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Vitamin B12 prevents cimetidine-induced androgenic failure and damage to sperm quality in rats

dc.contributor.authorBeltrame, Flávia L.
dc.contributor.authorDe Santi, Fabiane
dc.contributor.authorVendramini, Vanessa
dc.contributor.authorCabral, Regina E.
dc.contributor.authorMiraglia, Sandra M.
dc.contributor.authorCerri, Paulo S. [UNESP]
dc.contributor.authorCerri, Estela S. [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2019-10-06T16:49:51Z
dc.date.available2019-10-06T16:49:51Z
dc.date.issued2019-01-01
dc.description.abstractCimetidine, 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 B12 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 B12 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 (100mg/kg of cimetidine), cimetidine/vitamin B12 group (100mg/kg of cimetidine + 3µg vitamin B12), vitamin B12 group (3µg vitamin B12) 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 was 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 B12 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.en
dc.description.affiliationPaulista Medical School Federal University of São Paulo
dc.description.affiliationPaulista School of Nursing Federal University of Sao Paulo
dc.description.affiliationUniversidade Estadual Paulista Júlio de Mesquita Filho (UNESP) Câmpus de Araraquara, Araraquara
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho (UNESP) Câmpus de Araraquara, Araraquara
dc.identifierhttp://dx.doi.org/10.3389/fendo.2019.00309
dc.identifier.citationFrontiers in Endocrinology, v. 10, n. APR, 2019.
dc.identifier.doi10.3389/fendo.2019.00309
dc.identifier.issn1664-2392
dc.identifier.scopus2-s2.0-85067675366
dc.identifier.urihttp://hdl.handle.net/11449/189716
dc.language.isoeng
dc.relation.ispartofFrontiers in Endocrinology
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAndrogenic dysfunction
dc.subjectCimetidine
dc.subjectDNA Damage
dc.subjectSperm quality
dc.subjectSpermiogenesis
dc.subjectVitamin B12
dc.titleVitamin B12 prevents cimetidine-induced androgenic failure and damage to sperm quality in ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationcb428e10-1b21-4b42-b871-01f3ebf27e66
relation.isDepartmentOfPublication.latestForDiscoverycb428e10-1b21-4b42-b871-01f3ebf27e66
relation.isOrgUnitOfPublicationa3cdb24b-db92-40d9-b3af-2eacecf9f2ba
relation.isOrgUnitOfPublication.latestForDiscoverya3cdb24b-db92-40d9-b3af-2eacecf9f2ba
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentEnfermagem - FMBpt

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