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Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats
BACKGROUND AND AIM: Allow for protection of briefly ischemic tissues against the harmful effects of subsequent prolonged ischemia is a phenomennon called as Ischemic Preconditioning (IP). IP has not been studied in ischemia-reperfusion (I/R) model of peripheral nerve before. We aimed to study the ef...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636295/ https://www.ncbi.nlm.nih.gov/pubmed/17147773 http://dx.doi.org/10.1186/1749-7221-1-2 |
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author | Coban, Yusuf Kenan Ciralik, Harun Kurutas, Ergul Belge |
author_facet | Coban, Yusuf Kenan Ciralik, Harun Kurutas, Ergul Belge |
author_sort | Coban, Yusuf Kenan |
collection | PubMed |
description | BACKGROUND AND AIM: Allow for protection of briefly ischemic tissues against the harmful effects of subsequent prolonged ischemia is a phenomennon called as Ischemic Preconditioning (IP). IP has not been studied in ischemia-reperfusion (I/R) model of peripheral nerve before. We aimed to study the effects of acute IP on I/R injury of peripheral nerve in rats. METHOD: 70 adult male rats were randomly divided into 5 groups in part 1 experimentation and 3 groups in part 2 experimentation. A rat model of severe nerve ischemia which was produced by tying iliac arteries and all idenfiable anastomotic vessels with a silk suture (6-0) was used to study the effects of I/R and IP on nerve biochemistry. The suture technique used was a slip-knot technique for rapid release at time of reperfusion in the study. Cytoplasmic vacuolar degeneration was also histopathologically evaluated by light microscopic examination in sciatic nerves of rats at 7th day in part 2 study. RESULTS: 3 hours of Reperfusion resulted in an increase in nerve malondialdehyde levels when compared with ischemia and non-ischemia groups (p < 0.001 and p < 0.0001 respectively). IP had significantly lower nerve MDA levels than 3 h reperfusion group (p < 0.001). The differences between ischemic, IP and non-ischemic control groups were not significant (p > 0.05). There was also a significant decrease in vacoular degeneration of sciatic nerves in IP group than I/R group (p < 0.05). CONCLUSION: IP reduces the severity of I/R injury in peripheral nerve as shown by reduced tissue MDA levels at 3 th hour of reperfusion and axonal vacoulization at 7 th postischemic day. |
format | Text |
id | pubmed-1636295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16362952006-11-29 Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats Coban, Yusuf Kenan Ciralik, Harun Kurutas, Ergul Belge J Brachial Plex Peripher Nerve Inj Research Article BACKGROUND AND AIM: Allow for protection of briefly ischemic tissues against the harmful effects of subsequent prolonged ischemia is a phenomennon called as Ischemic Preconditioning (IP). IP has not been studied in ischemia-reperfusion (I/R) model of peripheral nerve before. We aimed to study the effects of acute IP on I/R injury of peripheral nerve in rats. METHOD: 70 adult male rats were randomly divided into 5 groups in part 1 experimentation and 3 groups in part 2 experimentation. A rat model of severe nerve ischemia which was produced by tying iliac arteries and all idenfiable anastomotic vessels with a silk suture (6-0) was used to study the effects of I/R and IP on nerve biochemistry. The suture technique used was a slip-knot technique for rapid release at time of reperfusion in the study. Cytoplasmic vacuolar degeneration was also histopathologically evaluated by light microscopic examination in sciatic nerves of rats at 7th day in part 2 study. RESULTS: 3 hours of Reperfusion resulted in an increase in nerve malondialdehyde levels when compared with ischemia and non-ischemia groups (p < 0.001 and p < 0.0001 respectively). IP had significantly lower nerve MDA levels than 3 h reperfusion group (p < 0.001). The differences between ischemic, IP and non-ischemic control groups were not significant (p > 0.05). There was also a significant decrease in vacoular degeneration of sciatic nerves in IP group than I/R group (p < 0.05). CONCLUSION: IP reduces the severity of I/R injury in peripheral nerve as shown by reduced tissue MDA levels at 3 th hour of reperfusion and axonal vacoulization at 7 th postischemic day. BioMed Central 2006-09-29 /pmc/articles/PMC1636295/ /pubmed/17147773 http://dx.doi.org/10.1186/1749-7221-1-2 Text en Copyright © 2006 Coban et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Coban, Yusuf Kenan Ciralik, Harun Kurutas, Ergul Belge Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title | Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title_full | Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title_fullStr | Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title_full_unstemmed | Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title_short | Ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
title_sort | ischemic preconditioning reduces the severity of ischemia-reperfusion injury of peripheral nerve in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636295/ https://www.ncbi.nlm.nih.gov/pubmed/17147773 http://dx.doi.org/10.1186/1749-7221-1-2 |
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