Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion

Detalhes bibliográficos
Autor(a) principal: la Garza, Francisco Javier Guzman-de
Data de Publicação: 2013
Outros Autores: Ibarra-Hernandez, Juan Manuel, Cordero-Perez, Paula, Villegas-Quintero, Pablo, Villarreal-Ovalle, Claudia Ivette, Torres-Gonzalez, Liliana, Oliva-Sosa, Norma Edith, Alarcon-Galvan, Gabriela, Fernandez-Garza, Nancy Esthela, Munoz-Espinosa, Linda Elsa, Camara-Lemarroy, Carlos Rodrigo, Carrillo-Arriaga, Jose Gerardo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/76936
Resumo: OBJECTIVE: It is essential to identify a serological marker of injury in order to study the pathophysiology of intestinal ischemia reperfusion. In this work, we studied the evolution of several serological markers after intestinal ischemia reperfusion injury in rats. The markers of non-specific cell damage were aspartate aminotransferase, alanine aminotransaminase, and lactic dehydrogenase, the markers of inflammation were tumor necrosis factor alpha, interleukin-6, and interleukin-1 beta, and the markers of intestinal mucosal damage were intestinal fatty acid binding protein and D-lactate. We used Chiús classification to grade the histopathological damage. METHODS: We studied 35 Wistar rats divided into groups according to reperfusion time. The superior mesenteric artery was clamped for 30 minutes, and blood and biopsies were collected at 1, 3, 6, 12, 24, and 48 hours after reperfusion. We plotted the mean ± standard deviation and compared the baseline and maximum values for each marker using Student's t-test. RESULTS: The maximum values of interleukin-1 beta and lactic dehydrogenase were present before the maximal histopathological damage. The maximum tumor necrosis factor alpha and D-lactate expressions coincided with histopathological damage. Alanine aminotransaminase and aspartate aminotransferase had a maximum expression level that increased following the histopathological damage. The maximum expressions of interluken-6 and intestinal fatty acid binding protein were not significantly different from the Sham treated group. CONCLUSION: For the evaluation of injury secondary to acute intestinal ischemia reperfusion with a 30 minute ischemia period, we recommend performing histopathological grading, quantification of D-lactate, which is synthesized by intestinal bacteria and is considered an indicator of mucosal injury, and quantification of tumor necrosis factor alpha as indicators of acute inflammation three hours after reperfusion.
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spelling Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusionOBJECTIVE: It is essential to identify a serological marker of injury in order to study the pathophysiology of intestinal ischemia reperfusion. In this work, we studied the evolution of several serological markers after intestinal ischemia reperfusion injury in rats. The markers of non-specific cell damage were aspartate aminotransferase, alanine aminotransaminase, and lactic dehydrogenase, the markers of inflammation were tumor necrosis factor alpha, interleukin-6, and interleukin-1 beta, and the markers of intestinal mucosal damage were intestinal fatty acid binding protein and D-lactate. We used Chiús classification to grade the histopathological damage. METHODS: We studied 35 Wistar rats divided into groups according to reperfusion time. The superior mesenteric artery was clamped for 30 minutes, and blood and biopsies were collected at 1, 3, 6, 12, 24, and 48 hours after reperfusion. We plotted the mean ± standard deviation and compared the baseline and maximum values for each marker using Student's t-test. RESULTS: The maximum values of interleukin-1 beta and lactic dehydrogenase were present before the maximal histopathological damage. The maximum tumor necrosis factor alpha and D-lactate expressions coincided with histopathological damage. Alanine aminotransaminase and aspartate aminotransferase had a maximum expression level that increased following the histopathological damage. The maximum expressions of interluken-6 and intestinal fatty acid binding protein were not significantly different from the Sham treated group. CONCLUSION: For the evaluation of injury secondary to acute intestinal ischemia reperfusion with a 30 minute ischemia period, we recommend performing histopathological grading, quantification of D-lactate, which is synthesized by intestinal bacteria and is considered an indicator of mucosal injury, and quantification of tumor necrosis factor alpha as indicators of acute inflammation three hours after reperfusion.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2013-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/7693610.1590/clin.v68i7.76936Clinics; Vol. 68 No. 7 (2013); 1034-1038Clinics; v. 68 n. 7 (2013); 1034-1038Clinics; Vol. 68 Núm. 7 (2013); 1034-10381980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/76936/80797la Garza, Francisco Javier Guzman-deIbarra-Hernandez, Juan ManuelCordero-Perez, PaulaVillegas-Quintero, PabloVillarreal-Ovalle, Claudia IvetteTorres-Gonzalez, LilianaOliva-Sosa, Norma EdithAlarcon-Galvan, GabrielaFernandez-Garza, Nancy EsthelaMunoz-Espinosa, Linda ElsaCamara-Lemarroy, Carlos RodrigoCarrillo-Arriaga, Jose Gerardoinfo:eu-repo/semantics/openAccess2014-03-24T11:50:37Zoai:revistas.usp.br:article/76936Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2014-03-24T11:50:37Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
title Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
spellingShingle Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
la Garza, Francisco Javier Guzman-de
title_short Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
title_full Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
title_fullStr Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
title_full_unstemmed Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
title_sort Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion
author la Garza, Francisco Javier Guzman-de
author_facet la Garza, Francisco Javier Guzman-de
Ibarra-Hernandez, Juan Manuel
Cordero-Perez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-Gonzalez, Liliana
Oliva-Sosa, Norma Edith
Alarcon-Galvan, Gabriela
Fernandez-Garza, Nancy Esthela
Munoz-Espinosa, Linda Elsa
Camara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, Jose Gerardo
author_role author
author2 Ibarra-Hernandez, Juan Manuel
Cordero-Perez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-Gonzalez, Liliana
Oliva-Sosa, Norma Edith
Alarcon-Galvan, Gabriela
Fernandez-Garza, Nancy Esthela
Munoz-Espinosa, Linda Elsa
Camara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, Jose Gerardo
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv la Garza, Francisco Javier Guzman-de
Ibarra-Hernandez, Juan Manuel
Cordero-Perez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-Gonzalez, Liliana
Oliva-Sosa, Norma Edith
Alarcon-Galvan, Gabriela
Fernandez-Garza, Nancy Esthela
Munoz-Espinosa, Linda Elsa
Camara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, Jose Gerardo
description OBJECTIVE: It is essential to identify a serological marker of injury in order to study the pathophysiology of intestinal ischemia reperfusion. In this work, we studied the evolution of several serological markers after intestinal ischemia reperfusion injury in rats. The markers of non-specific cell damage were aspartate aminotransferase, alanine aminotransaminase, and lactic dehydrogenase, the markers of inflammation were tumor necrosis factor alpha, interleukin-6, and interleukin-1 beta, and the markers of intestinal mucosal damage were intestinal fatty acid binding protein and D-lactate. We used Chiús classification to grade the histopathological damage. METHODS: We studied 35 Wistar rats divided into groups according to reperfusion time. The superior mesenteric artery was clamped for 30 minutes, and blood and biopsies were collected at 1, 3, 6, 12, 24, and 48 hours after reperfusion. We plotted the mean ± standard deviation and compared the baseline and maximum values for each marker using Student's t-test. RESULTS: The maximum values of interleukin-1 beta and lactic dehydrogenase were present before the maximal histopathological damage. The maximum tumor necrosis factor alpha and D-lactate expressions coincided with histopathological damage. Alanine aminotransaminase and aspartate aminotransferase had a maximum expression level that increased following the histopathological damage. The maximum expressions of interluken-6 and intestinal fatty acid binding protein were not significantly different from the Sham treated group. CONCLUSION: For the evaluation of injury secondary to acute intestinal ischemia reperfusion with a 30 minute ischemia period, we recommend performing histopathological grading, quantification of D-lactate, which is synthesized by intestinal bacteria and is considered an indicator of mucosal injury, and quantification of tumor necrosis factor alpha as indicators of acute inflammation three hours after reperfusion.
publishDate 2013
dc.date.none.fl_str_mv 2013-07-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/76936
10.1590/clin.v68i7.76936
url https://www.revistas.usp.br/clinics/article/view/76936
identifier_str_mv 10.1590/clin.v68i7.76936
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/76936/80797
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.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 68 No. 7 (2013); 1034-1038
Clinics; v. 68 n. 7 (2013); 1034-1038
Clinics; Vol. 68 Núm. 7 (2013); 1034-1038
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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