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Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity

Introduction: Renal dysfunction is caused by ischemia-reperfusion (I/R) injury, which is a common problem in kidney surgery or kidney transplantation. The human body consists of enormous complex antioxidant systems, which inquires adequate selenium (Se) absorption for normal physiologic function. It...

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Autores principales: Hasanvand, Amin, Abbaszadeh, Abolfazl, Darabi, Saeideh, Nazari, Afshin, Gholami, Mohammadreza, Kharazmkia, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nickan Research Institute 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423291/
https://www.ncbi.nlm.nih.gov/pubmed/28497082
http://dx.doi.org/10.15171/jrip.2017.18
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author Hasanvand, Amin
Abbaszadeh, Abolfazl
Darabi, Saeideh
Nazari, Afshin
Gholami, Mohammadreza
Kharazmkia, Ali
author_facet Hasanvand, Amin
Abbaszadeh, Abolfazl
Darabi, Saeideh
Nazari, Afshin
Gholami, Mohammadreza
Kharazmkia, Ali
author_sort Hasanvand, Amin
collection PubMed
description Introduction: Renal dysfunction is caused by ischemia-reperfusion (I/R) injury, which is a common problem in kidney surgery or kidney transplantation. The human body consists of enormous complex antioxidant systems, which inquires adequate selenium (Se) absorption for normal physiologic function. It is known that Se has some antioxidant effects. Objectives: In the present research, effects of the Se on damages caused by I/R injury investigated. Materials and Methods: In this experimental research, four groups of rats (weighing 220±10 g) used, include control group, I/R group, healthy group treated with Se for two weeks, and I/R group with two-week Se treatment. On the test day, I/R was treated in both right and left renal arteries for 45 minutes and the reperfusion was done for 24 hours. Results: In I/R group, the amount of urea and serum creatinine (Cr) was an injury indicator of the kidney cells which showed a significant increase compared with the control group. When the treatment with Se significantly reduced these indicators, glutathione (GSH) enzyme levels reduced significantly in the second group and the enzyme levels increased due to Se treatment in the fourth group. Furthermore, malondialdehyde (MDA) enzyme levels increased in I/R group due to the Se treatment in the fourth group which was significantly reduced. In addition, the tissue damage was reduced in the fourth group compared with I/R group. Conclusion: Se has a protective effect against the I/R injury. This effect might be due to the antioxidant properties of Se.
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spelling pubmed-54232912017-05-11 Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity Hasanvand, Amin Abbaszadeh, Abolfazl Darabi, Saeideh Nazari, Afshin Gholami, Mohammadreza Kharazmkia, Ali J Renal Inj Prev Original Article Introduction: Renal dysfunction is caused by ischemia-reperfusion (I/R) injury, which is a common problem in kidney surgery or kidney transplantation. The human body consists of enormous complex antioxidant systems, which inquires adequate selenium (Se) absorption for normal physiologic function. It is known that Se has some antioxidant effects. Objectives: In the present research, effects of the Se on damages caused by I/R injury investigated. Materials and Methods: In this experimental research, four groups of rats (weighing 220±10 g) used, include control group, I/R group, healthy group treated with Se for two weeks, and I/R group with two-week Se treatment. On the test day, I/R was treated in both right and left renal arteries for 45 minutes and the reperfusion was done for 24 hours. Results: In I/R group, the amount of urea and serum creatinine (Cr) was an injury indicator of the kidney cells which showed a significant increase compared with the control group. When the treatment with Se significantly reduced these indicators, glutathione (GSH) enzyme levels reduced significantly in the second group and the enzyme levels increased due to Se treatment in the fourth group. Furthermore, malondialdehyde (MDA) enzyme levels increased in I/R group due to the Se treatment in the fourth group which was significantly reduced. In addition, the tissue damage was reduced in the fourth group compared with I/R group. Conclusion: Se has a protective effect against the I/R injury. This effect might be due to the antioxidant properties of Se. Nickan Research Institute 2016-11-24 /pmc/articles/PMC5423291/ /pubmed/28497082 http://dx.doi.org/10.15171/jrip.2017.18 Text en Copyright © 2017 The Author(s); Published by Nickan Research Institute http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hasanvand, Amin
Abbaszadeh, Abolfazl
Darabi, Saeideh
Nazari, Afshin
Gholami, Mohammadreza
Kharazmkia, Ali
Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title_full Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title_fullStr Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title_full_unstemmed Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title_short Evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
title_sort evaluation of selenium on kidney function following ischemic injury in rats; protective effects and antioxidant activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423291/
https://www.ncbi.nlm.nih.gov/pubmed/28497082
http://dx.doi.org/10.15171/jrip.2017.18
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