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Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model
OBJECTIVES: To evaluate protective effects of darbepoetin and tadalafil against ischemia-reperfusion injury in ipsilateral and contralateral testicle. MATERIALS AND METHODS: Thirty 3-month-old adult male Wistar-Albino rats were randomly divided into 5 groups (A-E). Sham operation was performed in th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237536/ https://www.ncbi.nlm.nih.gov/pubmed/30130015 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0200 |
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author | Yildirim, Caglar Yuksel, Ozgur H. Urkmez, Ahmet Sahin, Aytac Somay, Adnan Verit, Ayhan |
author_facet | Yildirim, Caglar Yuksel, Ozgur H. Urkmez, Ahmet Sahin, Aytac Somay, Adnan Verit, Ayhan |
author_sort | Yildirim, Caglar |
collection | PubMed |
description | OBJECTIVES: To evaluate protective effects of darbepoetin and tadalafil against ischemia-reperfusion injury in ipsilateral and contralateral testicle. MATERIALS AND METHODS: Thirty 3-month-old adult male Wistar-Albino rats were randomly divided into 5 groups (A-E). Sham operation was performed in the first group. In Group B, rats did not received any medication after creating 720 degrees torsion of the left testis. The rats in Group C, D and E received darbepoetin, tadalafil, and darbepoetin/tadalafil combination 30 minutes after creating 720 degrees torsion of the left testis, respectively. The testes of rats in these three groups were detorsioned at 90 minutes after drug administration. Both testes were removed at 30 minutes after detorsion. RESULTS: There were significant differences between the groups in terms of the degree of histopathological damage, Johnsen score, fibrosis score and caspase-3 immunoreactivity in the torsioned testes (p: 0.000). The results for each parameter in the left testes were significantly better in the darbepoetin / tadalafil combination group. Similarly, there were also significant differences in the contralateral testes (p: 0.000). CONCLUSION: The active substances darbepoetin and tadalafil that were used as a combination had protective effects on both testes and produced out better results in preserving testicular histology. Especially in cases where it is not possible to rescue the torsioned testis, this result was more noticeable in the contralateral testis. |
format | Online Article Text |
id | pubmed-6237536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-62375362018-11-19 Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model Yildirim, Caglar Yuksel, Ozgur H. Urkmez, Ahmet Sahin, Aytac Somay, Adnan Verit, Ayhan Int Braz J Urol Original Article OBJECTIVES: To evaluate protective effects of darbepoetin and tadalafil against ischemia-reperfusion injury in ipsilateral and contralateral testicle. MATERIALS AND METHODS: Thirty 3-month-old adult male Wistar-Albino rats were randomly divided into 5 groups (A-E). Sham operation was performed in the first group. In Group B, rats did not received any medication after creating 720 degrees torsion of the left testis. The rats in Group C, D and E received darbepoetin, tadalafil, and darbepoetin/tadalafil combination 30 minutes after creating 720 degrees torsion of the left testis, respectively. The testes of rats in these three groups were detorsioned at 90 minutes after drug administration. Both testes were removed at 30 minutes after detorsion. RESULTS: There were significant differences between the groups in terms of the degree of histopathological damage, Johnsen score, fibrosis score and caspase-3 immunoreactivity in the torsioned testes (p: 0.000). The results for each parameter in the left testes were significantly better in the darbepoetin / tadalafil combination group. Similarly, there were also significant differences in the contralateral testes (p: 0.000). CONCLUSION: The active substances darbepoetin and tadalafil that were used as a combination had protective effects on both testes and produced out better results in preserving testicular histology. Especially in cases where it is not possible to rescue the torsioned testis, this result was more noticeable in the contralateral testis. Sociedade Brasileira de Urologia 2018 /pmc/articles/PMC6237536/ /pubmed/30130015 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0200 Text en https://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 Yildirim, Caglar Yuksel, Ozgur H. Urkmez, Ahmet Sahin, Aytac Somay, Adnan Verit, Ayhan Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title | Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title_full | Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title_fullStr | Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title_full_unstemmed | Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title_short | Protective effects of Tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
title_sort | protective effects of tadalafil and darbepoetin against ischemia - reperfusion injury in a rat testicular torsion model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237536/ https://www.ncbi.nlm.nih.gov/pubmed/30130015 http://dx.doi.org/10.1590/S1677-5538.IBJU.2018.0200 |
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