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The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study

OBJECTIVE: Contrast-induced nephropathy (CIN) is one of the most common causes of acute renal failure in hospitalized patients. The direct toxic effect of contrast media; ischemic damage caused by reactive oxygen species; increased perivascular hydrostatic pressure; high viscosity and changes in the...

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Autores principales: Özbek, Kerem, Ceyhan, Köksal, Koç, Fatih, Söğüt, Erkan, Altunkaş, Fatih, Karayakalı, Metin, Çelik, Ataç, Kadı, Hasan, Köseoğlu, R. Doğan, Önalan, Orhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336839/
https://www.ncbi.nlm.nih.gov/pubmed/25880289
http://dx.doi.org/10.5152/akd.2014.5380
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author Özbek, Kerem
Ceyhan, Köksal
Koç, Fatih
Söğüt, Erkan
Altunkaş, Fatih
Karayakalı, Metin
Çelik, Ataç
Kadı, Hasan
Köseoğlu, R. Doğan
Önalan, Orhan
author_facet Özbek, Kerem
Ceyhan, Köksal
Koç, Fatih
Söğüt, Erkan
Altunkaş, Fatih
Karayakalı, Metin
Çelik, Ataç
Kadı, Hasan
Köseoğlu, R. Doğan
Önalan, Orhan
author_sort Özbek, Kerem
collection PubMed
description OBJECTIVE: Contrast-induced nephropathy (CIN) is one of the most common causes of acute renal failure in hospitalized patients. The direct toxic effect of contrast media; ischemic damage caused by reactive oxygen species; increased perivascular hydrostatic pressure; high viscosity and changes in the activity of vasoactive substances play important roles in the pathogenesis. Tadalafil inhibits the phosphodiesterase enzyme which destroys nitric oxide. Nitric oxide causes renal vasodilatation, increases renal medullar blood flow and mediates the removal of free oxygen radicals. Drugs that increase levels of nitric oxide are expected to reduce the development of contrast nephropathy due to contrast media. We aimed to test the hypothesis that tadalafil reduces the development of contrast nephropathy due to contrast toxicity. METHODS: A total of 24 female Wistar albino rats, three groups of eight, were included in the study. After 48 hours of dehydration, contrast media (meglumine diatrozoate, 6 mL/kg) was administered to the first group, and contrast media with tadalafil (10 mg/kg) was administered to the second group. The third group served as the control group. Blood and tissue samples were taken 48 hours after this procedure. RESULTS: Serum cystatin C, serum creatinine and blood urea nitrogen (BUN) values were significantly lower in the contrast with tadalafil group compared to the group given only contrast. Serum and tissue malondialdehyde (MDA) levels were significantly lower in the contrast with tadalafil group than in the contrast only group. CONCLUSION: These results demonstrate the protective effect of tadalafil in the prevention of CIN in rats.
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spelling pubmed-53368392017-06-28 The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study Özbek, Kerem Ceyhan, Köksal Koç, Fatih Söğüt, Erkan Altunkaş, Fatih Karayakalı, Metin Çelik, Ataç Kadı, Hasan Köseoğlu, R. Doğan Önalan, Orhan Anatol J Cardiol Original Investigation OBJECTIVE: Contrast-induced nephropathy (CIN) is one of the most common causes of acute renal failure in hospitalized patients. The direct toxic effect of contrast media; ischemic damage caused by reactive oxygen species; increased perivascular hydrostatic pressure; high viscosity and changes in the activity of vasoactive substances play important roles in the pathogenesis. Tadalafil inhibits the phosphodiesterase enzyme which destroys nitric oxide. Nitric oxide causes renal vasodilatation, increases renal medullar blood flow and mediates the removal of free oxygen radicals. Drugs that increase levels of nitric oxide are expected to reduce the development of contrast nephropathy due to contrast media. We aimed to test the hypothesis that tadalafil reduces the development of contrast nephropathy due to contrast toxicity. METHODS: A total of 24 female Wistar albino rats, three groups of eight, were included in the study. After 48 hours of dehydration, contrast media (meglumine diatrozoate, 6 mL/kg) was administered to the first group, and contrast media with tadalafil (10 mg/kg) was administered to the second group. The third group served as the control group. Blood and tissue samples were taken 48 hours after this procedure. RESULTS: Serum cystatin C, serum creatinine and blood urea nitrogen (BUN) values were significantly lower in the contrast with tadalafil group compared to the group given only contrast. Serum and tissue malondialdehyde (MDA) levels were significantly lower in the contrast with tadalafil group than in the contrast only group. CONCLUSION: These results demonstrate the protective effect of tadalafil in the prevention of CIN in rats. Kare Publishing 2015-04 2014-04-16 /pmc/articles/PMC5336839/ /pubmed/25880289 http://dx.doi.org/10.5152/akd.2014.5380 Text en Copyright © 2016 Turkish Society of Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Original Investigation
Özbek, Kerem
Ceyhan, Köksal
Koç, Fatih
Söğüt, Erkan
Altunkaş, Fatih
Karayakalı, Metin
Çelik, Ataç
Kadı, Hasan
Köseoğlu, R. Doğan
Önalan, Orhan
The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title_full The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title_fullStr The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title_full_unstemmed The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title_short The protective effect of single dose tadalafil in contrast-induced nephropathy: An experimental study
title_sort protective effect of single dose tadalafil in contrast-induced nephropathy: an experimental study
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336839/
https://www.ncbi.nlm.nih.gov/pubmed/25880289
http://dx.doi.org/10.5152/akd.2014.5380
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