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The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism

PURPOSE: To investigate the protective effects against ischemia reperfusion injury of dipyridamole in a model of induced priapism in rats. MATERIALS AND METHODS: Twenty-four male Sprague-Dawley rats were divided into four groups, control, P/R, P/R+DMSO and P/R+D. 3ml blood specimens were collected f...

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Autores principales: Karaguzel, Ersagun, Bayraktar, Cemil, Kutlu, Omer, Yulug, Esin, Mentese, Ahmet, Okatan, Ali Ertan, Colak, Fatih, Ozer, Serap, O.Kazaz, Ilke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Urologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811240/
https://www.ncbi.nlm.nih.gov/pubmed/27136481
http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0072
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author Karaguzel, Ersagun
Bayraktar, Cemil
Kutlu, Omer
Yulug, Esin
Mentese, Ahmet
Okatan, Ali Ertan
Colak, Fatih
Ozer, Serap
O.Kazaz, Ilke
author_facet Karaguzel, Ersagun
Bayraktar, Cemil
Kutlu, Omer
Yulug, Esin
Mentese, Ahmet
Okatan, Ali Ertan
Colak, Fatih
Ozer, Serap
O.Kazaz, Ilke
author_sort Karaguzel, Ersagun
collection PubMed
description PURPOSE: To investigate the protective effects against ischemia reperfusion injury of dipyridamole in a model of induced priapism in rats. MATERIALS AND METHODS: Twenty-four male Sprague-Dawley rats were divided into four groups, control, P/R, P/R+DMSO and P/R+D. 3ml blood specimens were collected from vena cava inferior in order to determine serum MDA, IMA, TAS, TOS and OSI values, and penile tissue was taken for histopathological examination in control group. Priapism was induced in P/R group. After 1h, priapism was concluded and 30 min reperfusion was performed. In P/R+DMSO group 1ml/kg DMSO was administered intraperitoneally 30 min before reperfusion, while in P/R+D group 10mg/kg dipyridamole was administered intraperitoneally 30 min before reperfusion. Blood and penis specimens were collected after the end of 30 min reperfusion period. Sinusoidal area (µm(2)), tears in tunica albuginea and injury parameters in sinusoidal endothelium of penis were investigated. RESULTS: Histopathological examination revealed no significant changes in term of sinusoidal area. A decrease in tears was observed in P/R+D group compared to P/R group (p<0.05). Endothelial injury decreased in P/R+D group compared to P/R group (p>0.05). There were no significant differences in MDA and IMA values between groups. A significant increase in TOS and OSI values was observed in P/R+D group compared to P/R group. A significant decrease in TAS levels was observed in P/R+D group compared to the P/R group. CONCLUSIONS: The administration of dipyridamole before reperfusion in ischemic priapism model has a potential protective effect against histopathological injury of the penis.
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spelling pubmed-48112402016-05-09 The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism Karaguzel, Ersagun Bayraktar, Cemil Kutlu, Omer Yulug, Esin Mentese, Ahmet Okatan, Ali Ertan Colak, Fatih Ozer, Serap O.Kazaz, Ilke Int Braz J Urol Original Article PURPOSE: To investigate the protective effects against ischemia reperfusion injury of dipyridamole in a model of induced priapism in rats. MATERIALS AND METHODS: Twenty-four male Sprague-Dawley rats were divided into four groups, control, P/R, P/R+DMSO and P/R+D. 3ml blood specimens were collected from vena cava inferior in order to determine serum MDA, IMA, TAS, TOS and OSI values, and penile tissue was taken for histopathological examination in control group. Priapism was induced in P/R group. After 1h, priapism was concluded and 30 min reperfusion was performed. In P/R+DMSO group 1ml/kg DMSO was administered intraperitoneally 30 min before reperfusion, while in P/R+D group 10mg/kg dipyridamole was administered intraperitoneally 30 min before reperfusion. Blood and penis specimens were collected after the end of 30 min reperfusion period. Sinusoidal area (µm(2)), tears in tunica albuginea and injury parameters in sinusoidal endothelium of penis were investigated. RESULTS: Histopathological examination revealed no significant changes in term of sinusoidal area. A decrease in tears was observed in P/R+D group compared to P/R group (p<0.05). Endothelial injury decreased in P/R+D group compared to P/R group (p>0.05). There were no significant differences in MDA and IMA values between groups. A significant increase in TOS and OSI values was observed in P/R+D group compared to P/R group. A significant decrease in TAS levels was observed in P/R+D group compared to the P/R group. CONCLUSIONS: The administration of dipyridamole before reperfusion in ischemic priapism model has a potential protective effect against histopathological injury of the penis. Sociedade Brasileira de Urologia 2016 /pmc/articles/PMC4811240/ /pubmed/27136481 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0072 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
Karaguzel, Ersagun
Bayraktar, Cemil
Kutlu, Omer
Yulug, Esin
Mentese, Ahmet
Okatan, Ali Ertan
Colak, Fatih
Ozer, Serap
O.Kazaz, Ilke
The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title_full The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title_fullStr The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title_full_unstemmed The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title_short The possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
title_sort possible protective effects of dipyridamole on ischemic reperfusion injury of priapism
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811240/
https://www.ncbi.nlm.nih.gov/pubmed/27136481
http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0072
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