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Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats
OBJECTIVE: Acute mesenteric ischaemia leads to intestinal damage. Restoration of blood flow results in further damage to tissue, which is called reperfusion injury. This study aimed to investigate the protective effects of short-interval postconditioning and to determine the optimal interval for rep...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536428/ https://www.ncbi.nlm.nih.gov/pubmed/28553765 http://dx.doi.org/10.1177/0300060517708921 |
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author | Ozkisacik, Sezen Erdem, Ali Onur Etensel, Barlas Tataroglu, Canten Serter, Mukadder Yazici, Mesut |
author_facet | Ozkisacik, Sezen Erdem, Ali Onur Etensel, Barlas Tataroglu, Canten Serter, Mukadder Yazici, Mesut |
author_sort | Ozkisacik, Sezen |
collection | PubMed |
description | OBJECTIVE: Acute mesenteric ischaemia leads to intestinal damage. Restoration of blood flow results in further damage to tissue, which is called reperfusion injury. This study aimed to investigate the protective effects of short-interval postconditioning and to determine the optimal interval for reperfusion in an experimental rat model of intestinal ischaemia. METHODS: Forty adult male Wistar rats were grouped as follows: sham (Sh), ischaemia + reperfusion (IR), ischaemia + postconditioning for 5 seconds (PC5), ischaemia + postconditioning for 10 seconds (PC10), and ischaemia + postconditioning for 20 seconds (PC20). For postconditioning, 10 cycles of reperfusion (5, 10, or 20 seconds) interspersed by 10 cycles of 10 seconds of ischaemia were performed. Blood glutathione reductase (GR) and glutathione peroxidase (GPx) levels were measured. Intestinal tissue damage was assessed histopathologically. RESULTS: GR levels were significantly higher in the PC5 group than in the IR group (37.7 ± 9.0 vs. 18.5 ± 2.0 min/g Hb). GPx levels were significantly higher in the PC10 group than in the IR group (43.2 ± 9.2 vs. 15.9 ± 4.6 U/g Hb). The histopathological score was significantly lower in the PC5 group (1.1 ± 0.1) than in the IR group (2.1 ± 0.2). CONCLUSION: Short-interval postconditioning reduces reperfusion injury in the ischaemic bowel and the optimal interval for reperfusion is 5 seconds. The long-term effects of short-interval postconditioning and the optimal reperfusion interval in intestinal ischaemia–reperfusion in rats need to be investigated. |
format | Online Article Text |
id | pubmed-5536428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-55364282017-10-03 Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats Ozkisacik, Sezen Erdem, Ali Onur Etensel, Barlas Tataroglu, Canten Serter, Mukadder Yazici, Mesut J Int Med Res Research Reports OBJECTIVE: Acute mesenteric ischaemia leads to intestinal damage. Restoration of blood flow results in further damage to tissue, which is called reperfusion injury. This study aimed to investigate the protective effects of short-interval postconditioning and to determine the optimal interval for reperfusion in an experimental rat model of intestinal ischaemia. METHODS: Forty adult male Wistar rats were grouped as follows: sham (Sh), ischaemia + reperfusion (IR), ischaemia + postconditioning for 5 seconds (PC5), ischaemia + postconditioning for 10 seconds (PC10), and ischaemia + postconditioning for 20 seconds (PC20). For postconditioning, 10 cycles of reperfusion (5, 10, or 20 seconds) interspersed by 10 cycles of 10 seconds of ischaemia were performed. Blood glutathione reductase (GR) and glutathione peroxidase (GPx) levels were measured. Intestinal tissue damage was assessed histopathologically. RESULTS: GR levels were significantly higher in the PC5 group than in the IR group (37.7 ± 9.0 vs. 18.5 ± 2.0 min/g Hb). GPx levels were significantly higher in the PC10 group than in the IR group (43.2 ± 9.2 vs. 15.9 ± 4.6 U/g Hb). The histopathological score was significantly lower in the PC5 group (1.1 ± 0.1) than in the IR group (2.1 ± 0.2). CONCLUSION: Short-interval postconditioning reduces reperfusion injury in the ischaemic bowel and the optimal interval for reperfusion is 5 seconds. The long-term effects of short-interval postconditioning and the optimal reperfusion interval in intestinal ischaemia–reperfusion in rats need to be investigated. SAGE Publications 2017-05-28 2017-06 /pmc/articles/PMC5536428/ /pubmed/28553765 http://dx.doi.org/10.1177/0300060517708921 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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 | Research Reports Ozkisacik, Sezen Erdem, Ali Onur Etensel, Barlas Tataroglu, Canten Serter, Mukadder Yazici, Mesut Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title | Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title_full | Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title_fullStr | Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title_full_unstemmed | Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title_short | Short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
title_sort | short-interval postconditioning protects the bowel against ischaemia–reperfusion injury in rats |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536428/ https://www.ncbi.nlm.nih.gov/pubmed/28553765 http://dx.doi.org/10.1177/0300060517708921 |
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