Avaliação da lesão isquêmica normotérmica do fígado: papel da oclusão do ducto biliar principal e da N-acetilcisteína
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , |
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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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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1814268405186822144 |