermia
Ratos
Modelos animais
Reperfusão
Fígado
Precondicionamento isquêmico
topic Isquemia
Hipotermia
Ratos
Modelos animais
Reperfusão
Fígado
Precondicionamento isquêmico
Ischemic preconditioning
Ischemia
Reperfusion
Liver
Hypothermia
Rats
dc.subject.eng.fl_str_mv Ischemic preconditioning
Ischemia
Reperfusion
Liver
Hypothermia
Rats
description Purpose: To develop a new 24 hour extended liver ischemia and reperfusion (LIR) model analyzing the late biochemical and histopathological results of the isolated and combined application of recognized hepatoprotective mechanisms. In addition, we used a new stratification with zoning to classify the histological lesion. Methods: A modified animal model of severe hepatic damage produced through 90 minutes of segmental ischemia (70% of the organ) and posterior observation for 24 hours of reperfusion, submitted to ischemic preconditioning (IPC) and topical hypothermia (TH) at 26ºC, in isolation or in combination, during the procedure. Data from intraoperative biometric parameters, besides of late biochemical markers and histopathological findings, both at 24 hours evolution time, were compared with control (C) and normothermic ischemia (NI) groups. Results: All groups were homogeneous with respect to intraoperative physiological parameters. There were no losses once the model was stablished. Animals subjected to NI and IPC had worse biochemical (gamma-glutamyl transpeptidase, alkaline phosphatase, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, direct bilirubin, and total bilirubin) and histopathological scores (modified Suzuki score) compared to those of control groups and groups with isolated or associated TH (p < 0.05). Conclusion: The new extended model demonstrates liver ischemia and reperfusion at 24 hour of evolution and, in this extreme scenario, only the groups subjected to topical hypothermia, combined with ischemic preconditioning or alone, had better outcomes than those subjected to only ischemic preconditioning and normothermic ischemia, reaching similar biochemical and histopathological scores to those of the control group.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2019-10-17T03:52:03Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/other
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/200777
dc.identifier.issn.pt_BR.fl_str_mv 0102-8650
dc.identifier.nrb.pt_BR.fl_str_mv 001104484
identifier_str_mv 0102-8650
001104484
url http://hdl.handle.net/10183/200777
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Acta cirúrgica brasileira. Vol. 33, no. 10 (2018), p. 924-934
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/200777/2/001104484.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/200777/1/001104484.pdf
bitstream.checksum.fl_str_mv 5a260b72fdacb599fc7c3c9462063532
a1c6848a83acaf81ae8b86d9bedc2b6a
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1801224976951410688