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Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction

INTRODUCTION/OBJECTIVE: Ureteral obstruction is a common pathology and causes kidney fibrosis and dysfunction at late period. In this present study, we investigated the antifibrotic and antiinflammatory effects of hydrogen sulfide on kidney damage after unilateral ureteral obstruction (UUO) in rats....

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Autores principales: Dursun, Murat, Otunctemur, Alper, Ozbek, Emin, Sahin, Suleyman, Besiroglu, Huseyin, Ozsoy, Ozgur Doga, Cekmen, Mustafa, Somay, Adnan, Ozbay, Nurver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756947/
https://www.ncbi.nlm.nih.gov/pubmed/26742979
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0090
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author Dursun, Murat
Otunctemur, Alper
Ozbek, Emin
Sahin, Suleyman
Besiroglu, Huseyin
Ozsoy, Ozgur Doga
Cekmen, Mustafa
Somay, Adnan
Ozbay, Nurver
author_facet Dursun, Murat
Otunctemur, Alper
Ozbek, Emin
Sahin, Suleyman
Besiroglu, Huseyin
Ozsoy, Ozgur Doga
Cekmen, Mustafa
Somay, Adnan
Ozbay, Nurver
author_sort Dursun, Murat
collection PubMed
description INTRODUCTION/OBJECTIVE: Ureteral obstruction is a common pathology and causes kidney fibrosis and dysfunction at late period. In this present study, we investigated the antifibrotic and antiinflammatory effects of hydrogen sulfide on kidney damage after unilateral ureteral obstruction (UUO) in rats. MATERIALS AND METHODS: 24 rats were divided into four groups. Group 1 was control, group 2 was sham, group 3 included rats with UUO and group 4 rats with UUO which were given sodium hydrogen sulfide (NaHS)-exogenous donor of hydrogen sulfide (intraperitoneally 56μmoL/kg/day). After 14 days, rats were killed and their kidneys were taken and blood analysis was performed. Tubular necrosis, mononuclear cell infiltration and interstitial fibrosis were determined histopathologically in a part of the kidneys; nitric oxide (NO), malondialdehyde (MDA) and reduced glutathione (GSH) levels were determined in the other part of the kidneys. Urea-creatinine levels were investigated by blood analysis. Statistical analyses were made by the Chi-square test and one-way analysis of variance (ANOVA). RESULTS: There was no significantly difference for urea-creatinine levels among groups. Pathologically, there was serious tubular necrosis and fibrosis in group 3 and there was significantly decreasing of tubular necrosis and fibrosis in group 4 (p<0.005). Also, there was significantly increase of NO and MDA levels and decrease of GSH levels in group 3 compared to other groups (p<0.005). CONCLUSIONS: hydrogen sulfide prevents kidney damage with antioxidant and antiinflammatory effect.
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spelling pubmed-47569472016-05-09 Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction Dursun, Murat Otunctemur, Alper Ozbek, Emin Sahin, Suleyman Besiroglu, Huseyin Ozsoy, Ozgur Doga Cekmen, Mustafa Somay, Adnan Ozbay, Nurver Int Braz J Urol Original Article INTRODUCTION/OBJECTIVE: Ureteral obstruction is a common pathology and causes kidney fibrosis and dysfunction at late period. In this present study, we investigated the antifibrotic and antiinflammatory effects of hydrogen sulfide on kidney damage after unilateral ureteral obstruction (UUO) in rats. MATERIALS AND METHODS: 24 rats were divided into four groups. Group 1 was control, group 2 was sham, group 3 included rats with UUO and group 4 rats with UUO which were given sodium hydrogen sulfide (NaHS)-exogenous donor of hydrogen sulfide (intraperitoneally 56μmoL/kg/day). After 14 days, rats were killed and their kidneys were taken and blood analysis was performed. Tubular necrosis, mononuclear cell infiltration and interstitial fibrosis were determined histopathologically in a part of the kidneys; nitric oxide (NO), malondialdehyde (MDA) and reduced glutathione (GSH) levels were determined in the other part of the kidneys. Urea-creatinine levels were investigated by blood analysis. Statistical analyses were made by the Chi-square test and one-way analysis of variance (ANOVA). RESULTS: There was no significantly difference for urea-creatinine levels among groups. Pathologically, there was serious tubular necrosis and fibrosis in group 3 and there was significantly decreasing of tubular necrosis and fibrosis in group 4 (p<0.005). Also, there was significantly increase of NO and MDA levels and decrease of GSH levels in group 3 compared to other groups (p<0.005). CONCLUSIONS: hydrogen sulfide prevents kidney damage with antioxidant and antiinflammatory effect. Sociedade Brasileira de Urologia 2015 /pmc/articles/PMC4756947/ /pubmed/26742979 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0090 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dursun, Murat
Otunctemur, Alper
Ozbek, Emin
Sahin, Suleyman
Besiroglu, Huseyin
Ozsoy, Ozgur Doga
Cekmen, Mustafa
Somay, Adnan
Ozbay, Nurver
Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title_full Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title_fullStr Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title_full_unstemmed Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title_short Protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
title_sort protective effect of hydrogen sulfide on renal injury in the experimental unilateral ureteral obstruction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756947/
https://www.ncbi.nlm.nih.gov/pubmed/26742979
http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0090
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