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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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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. |
format | Online Article Text |
id | pubmed-10073512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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