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The role of allopurinol's timing in the ischemia reperfusion injury of small intestine

INTRODUCTION: Allopurinol acts protectively in the ischemia reperfusion injury of the small intestine. The aim of this experimental study is to define the ideal time of administration of allopurinol, in experimental models of ischemia/reperfusion. MATERIALS AND METHODS: We used 46 rabbits that were...

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Autores principales: Sapalidis, Konstantinos, Papavramidis, Theodossis S, Gialamas, Eleftherios, Deligiannidis, Nikolaos, Tzioufa, Valentini, Papavramidis, Spiros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746444/
https://www.ncbi.nlm.nih.gov/pubmed/23960379
http://dx.doi.org/10.4103/0974-2700.115346
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author Sapalidis, Konstantinos
Papavramidis, Theodossis S
Gialamas, Eleftherios
Deligiannidis, Nikolaos
Tzioufa, Valentini
Papavramidis, Spiros
author_facet Sapalidis, Konstantinos
Papavramidis, Theodossis S
Gialamas, Eleftherios
Deligiannidis, Nikolaos
Tzioufa, Valentini
Papavramidis, Spiros
author_sort Sapalidis, Konstantinos
collection PubMed
description INTRODUCTION: Allopurinol acts protectively in the ischemia reperfusion injury of the small intestine. The aim of this experimental study is to define the ideal time of administration of allopurinol, in experimental models of ischemia/reperfusion. MATERIALS AND METHODS: We used 46 rabbits that were divided into four groups. Group A was the control. In Group B allopurinol was administered 10 min before ischemia and in Group C 2 min before reperfusion. In Group D, allopurinol was administered before ischemia and before reperfusion in half doses. Blood samples were collected at three different moments: (t(1)) prior to ischemia, (t(2)) prior to reperfusion, and (t(3)) after the end of the reperfusion, in order to determine superoxide dismutase (SOD) and neopterin values. Specimens of the intestine were obtained for histological analysis and determination of malondialdehyde (MDA). RESULTS: In Group A, mucosal lesions were more extensive compared to those of the other three groups. Similarly, MDA, SOD and neopterin values were significantly higher. On the contrary, Group D showed the mildest mucosal lesions, as well as the lowest MDA, SOD and neopterin values. Finally, the lesions and the above mentioned values were bigger in Group C than in Group D. CONCLUSIONS: The administration of allopurinol attenuates the production and damage effect of free oxygen radicals during ischemia reperfusion of the small intestine, thus protecting the intestinal mucosa. Its maximum beneficial action is achieved when administered both before ischemia and before reperfusion of the small intestine.
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spelling pubmed-37464442013-08-19 The role of allopurinol's timing in the ischemia reperfusion injury of small intestine Sapalidis, Konstantinos Papavramidis, Theodossis S Gialamas, Eleftherios Deligiannidis, Nikolaos Tzioufa, Valentini Papavramidis, Spiros J Emerg Trauma Shock Basic Science Research INTRODUCTION: Allopurinol acts protectively in the ischemia reperfusion injury of the small intestine. The aim of this experimental study is to define the ideal time of administration of allopurinol, in experimental models of ischemia/reperfusion. MATERIALS AND METHODS: We used 46 rabbits that were divided into four groups. Group A was the control. In Group B allopurinol was administered 10 min before ischemia and in Group C 2 min before reperfusion. In Group D, allopurinol was administered before ischemia and before reperfusion in half doses. Blood samples were collected at three different moments: (t(1)) prior to ischemia, (t(2)) prior to reperfusion, and (t(3)) after the end of the reperfusion, in order to determine superoxide dismutase (SOD) and neopterin values. Specimens of the intestine were obtained for histological analysis and determination of malondialdehyde (MDA). RESULTS: In Group A, mucosal lesions were more extensive compared to those of the other three groups. Similarly, MDA, SOD and neopterin values were significantly higher. On the contrary, Group D showed the mildest mucosal lesions, as well as the lowest MDA, SOD and neopterin values. Finally, the lesions and the above mentioned values were bigger in Group C than in Group D. CONCLUSIONS: The administration of allopurinol attenuates the production and damage effect of free oxygen radicals during ischemia reperfusion of the small intestine, thus protecting the intestinal mucosa. Its maximum beneficial action is achieved when administered both before ischemia and before reperfusion of the small intestine. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3746444/ /pubmed/23960379 http://dx.doi.org/10.4103/0974-2700.115346 Text en Copyright: © Journal of Emergencies, Trauma, and Shock http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Science Research
Sapalidis, Konstantinos
Papavramidis, Theodossis S
Gialamas, Eleftherios
Deligiannidis, Nikolaos
Tzioufa, Valentini
Papavramidis, Spiros
The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title_full The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title_fullStr The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title_full_unstemmed The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title_short The role of allopurinol's timing in the ischemia reperfusion injury of small intestine
title_sort role of allopurinol's timing in the ischemia reperfusion injury of small intestine
topic Basic Science Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746444/
https://www.ncbi.nlm.nih.gov/pubmed/23960379
http://dx.doi.org/10.4103/0974-2700.115346
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