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

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...

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Autores principales: la Garza, Francisco Javier Guzmán-de, Ibarra-Hernández, Juan Manuel, Cordero-Pérez, Paula, Villegas-Quintero, Pablo, Villarreal-Ovalle, Claudia Ivette, Torres-González, Liliana, Oliva-Sosa, Norma Edith, Alarcón-Galván, Gabriela, Fernández-Garza, Nancy Esthela, Muñoz-Espinosa, Linda Elsa, Cámara-Lemarroy, Carlos Rodrigo, Carrillo-Arriaga, José Gerardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715035/
https://www.ncbi.nlm.nih.gov/pubmed/23917671
http://dx.doi.org/10.6061/clinics/2013(07)23
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author la Garza, Francisco Javier Guzmán-de
Ibarra-Hernández, Juan Manuel
Cordero-Pérez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-González, Liliana
Oliva-Sosa, Norma Edith
Alarcón-Galván, Gabriela
Fernández-Garza, Nancy Esthela
Muñoz-Espinosa, Linda Elsa
Cámara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, José Gerardo
author_facet la Garza, Francisco Javier Guzmán-de
Ibarra-Hernández, Juan Manuel
Cordero-Pérez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-González, Liliana
Oliva-Sosa, Norma Edith
Alarcón-Galván, Gabriela
Fernández-Garza, Nancy Esthela
Muñoz-Espinosa, Linda Elsa
Cámara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, José Gerardo
author_sort la Garza, Francisco Javier Guzmán-de
collection PubMed
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.
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spelling pubmed-37150352013-07-22 Temporal relationship of serum markers and tissue damage during acute intestinal ischemia/reperfusion la Garza, Francisco Javier Guzmán-de Ibarra-Hernández, Juan Manuel Cordero-Pérez, Paula Villegas-Quintero, Pablo Villarreal-Ovalle, Claudia Ivette Torres-González, Liliana Oliva-Sosa, Norma Edith Alarcón-Galván, Gabriela Fernández-Garza, Nancy Esthela Muñoz-Espinosa, Linda Elsa Cámara-Lemarroy, Carlos Rodrigo Carrillo-Arriaga, José Gerardo Clinics (Sao Paulo) Basic Research 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. Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2013-07 /pmc/articles/PMC3715035/ /pubmed/23917671 http://dx.doi.org/10.6061/clinics/2013(07)23 Text en Copyright © 2013 Hospital das Clínicas da FMUSP http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
la Garza, Francisco Javier Guzmán-de
Ibarra-Hernández, Juan Manuel
Cordero-Pérez, Paula
Villegas-Quintero, Pablo
Villarreal-Ovalle, Claudia Ivette
Torres-González, Liliana
Oliva-Sosa, Norma Edith
Alarcón-Galván, Gabriela
Fernández-Garza, Nancy Esthela
Muñoz-Espinosa, Linda Elsa
Cámara-Lemarroy, Carlos Rodrigo
Carrillo-Arriaga, José Gerardo
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
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_short 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
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715035/
https://www.ncbi.nlm.nih.gov/pubmed/23917671
http://dx.doi.org/10.6061/clinics/2013(07)23
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