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Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion

Testicular torsion-detorsion results in enhanced formation of free radicals which contribute to the pathophysiology of testicular tissue damage. Recent reports have identified protective role of pentoxifylline (PTX) against free radicals. Thus, we determined the protective effect of pentoxifylline a...

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Autores principales: Dhulqarnain, Akanji Omotosho, Takzaree, Nasrin, Hassanzadeh, Golamreza, Tooli, Heidar, Malekzadeh, Mehrnoush, Khanmohammadi, Nasrin, Yaghobinejad, Mahsa, Solhjoo, Somayeh, Rastegar, Tayebeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8095127/
https://www.ncbi.nlm.nih.gov/pubmed/33997400
http://dx.doi.org/10.1016/j.heliyon.2021.e06868
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author Dhulqarnain, Akanji Omotosho
Takzaree, Nasrin
Hassanzadeh, Golamreza
Tooli, Heidar
Malekzadeh, Mehrnoush
Khanmohammadi, Nasrin
Yaghobinejad, Mahsa
Solhjoo, Somayeh
Rastegar, Tayebeh
author_facet Dhulqarnain, Akanji Omotosho
Takzaree, Nasrin
Hassanzadeh, Golamreza
Tooli, Heidar
Malekzadeh, Mehrnoush
Khanmohammadi, Nasrin
Yaghobinejad, Mahsa
Solhjoo, Somayeh
Rastegar, Tayebeh
author_sort Dhulqarnain, Akanji Omotosho
collection PubMed
description Testicular torsion-detorsion results in enhanced formation of free radicals which contribute to the pathophysiology of testicular tissue damage. Recent reports have identified protective role of pentoxifylline (PTX) against free radicals. Thus, we determined the protective effect of pentoxifylline against testicular damage in mouse model of testicular torsion-detorsion. Twenty (6 weeks old) male mice were divided into 4 groups of 5 animals each namely: Control (sham operated group), T1 (Torsion-detosion + single dose 100 mg/kg PTX, T2 (torsion-detorsion + 20 mg/kg PTX for 2 weeks and T/D (torsion-detorsion only). Animals in T1, T2 and T/D groups underwent 2 h of testicular torsion with the left testes rotated 720° (clockwisely) followed by 30 min of detorsion. After detorsion, drug administration was done intraperitoneally. The left testes of all the animals were excised on the 35th day after torsion-detortion for histopathological and biochemical assay. Histomorphological analysis of the seminiferous tubules showed that there were significant increase (P < 0.01 or 0.05) in the mean seminiferous tubule diameter, Johnson score and germ cells of animals in Control and T1 compared to T2 and T/D with no significant difference (P > 0.05) in testes weight, sertoli, leydig and myoid cells in all groups. IHC results showed significant increase (P < 0.01 or 0.05) in id4 and scp3 protein markers in Control, T1 and T2 compared to T/D. Oxidative stress analysis revealed that Pentoxifylline significantly increased (P < 0.01 or 0.05) the level of SOD, catalase, mRNA expression of akt and pi3k genes but significantly suppress (P < 0.01 or 0.05) MDA and Caspase-3 level in Control, T1 and T2 compared to T/D. Pentoxifylline could be used as an adjunct therapy to surgery in the treatment of torsion-detorsion related testicular injury, However, Further studies are needed to evaluate the effects of pentoxifylline on testicular torsion.
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spelling pubmed-80951272021-05-13 Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion Dhulqarnain, Akanji Omotosho Takzaree, Nasrin Hassanzadeh, Golamreza Tooli, Heidar Malekzadeh, Mehrnoush Khanmohammadi, Nasrin Yaghobinejad, Mahsa Solhjoo, Somayeh Rastegar, Tayebeh Heliyon Research Article Testicular torsion-detorsion results in enhanced formation of free radicals which contribute to the pathophysiology of testicular tissue damage. Recent reports have identified protective role of pentoxifylline (PTX) against free radicals. Thus, we determined the protective effect of pentoxifylline against testicular damage in mouse model of testicular torsion-detorsion. Twenty (6 weeks old) male mice were divided into 4 groups of 5 animals each namely: Control (sham operated group), T1 (Torsion-detosion + single dose 100 mg/kg PTX, T2 (torsion-detorsion + 20 mg/kg PTX for 2 weeks and T/D (torsion-detorsion only). Animals in T1, T2 and T/D groups underwent 2 h of testicular torsion with the left testes rotated 720° (clockwisely) followed by 30 min of detorsion. After detorsion, drug administration was done intraperitoneally. The left testes of all the animals were excised on the 35th day after torsion-detortion for histopathological and biochemical assay. Histomorphological analysis of the seminiferous tubules showed that there were significant increase (P < 0.01 or 0.05) in the mean seminiferous tubule diameter, Johnson score and germ cells of animals in Control and T1 compared to T2 and T/D with no significant difference (P > 0.05) in testes weight, sertoli, leydig and myoid cells in all groups. IHC results showed significant increase (P < 0.01 or 0.05) in id4 and scp3 protein markers in Control, T1 and T2 compared to T/D. Oxidative stress analysis revealed that Pentoxifylline significantly increased (P < 0.01 or 0.05) the level of SOD, catalase, mRNA expression of akt and pi3k genes but significantly suppress (P < 0.01 or 0.05) MDA and Caspase-3 level in Control, T1 and T2 compared to T/D. Pentoxifylline could be used as an adjunct therapy to surgery in the treatment of torsion-detorsion related testicular injury, However, Further studies are needed to evaluate the effects of pentoxifylline on testicular torsion. Elsevier 2021-04-23 /pmc/articles/PMC8095127/ /pubmed/33997400 http://dx.doi.org/10.1016/j.heliyon.2021.e06868 Text en © 2021 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Dhulqarnain, Akanji Omotosho
Takzaree, Nasrin
Hassanzadeh, Golamreza
Tooli, Heidar
Malekzadeh, Mehrnoush
Khanmohammadi, Nasrin
Yaghobinejad, Mahsa
Solhjoo, Somayeh
Rastegar, Tayebeh
Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title_full Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title_fullStr Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title_full_unstemmed Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title_short Pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of PI3K/AKT pathway in mouse model of testicular torsion-detorsion
title_sort pentoxifylline improves the survival of spermatogenic cells via oxidative stress suppression and upregulation of pi3k/akt pathway in mouse model of testicular torsion-detorsion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8095127/
https://www.ncbi.nlm.nih.gov/pubmed/33997400
http://dx.doi.org/10.1016/j.heliyon.2021.e06868
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