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Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion

BACKGROUND: Testicular torsion (TT) is an acute inflammatory process leading to male infertility. Today, anti‐inflammatory effects of exosomes derived from blood serum are used in various laboratory procedures. In the present study, the anti‐inflammatory effects of blood‐serum‐derived exosomes in tr...

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Autores principales: Keivan, Mona, Mansouri Torghabeh, Fatemeh, Davoodi, Samira, Moradi Maryamneghari, Shima, Dadfar, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434569/
https://www.ncbi.nlm.nih.gov/pubmed/35593125
http://dx.doi.org/10.1002/ame2.12232
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author Keivan, Mona
Mansouri Torghabeh, Fatemeh
Davoodi, Samira
Moradi Maryamneghari, Shima
Dadfar, Reza
author_facet Keivan, Mona
Mansouri Torghabeh, Fatemeh
Davoodi, Samira
Moradi Maryamneghari, Shima
Dadfar, Reza
author_sort Keivan, Mona
collection PubMed
description BACKGROUND: Testicular torsion (TT) is an acute inflammatory process leading to male infertility. Today, anti‐inflammatory effects of exosomes derived from blood serum are used in various laboratory procedures. In the present study, the anti‐inflammatory effects of blood‐serum‐derived exosomes in treatment of acute inflammation following TT in mice were evaluated. MATERIALS AND METHODS: Eighteen male mice were grouped as healthy control, TT, and TT + exosome. TT was induced surgically, and exosomes were extracted from blood serum and administrated by a single intratesticular injection (10 IU). Malondialdehyde (MDA) and Griess assays were used to evaluate the level of oxidative stress. Sperm indices, testosterone (Tes), and apoptotic gene expression (p‐53, Bcl2, and Caspase‐3) were also assessed. H&E and immunohistochemistry (IHC) stainings were used for histopathological investigations. Data analysis was applied by SPSS (v.19) software. RESULTS: Oxidative stress and apoptotic genes expression were increased significantly (p < 0.05) in TT group compared with control. Sperm parameters and Tes were significantly increased, and expression of apoptotic genes was significantly reduced in TT + exosome group (p < 0.05). CONCLUSION: Since the blood‐serum‐derived exosomes have anti‐inflammatory features, the intratesticular application of blood‐serum‐derived exosomes can be used clinically in acute phase of orchitis following TT to inhibit testicular inflammation.
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spelling pubmed-94345692022-09-08 Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion Keivan, Mona Mansouri Torghabeh, Fatemeh Davoodi, Samira Moradi Maryamneghari, Shima Dadfar, Reza Animal Model Exp Med Regular Articles BACKGROUND: Testicular torsion (TT) is an acute inflammatory process leading to male infertility. Today, anti‐inflammatory effects of exosomes derived from blood serum are used in various laboratory procedures. In the present study, the anti‐inflammatory effects of blood‐serum‐derived exosomes in treatment of acute inflammation following TT in mice were evaluated. MATERIALS AND METHODS: Eighteen male mice were grouped as healthy control, TT, and TT + exosome. TT was induced surgically, and exosomes were extracted from blood serum and administrated by a single intratesticular injection (10 IU). Malondialdehyde (MDA) and Griess assays were used to evaluate the level of oxidative stress. Sperm indices, testosterone (Tes), and apoptotic gene expression (p‐53, Bcl2, and Caspase‐3) were also assessed. H&E and immunohistochemistry (IHC) stainings were used for histopathological investigations. Data analysis was applied by SPSS (v.19) software. RESULTS: Oxidative stress and apoptotic genes expression were increased significantly (p < 0.05) in TT group compared with control. Sperm parameters and Tes were significantly increased, and expression of apoptotic genes was significantly reduced in TT + exosome group (p < 0.05). CONCLUSION: Since the blood‐serum‐derived exosomes have anti‐inflammatory features, the intratesticular application of blood‐serum‐derived exosomes can be used clinically in acute phase of orchitis following TT to inhibit testicular inflammation. John Wiley and Sons Inc. 2022-05-20 /pmc/articles/PMC9434569/ /pubmed/35593125 http://dx.doi.org/10.1002/ame2.12232 Text en © 2022 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Keivan, Mona
Mansouri Torghabeh, Fatemeh
Davoodi, Samira
Moradi Maryamneghari, Shima
Dadfar, Reza
Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title_full Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title_fullStr Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title_full_unstemmed Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title_short Single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
title_sort single intratesticular injection of blood‐serum‐derived exosomes can potentially alleviate testopathy following testicular torsion
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434569/
https://www.ncbi.nlm.nih.gov/pubmed/35593125
http://dx.doi.org/10.1002/ame2.12232
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