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Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility

Cancer is a deadly disease characterized by abnormal cell proliferation. Chemotherapy is one technique of cancer treatment. Cyclophosphamide (CYP) is the most powerful chemotherapy medication, yet it has serious adverse effects. It is an antimitotic medicine that regulates cell proliferation and pri...

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Autores principales: Ibrahim, Dalia, Abozied, Nadia, Abdel Maboud, Samar, Alzamami, Ahmad, Alturki, Norah A., Jaremko, Mariusz, Alanazi, Maram Khalil, Alhuthali, Hayaa M., Seddek, Asmaa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073512/
https://www.ncbi.nlm.nih.gov/pubmed/37033609
http://dx.doi.org/10.3389/fphar.2023.1122175
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author Ibrahim, Dalia
Abozied, Nadia
Abdel Maboud, Samar
Alzamami, Ahmad
Alturki, Norah A.
Jaremko, Mariusz
Alanazi, Maram Khalil
Alhuthali, Hayaa M.
Seddek, Asmaa
author_facet Ibrahim, Dalia
Abozied, Nadia
Abdel Maboud, Samar
Alzamami, Ahmad
Alturki, Norah A.
Jaremko, Mariusz
Alanazi, Maram Khalil
Alhuthali, Hayaa M.
Seddek, Asmaa
author_sort Ibrahim, Dalia
collection PubMed
description Cancer is a deadly disease characterized by abnormal cell proliferation. Chemotherapy is one technique of cancer treatment. Cyclophosphamide (CYP) is the most powerful chemotherapy medication, yet it has serious adverse effects. It is an antimitotic medicine that regulates cell proliferation and primarily targets quickly dividing cells, and it has been related to varying levels of infertility in humans. In the current study, we assessed the biochemical, histological, and microscopic evaluations of testicular damage following cyclophosphamide administration. Further, we have explored the potential protective impact of mesenchymal stem cell (MSCs) transplantation. The biochemical results revealed that administration of cyclophosphamide increased serum concentrations of follicle-stimulating hormone (FSH) and luteinizing hormone (LH), while it decreased serum concentrations of free testosterone hormone (TH), testicular follicle-stimulating hormone, luteinizing hormone, and free testosterone hormone concentrations, testicular total antioxidant capacity (TAC), and testicular activity of superoxide dismutase (SOD) enzyme. The histology and sperm examinations revealed that cyclophosphamide induced destruction to the architectures of several tissues in the testes, which drastically reduced the Johnsen score as well as the spermatogenesis process. Surprisingly, transplantation of mesenchymal stem cell after cyclophosphamide administration altered the deterioration effect of cyclophosphamide injury on the testicular tissues, as demonstrated by biochemical and histological analysis. Our results indicated alleviation of serum and testicular sex hormones, as well as testicular oxidative stress markers (total antioxidant capacity and superoxide dismutase activity), and nearly restored the normal appearance of the testicular tissues, Johnsen score, and spermatogenesis process. In conclusion, our work emphasizes the protective pharmacological use of mesenchymal stem cell to mitigate the effects of cyclophosphamide on testicular tissues that impair the spermatogenesis process following chemotherapy. These findings indicate that transferring mesenchymal stem cell to chemotherapy patients could significantly improve spermatogenesis.
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spelling pubmed-100735122023-04-06 Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility Ibrahim, Dalia Abozied, Nadia Abdel Maboud, Samar Alzamami, Ahmad Alturki, Norah A. Jaremko, Mariusz Alanazi, Maram Khalil Alhuthali, Hayaa M. Seddek, Asmaa Front Pharmacol Pharmacology Cancer is a deadly disease characterized by abnormal cell proliferation. Chemotherapy is one technique of cancer treatment. Cyclophosphamide (CYP) is the most powerful chemotherapy medication, yet it has serious adverse effects. It is an antimitotic medicine that regulates cell proliferation and primarily targets quickly dividing cells, and it has been related to varying levels of infertility in humans. In the current study, we assessed the biochemical, histological, and microscopic evaluations of testicular damage following cyclophosphamide administration. Further, we have explored the potential protective impact of mesenchymal stem cell (MSCs) transplantation. The biochemical results revealed that administration of cyclophosphamide increased serum concentrations of follicle-stimulating hormone (FSH) and luteinizing hormone (LH), while it decreased serum concentrations of free testosterone hormone (TH), testicular follicle-stimulating hormone, luteinizing hormone, and free testosterone hormone concentrations, testicular total antioxidant capacity (TAC), and testicular activity of superoxide dismutase (SOD) enzyme. The histology and sperm examinations revealed that cyclophosphamide induced destruction to the architectures of several tissues in the testes, which drastically reduced the Johnsen score as well as the spermatogenesis process. Surprisingly, transplantation of mesenchymal stem cell after cyclophosphamide administration altered the deterioration effect of cyclophosphamide injury on the testicular tissues, as demonstrated by biochemical and histological analysis. Our results indicated alleviation of serum and testicular sex hormones, as well as testicular oxidative stress markers (total antioxidant capacity and superoxide dismutase activity), and nearly restored the normal appearance of the testicular tissues, Johnsen score, and spermatogenesis process. In conclusion, our work emphasizes the protective pharmacological use of mesenchymal stem cell to mitigate the effects of cyclophosphamide on testicular tissues that impair the spermatogenesis process following chemotherapy. These findings indicate that transferring mesenchymal stem cell to chemotherapy patients could significantly improve spermatogenesis. Frontiers Media S.A. 2023-03-22 /pmc/articles/PMC10073512/ /pubmed/37033609 http://dx.doi.org/10.3389/fphar.2023.1122175 Text en Copyright © 2023 Ibrahim, Abozied, Abdel Maboud, Alzamami, Alturki, Jaremko, Alanazi, Alhuthali and Seddek. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Ibrahim, Dalia
Abozied, Nadia
Abdel Maboud, Samar
Alzamami, Ahmad
Alturki, Norah A.
Jaremko, Mariusz
Alanazi, Maram Khalil
Alhuthali, Hayaa M.
Seddek, Asmaa
Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title_full Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title_fullStr Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title_full_unstemmed Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title_short Therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
title_sort therapeutic potential of bone marrow mesenchymal stem cells in cyclophosphamide-induced infertility
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073512/
https://www.ncbi.nlm.nih.gov/pubmed/37033609
http://dx.doi.org/10.3389/fphar.2023.1122175
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