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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Vitamin B-12 Prevents Cimetidine-Induced Androgenic Failure and Damage to Sperm Quality in Rats

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Author(s):
Beltrame, Flavia Luciana [1] ; de Santi, Fabiane [1] ; Vendramini, Vanessa [1] ; Lourenco Cabral, Regina Elizabeth [1] ; Miraglia, Sandra Maria [1] ; Cerri, Paulo Sergio [2] ; Sasso-Cerri, Estela [2]
Total Authors: 7
Affiliation:
[1] Fed Univ Sao Paulo UNIFESP EPM, Dept Morphol & Genet, Sao Paulo - Brazil
[2] Sao Paulo State Univ UNESP FOAr, Dent Sch, Dept Morphol, Lab Histol & Embryol, Araraquara - Brazil
Total Affiliations: 2
Document type: Journal article
Source: FRONTIERS IN ENDOCRINOLOGY; v. 10, JUL 10 2019.
Web of Science Citations: 0
Abstract

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 mu g vitamin B-12), vitamin B-12 group (3 mu g vitamin B-12) and control group (saline). Serum testosterone levels and immunofluorescence associated to western blot for detection of 17 beta-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 17 beta-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. (AU)

FAPESP's process: 12/23845-3 - Evaluation of Vitamin B12 effect on the mitotic and meiotic phases of spermatogenesis and in the sperm DNA of cimetidine-treated rats
Grantee:Estela Sasso Cerri
Support Opportunities: Regular Research Grants
FAPESP's process: 13/25322-0 - Effect of cimetidine on the epididymal histoarchitecture and evaluation of sperm DNA of rats treated with cimetidine and supplemented with B12
Grantee:Flávia Luciana Beltrame
Support Opportunities: Scholarships in Brazil - Post-Doctoral