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Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys

OBJECTIVES: Amifostine is a drug which can eliminate free oxygen radicals that appear in the body after radiation or chemotherapeutic agent exposure. It is used to decrease the renal toxicity of cisplatin. The aim of this study was to determine the role of amifostine in warm ischemia kidney model fo...

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Autores principales: Merter, Ayse Arducoglu, Mayir, Burhan, Erdogan, Okan, Colak, Taner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386128/
https://www.ncbi.nlm.nih.gov/pubmed/25878379
http://dx.doi.org/10.4103/0253-7613.153427
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author Merter, Ayse Arducoglu
Mayir, Burhan
Erdogan, Okan
Colak, Taner
author_facet Merter, Ayse Arducoglu
Mayir, Burhan
Erdogan, Okan
Colak, Taner
author_sort Merter, Ayse Arducoglu
collection PubMed
description OBJECTIVES: Amifostine is a drug which can eliminate free oxygen radicals that appear in the body after radiation or chemotherapeutic agent exposure. It is used to decrease the renal toxicity of cisplatin. The aim of this study was to determine the role of amifostine in warm ischemia kidney model for prevention of ischemia/reperfusion injury and also to find out the mechanism for prevention from ischemia/reperfusion injury if such an effect does exist. MATERIALS AND METHODS: Adult female rats (n = 40) that used in our study were divided into three groups. Group 1: Control (n = 8), group 2: Ischemia-control (n = 16), group 3: Amifostine treated (n = 16). The effect of amifostine on ischemia/reperfusion injury investigated in rat kidneys. RESULTS: At the 7(th) day, blood urea nitrogen level was statistically significantly higher in ischemia-control group than all groups (P = 0.001) and mean serum creatinine levels were found to be the highest in ischemia-control group (P = 0.091). Mean malondialdehyde levels in left kidneys removed on the 7(th) day were not significantly different (P = 0.105) at all three groups. Between ischemia-control group and amifostine group, there was a significant difference in reduced glutathione (GSH) levels (P = 0.001). In amifostine group, grade 4 necrosis was not detected neither on 7(th) day nor day 0. CONCLUSION: Amifostine could decrease the degree and severity of necrosis after reperfusion. Amifostine could not prevent membrane lipid peroxidation caused by superoxide anion radicals in kidney but they could protect tissues from the harmful effects of ischemia/reperfusion injury by increasing the level of reduced GSH which is a well-known oxygen radical eliminator.
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spelling pubmed-43861282015-04-15 Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys Merter, Ayse Arducoglu Mayir, Burhan Erdogan, Okan Colak, Taner Indian J Pharmacol Research Article OBJECTIVES: Amifostine is a drug which can eliminate free oxygen radicals that appear in the body after radiation or chemotherapeutic agent exposure. It is used to decrease the renal toxicity of cisplatin. The aim of this study was to determine the role of amifostine in warm ischemia kidney model for prevention of ischemia/reperfusion injury and also to find out the mechanism for prevention from ischemia/reperfusion injury if such an effect does exist. MATERIALS AND METHODS: Adult female rats (n = 40) that used in our study were divided into three groups. Group 1: Control (n = 8), group 2: Ischemia-control (n = 16), group 3: Amifostine treated (n = 16). The effect of amifostine on ischemia/reperfusion injury investigated in rat kidneys. RESULTS: At the 7(th) day, blood urea nitrogen level was statistically significantly higher in ischemia-control group than all groups (P = 0.001) and mean serum creatinine levels were found to be the highest in ischemia-control group (P = 0.091). Mean malondialdehyde levels in left kidneys removed on the 7(th) day were not significantly different (P = 0.105) at all three groups. Between ischemia-control group and amifostine group, there was a significant difference in reduced glutathione (GSH) levels (P = 0.001). In amifostine group, grade 4 necrosis was not detected neither on 7(th) day nor day 0. CONCLUSION: Amifostine could decrease the degree and severity of necrosis after reperfusion. Amifostine could not prevent membrane lipid peroxidation caused by superoxide anion radicals in kidney but they could protect tissues from the harmful effects of ischemia/reperfusion injury by increasing the level of reduced GSH which is a well-known oxygen radical eliminator. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4386128/ /pubmed/25878379 http://dx.doi.org/10.4103/0253-7613.153427 Text en Copyright: © Indian Journal of Pharmacology 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 Research Article
Merter, Ayse Arducoglu
Mayir, Burhan
Erdogan, Okan
Colak, Taner
Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title_full Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title_fullStr Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title_full_unstemmed Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title_short Protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
title_sort protective effects of amifostine on ischemia-reperfusion injury of rat kidneys
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386128/
https://www.ncbi.nlm.nih.gov/pubmed/25878379
http://dx.doi.org/10.4103/0253-7613.153427
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