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Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model

BACKGROUND: The aim of this study was to evaluate the effects of the antioxidant allopurinol and ischemic post-conditioning on the deleterious effects of ischemia followed by reperfusion (I/R) in a standardized model of ischemia involving infra-renal aortic occlusion in rats. METHODS: The animals we...

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Autores principales: Brandão, Rafael Inácio, Gomes, Ricardo Zanetti, Lopes, Luana, Linhares, Filipe Silva, Vellosa, José Carlos Rebuglio, Paludo, Katia Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266249/
https://www.ncbi.nlm.nih.gov/pubmed/30295166
http://dx.doi.org/10.1177/1753944718803309
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author Brandão, Rafael Inácio
Gomes, Ricardo Zanetti
Lopes, Luana
Linhares, Filipe Silva
Vellosa, José Carlos Rebuglio
Paludo, Katia Sabrina
author_facet Brandão, Rafael Inácio
Gomes, Ricardo Zanetti
Lopes, Luana
Linhares, Filipe Silva
Vellosa, José Carlos Rebuglio
Paludo, Katia Sabrina
author_sort Brandão, Rafael Inácio
collection PubMed
description BACKGROUND: The aim of this study was to evaluate the effects of the antioxidant allopurinol and ischemic post-conditioning on the deleterious effects of ischemia followed by reperfusion (I/R) in a standardized model of ischemia involving infra-renal aortic occlusion in rats. METHODS: The animals were randomly divided into five groups: (A) animals not subjected to ischemia; (B) animals subjected to 2 h of ischemia and reperfusion only once; (C) animals given an allopurinol dose by gavage, then subjected to 2 h of ischemia and reperfusion only once; (D) animals subjected to 2 h of ischemia and post-conditioning and (E) animals that received allopurinol, then subjected to 2 h of ischemia and post-conditioning. The blood samples and small intestine segments were harvested for analysis after 3 days. RESULTS: The protective effects of the use of allopurinol and ischemic post-conditioning were observed by measuring aspartate aminotransferase, alanine aminotransferase and lactate levels. The benefits of post-conditioning were evident from the total antioxidant capacity and creatinine levels, but these could not ascertain any positive effects of allopurinol. The histological analysis of mesentery revealed that both methods were effective in minimizing the harmful effects of the ischemia and reperfusion process. CONCLUSION: Individual protocols significantly reduced I/R systemic injuries, but no additional protection was observed when the two strategies were combined.
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spelling pubmed-62662492018-12-04 Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model Brandão, Rafael Inácio Gomes, Ricardo Zanetti Lopes, Luana Linhares, Filipe Silva Vellosa, José Carlos Rebuglio Paludo, Katia Sabrina Ther Adv Cardiovasc Dis Original Research BACKGROUND: The aim of this study was to evaluate the effects of the antioxidant allopurinol and ischemic post-conditioning on the deleterious effects of ischemia followed by reperfusion (I/R) in a standardized model of ischemia involving infra-renal aortic occlusion in rats. METHODS: The animals were randomly divided into five groups: (A) animals not subjected to ischemia; (B) animals subjected to 2 h of ischemia and reperfusion only once; (C) animals given an allopurinol dose by gavage, then subjected to 2 h of ischemia and reperfusion only once; (D) animals subjected to 2 h of ischemia and post-conditioning and (E) animals that received allopurinol, then subjected to 2 h of ischemia and post-conditioning. The blood samples and small intestine segments were harvested for analysis after 3 days. RESULTS: The protective effects of the use of allopurinol and ischemic post-conditioning were observed by measuring aspartate aminotransferase, alanine aminotransferase and lactate levels. The benefits of post-conditioning were evident from the total antioxidant capacity and creatinine levels, but these could not ascertain any positive effects of allopurinol. The histological analysis of mesentery revealed that both methods were effective in minimizing the harmful effects of the ischemia and reperfusion process. CONCLUSION: Individual protocols significantly reduced I/R systemic injuries, but no additional protection was observed when the two strategies were combined. SAGE Publications 2018-10-08 /pmc/articles/PMC6266249/ /pubmed/30295166 http://dx.doi.org/10.1177/1753944718803309 Text en © The Author(s), 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Brandão, Rafael Inácio
Gomes, Ricardo Zanetti
Lopes, Luana
Linhares, Filipe Silva
Vellosa, José Carlos Rebuglio
Paludo, Katia Sabrina
Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title_full Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title_fullStr Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title_full_unstemmed Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title_short Remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
title_sort remote post-conditioning and allopurinol reduce ischemia-reperfusion injury in an infra-renal ischemia model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266249/
https://www.ncbi.nlm.nih.gov/pubmed/30295166
http://dx.doi.org/10.1177/1753944718803309
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