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Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats
Cimetidine, used as an anti-ulcer and adjuvant treatment in cancer therapy, causes disorders in the male reproductive tract, including steroidogenesis. However, its effect on sperm quality and male fertility has been poorly addressed. Since vitamin B(12) has demonstrated to recover spermatogonia num...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635670/ https://www.ncbi.nlm.nih.gov/pubmed/31354617 http://dx.doi.org/10.3389/fendo.2019.00309 |
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author | Beltrame, Flávia Luciana de Santi, Fabiane Vendramini, Vanessa Cabral, Regina Elizabeth Lourenço Miraglia, Sandra Maria Cerri, Paulo Sérgio Sasso-Cerri, Estela |
author_facet | Beltrame, Flávia Luciana de Santi, Fabiane Vendramini, Vanessa Cabral, Regina Elizabeth Lourenço Miraglia, Sandra Maria Cerri, Paulo Sérgio Sasso-Cerri, Estela |
author_sort | Beltrame, Flávia Luciana |
collection | PubMed |
description | Cimetidine, used as an anti-ulcer and adjuvant treatment in cancer therapy, causes disorders in the male reproductive tract, including steroidogenesis. However, its effect on sperm quality and male fertility has been poorly addressed. Since vitamin B(12) has demonstrated to recover spermatogonia number and sperm concentration in cimetidine-treated rats, we evaluated the impact of cimetidine on sperm quality and fertility potential and whether vitamin B(12) is able to prevent the harmful effect of this drug on steroidogenesis and sperm parameters. Adult male rats were treated for 52 consecutive days as follows: cimetidine group (100 mg/kg of cimetidine), cimetidine/vitamin B(12) group (100 mg/kg of cimetidine + 3 μg vitamin B(12)), vitamin B(12) group (3 μg vitamin B(12)) and control group (saline). Serum testosterone levels and immunofluorescence associated to western blot for detection of 17β-HSD6 were performed. Sperm morphology and motility, mitochondrial activity, acrosome integrity, DNA integrity by Comet assay, lipid peroxidation as well as fertility potential were analyzed in all groups. Apoptotic spermatids were also evaluated by caspase-3 immunohistochemistry. In the cimetidine-treated animals, reduced serum testosterone levels, weak 17β-HSD6 levels and impaired spermiogenesis were observed. Low sperm motility and mitochondrial activity were associated with high percentage of sperm tail abnormalities, and the percentage of spermatozoa with damaged acrosome and DNA fragmentation increased. MDA levels were normal in all groups, indicating that the cimetidine-induced changes are associated to androgenic failure. In conclusion, despite the fertility potential of rats was unaffected by the treatment, the sperm quality was significantly impaired. Therefore, considering a possible sperm-mediated transgenerational inheritance, the long term offspring health needs to be investigated. The administration of vitamin B(12) to male rats prevents the androgenic failure and counteracts the damage inflicted by cimetidine upon sperm quality, indicating that this vitamin may be used as a therapeutic agent to maintain the androgenic status and the sperm quality in patients exposed to androgen disrupters. |
format | Online Article Text |
id | pubmed-6635670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66356702019-07-26 Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats Beltrame, Flávia Luciana de Santi, Fabiane Vendramini, Vanessa Cabral, Regina Elizabeth Lourenço Miraglia, Sandra Maria Cerri, Paulo Sérgio Sasso-Cerri, Estela Front Endocrinol (Lausanne) Endocrinology Cimetidine, used as an anti-ulcer and adjuvant treatment in cancer therapy, causes disorders in the male reproductive tract, including steroidogenesis. However, its effect on sperm quality and male fertility has been poorly addressed. Since vitamin B(12) has demonstrated to recover spermatogonia number and sperm concentration in cimetidine-treated rats, we evaluated the impact of cimetidine on sperm quality and fertility potential and whether vitamin B(12) is able to prevent the harmful effect of this drug on steroidogenesis and sperm parameters. Adult male rats were treated for 52 consecutive days as follows: cimetidine group (100 mg/kg of cimetidine), cimetidine/vitamin B(12) group (100 mg/kg of cimetidine + 3 μg vitamin B(12)), vitamin B(12) group (3 μg vitamin B(12)) and control group (saline). Serum testosterone levels and immunofluorescence associated to western blot for detection of 17β-HSD6 were performed. Sperm morphology and motility, mitochondrial activity, acrosome integrity, DNA integrity by Comet assay, lipid peroxidation as well as fertility potential were analyzed in all groups. Apoptotic spermatids were also evaluated by caspase-3 immunohistochemistry. In the cimetidine-treated animals, reduced serum testosterone levels, weak 17β-HSD6 levels and impaired spermiogenesis were observed. Low sperm motility and mitochondrial activity were associated with high percentage of sperm tail abnormalities, and the percentage of spermatozoa with damaged acrosome and DNA fragmentation increased. MDA levels were normal in all groups, indicating that the cimetidine-induced changes are associated to androgenic failure. In conclusion, despite the fertility potential of rats was unaffected by the treatment, the sperm quality was significantly impaired. Therefore, considering a possible sperm-mediated transgenerational inheritance, the long term offspring health needs to be investigated. The administration of vitamin B(12) to male rats prevents the androgenic failure and counteracts the damage inflicted by cimetidine upon sperm quality, indicating that this vitamin may be used as a therapeutic agent to maintain the androgenic status and the sperm quality in patients exposed to androgen disrupters. Frontiers Media S.A. 2019-07-10 /pmc/articles/PMC6635670/ /pubmed/31354617 http://dx.doi.org/10.3389/fendo.2019.00309 Text en Copyright © 2019 Beltrame, de Santi, Vendramini, Cabral, Miraglia, Cerri and Sasso-Cerri. http://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 | Endocrinology Beltrame, Flávia Luciana de Santi, Fabiane Vendramini, Vanessa Cabral, Regina Elizabeth Lourenço Miraglia, Sandra Maria Cerri, Paulo Sérgio Sasso-Cerri, Estela Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title | Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title_full | Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title_fullStr | Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title_full_unstemmed | Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title_short | Vitamin B(12) Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats |
title_sort | vitamin b(12) prevents cimetidine-induced androgenic failure and damage to sperm quality in rats |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635670/ https://www.ncbi.nlm.nih.gov/pubmed/31354617 http://dx.doi.org/10.3389/fendo.2019.00309 |
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