Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína

Detalhes bibliográficos
Autor(a) principal: Medeiros, Susi Heliene Lauz
Data de Publicação: 2005
Outros Autores: Montero, Edna Frasson de Souza [UNIFESP], Gomes, Lígia Ferreira, Taha, Murched Omar [UNIFESP], Junqueira, Virginia Berlanga Campos [UNIFESP], Simões, Manuel de Jesus [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0100-69912005000400002
http://repositorio.unifesp.br/handle/11600/2628
Resumo: BACKGROUND: The aim of this study was to investigate the effect of N-Acetylcysteine (NAC) on the hepatic ischemia injury. METHODS: Thirty eight male EPM-1 Wistar rats were divided in four groups: G1 and G2 with ischemia time of 30 min.; groups 3 and 4 were submitted to 30 min of ischemia and bile duct was not clamped. Animals from groups 2 and 4 received NAC, 150mg.Kg-1 bw, by IV injection, 15 min. before procedure. Blood samples were collected before and after ischemia and liver function was evaluated by enzymatic measurement. Hepatic samples were processed to GSH/GSSG, light and electronic microscopy evaluation. Non-parametric tests were applied to the statistical analysis (p < 0.05). RESULTS: Enzymatic increase were higher when NAC was absent. There was no protection by NAC when bile duct was absent nor when bile duct was not clamped. Under light microscopy there was significant difference in the groups S/NAC X C/NAC, showing that group C/NAC maintained better parenchyma architecture during ischemia time, independent on bile duct clamp. Under electronic microscopy, the groups C/NAC and those without bile duct clamping showed preserved cellular arquitecture. NAC did not alter the relationship between reduced glutathione / oxidated gluthatione (GSH/GSSG). CONCLUSION: NAC is able to protect hepatic parenquime during normothermic ischemia and we purpose that such mechanism is related to a direct reaction of NAC with nitric oxide (NO).
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spelling Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteínaEvaluation of the normothermic ischemic liver injury: the role of main biliary duct occlusion and N-acetylcysteineAcetylcysteineIschemiaLiverRats, WistarAcetilcisteínaIsquemiaFígadoRatos WistarBACKGROUND: The aim of this study was to investigate the effect of N-Acetylcysteine (NAC) on the hepatic ischemia injury. METHODS: Thirty eight male EPM-1 Wistar rats were divided in four groups: G1 and G2 with ischemia time of 30 min.; groups 3 and 4 were submitted to 30 min of ischemia and bile duct was not clamped. Animals from groups 2 and 4 received NAC, 150mg.Kg-1 bw, by IV injection, 15 min. before procedure. Blood samples were collected before and after ischemia and liver function was evaluated by enzymatic measurement. Hepatic samples were processed to GSH/GSSG, light and electronic microscopy evaluation. Non-parametric tests were applied to the statistical analysis (p < 0.05). RESULTS: Enzymatic increase were higher when NAC was absent. There was no protection by NAC when bile duct was absent nor when bile duct was not clamped. Under light microscopy there was significant difference in the groups S/NAC X C/NAC, showing that group C/NAC maintained better parenchyma architecture during ischemia time, independent on bile duct clamp. Under electronic microscopy, the groups C/NAC and those without bile duct clamping showed preserved cellular arquitecture. NAC did not alter the relationship between reduced glutathione / oxidated gluthatione (GSH/GSSG). CONCLUSION: NAC is able to protect hepatic parenquime during normothermic ischemia and we purpose that such mechanism is related to a direct reaction of NAC with nitric oxide (NO).OBJETIVO: Estudar o efeito da N-acetilcisteína (NAC) na isquemia hepática. MÉTODO: Trinta e oito ratos machos EPM-1 Wistar foram distribuídos em quatro grupos. Nos Grupos 1 e 2 foi realizado 30 min de clampeamento do hilo hepático, e nos Grupos 3 e 4 os animais foram submetidos a 30 minutos de isquemia sem clampleamento do ducto biliar. Os animais dos Grupos 2 e 4 receberam 150mg.Kg-1 de NAC, endovenoso, 15 minutos antes do procedimento. Colheu-se sangue antes do procedimento e após o clampeamento do pedículo para a dosagem enzimática. Amostras de fígado foram coletadas para dosagem de glutationa, microscopia óptica e eletrônica. No estudo estatístico aplicaram-se testes não paramétricos, p < 0,05. RESULTADOS: O aumento das enzimas foi menor quando se administrou NAC, sendo semelhante na ausência do clampeamento da via biliar. À microscopia óptica houve diferença significante dos grupos S/NAC X C/NAC, mostrando que o grupo C/NAC manteve a arquitetura do parênquima durante a isquemia, independente do clampeamento do ducto biliar. Na microscopia eletrônica os grupos C/NAC e os sem clampeamento do ducto biliar apresentaram arquitetura celular preservada. A NAC não alterou a relação de glutationa reduzida/ glutationa oxidada (GSH/GSSG). CONCLUSÕES: A NAC é capaz de proteger o parênquima hepático durante a isquemia normotérmica e propõe-se que o mecanismo seja por reação direta da NAC com o óxido nítrico (NO).FURG Departamento de CirurgiaUNIFESP-EPM Departamento de CirurgiaUSP Departamento de Análises Clínicas e ToxicológicasUNIFESP-EPM Departamento de Medicina InternaUNIFESP-EPM Departamento de MorfologiaUNIFESP, EPM, Depto. de CirurgiaUNIFESP, EPM Depto. de Medicina InternaUNIFESP, EPM Depto. de MorfologiaSciELOColégio Brasileiro de CirurgiõesFURG Departamento de CirurgiaUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Medeiros, Susi Heliene LauzMontero, Edna Frasson de Souza [UNIFESP]Gomes, Lígia FerreiraTaha, Murched Omar [UNIFESP]Junqueira, Virginia Berlanga Campos [UNIFESP]Simões, Manuel de Jesus [UNIFESP]2015-06-14T13:31:41Z2015-06-14T13:31:41Z2005-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion168-172application/pdfhttp://dx.doi.org/10.1590/S0100-69912005000400002Revista do Colégio Brasileiro de Cirurgiões. Colégio Brasileiro de Cirurgiões, v. 32, n. 4, p. 168-172, 2005.10.1590/S0100-69912005000400002S0100-69912005000400002.pdf0100-6991S0100-69912005000400002http://repositorio.unifesp.br/handle/11600/2628porRevista do Colégio Brasileiro de Cirurgiõesinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T16:29:25Zoai:repositorio.unifesp.br/:11600/2628Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T16:29:25Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
Evaluation of the normothermic ischemic liver injury: the role of main biliary duct occlusion and N-acetylcysteine
title Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
spellingShingle Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
Medeiros, Susi Heliene Lauz
Acetylcysteine
Ischemia
Liver
Rats, Wistar
Acetilcisteína
Isquemia
Fígado
Ratos Wistar
title_short Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
title_full Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
title_fullStr Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
title_full_unstemmed Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
title_sort Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
author Medeiros, Susi Heliene Lauz
author_facet Medeiros, Susi Heliene Lauz
Montero, Edna Frasson de Souza [UNIFESP]
Gomes, Lígia Ferreira
Taha, Murched Omar [UNIFESP]
Junqueira, Virginia Berlanga Campos [UNIFESP]
Simões, Manuel de Jesus [UNIFESP]
author_role author
author2 Montero, Edna Frasson de Souza [UNIFESP]
Gomes, Lígia Ferreira
Taha, Murched Omar [UNIFESP]
Junqueira, Virginia Berlanga Campos [UNIFESP]
Simões, Manuel de Jesus [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv FURG Departamento de Cirurgia
Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Medeiros, Susi Heliene Lauz
Montero, Edna Frasson de Souza [UNIFESP]
Gomes, Lígia Ferreira
Taha, Murched Omar [UNIFESP]
Junqueira, Virginia Berlanga Campos [UNIFESP]
Simões, Manuel de Jesus [UNIFESP]
dc.subject.por.fl_str_mv Acetylcysteine
Ischemia
Liver
Rats, Wistar
Acetilcisteína
Isquemia
Fígado
Ratos Wistar
topic Acetylcysteine
Ischemia
Liver
Rats, Wistar
Acetilcisteína
Isquemia
Fígado
Ratos Wistar
description BACKGROUND: The aim of this study was to investigate the effect of N-Acetylcysteine (NAC) on the hepatic ischemia injury. METHODS: Thirty eight male EPM-1 Wistar rats were divided in four groups: G1 and G2 with ischemia time of 30 min.; groups 3 and 4 were submitted to 30 min of ischemia and bile duct was not clamped. Animals from groups 2 and 4 received NAC, 150mg.Kg-1 bw, by IV injection, 15 min. before procedure. Blood samples were collected before and after ischemia and liver function was evaluated by enzymatic measurement. Hepatic samples were processed to GSH/GSSG, light and electronic microscopy evaluation. Non-parametric tests were applied to the statistical analysis (p < 0.05). RESULTS: Enzymatic increase were higher when NAC was absent. There was no protection by NAC when bile duct was absent nor when bile duct was not clamped. Under light microscopy there was significant difference in the groups S/NAC X C/NAC, showing that group C/NAC maintained better parenchyma architecture during ischemia time, independent on bile duct clamp. Under electronic microscopy, the groups C/NAC and those without bile duct clamping showed preserved cellular arquitecture. NAC did not alter the relationship between reduced glutathione / oxidated gluthatione (GSH/GSSG). CONCLUSION: NAC is able to protect hepatic parenquime during normothermic ischemia and we purpose that such mechanism is related to a direct reaction of NAC with nitric oxide (NO).
publishDate 2005
dc.date.none.fl_str_mv 2005-08-01
2015-06-14T13:31:41Z
2015-06-14T13:31:41Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0100-69912005000400002
Revista do Colégio Brasileiro de Cirurgiões. Colégio Brasileiro de Cirurgiões, v. 32, n. 4, p. 168-172, 2005.
10.1590/S0100-69912005000400002
S0100-69912005000400002.pdf
0100-6991
S0100-69912005000400002
http://repositorio.unifesp.br/handle/11600/2628
url http://dx.doi.org/10.1590/S0100-69912005000400002
http://repositorio.unifesp.br/handle/11600/2628
identifier_str_mv Revista do Colégio Brasileiro de Cirurgiões. Colégio Brasileiro de Cirurgiões, v. 32, n. 4, p. 168-172, 2005.
10.1590/S0100-69912005000400002
S0100-69912005000400002.pdf
0100-6991
S0100-69912005000400002
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista do Colégio Brasileiro de Cirurgiões
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 168-172
application/pdf
dc.publisher.none.fl_str_mv Colégio Brasileiro de Cirurgiões
publisher.none.fl_str_mv Colégio Brasileiro de Cirurgiões
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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