Oral exposure to methylmercury modifies the prostatic microenvironment in adult rats
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
07/11/2013
07/11/2013
2012
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Resumo |
Methylmercury (MeHg) is an environmental pollutant that is highly toxic to the central nervous system. As its effects on male reproductive system are poorly understood, this study was carried out to analyse the effects of MeHg on the rat prostate. To evaluate the MeHg toxicity on ventral prostate, three groups of adult male Wistar rats received oral doses of 0.5, 1.0 and 3.0mg/kg MeHg, respectively, on a daily basis for 14days. A fourth group was used as a control. The prostate weight was decreased in rats treated orally with 0.5mg/kg MeHg compared to controls. Also, Hg concentration increased significantly in the prostate after treatments. There were reductions in serum testosterone levels and androgen receptor immunoreactivity in animals receiving 3.0mgMeHg/kg. The stereological data showed changes in the prostatic epithelial, stromal and luminal compartments which varied according to the different doses. Histopathological alterations, such as chronic inflammation, stratified epithelial hyperplasia and epithelial inflammatory reactive atypia, were observed in the 0.5mg/kg MeHg-treated group. Epithelial atrophy was observed in the 3.0mg/kg MeHg-treated group. In conclusion, the MeHg affects prostatic homoeostasis resulting in histopathological changes that may be relevant in the pathogenesis of prostatic disease. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2007/56458-4] |
Identificador |
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, HOBOKEN, v. 93, n. 5, p. 354-360, OCT, 2012 0959-9673 http://www.producao.usp.br/handle/BDPI/42801 10.1111/j.1365-2613.2012.00825.x |
Idioma(s) |
eng |
Publicador |
WILEY-BLACKWELL HOBOKEN |
Relação |
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY |
Direitos |
closedAccess Copyright WILEY-BLACKWELL |
Palavras-Chave | #ADULT MALE RAT #ANDROGEN RECEPTOR #INDEX PROLIFERATION #METHYLMERCURY #REPRODUCTIVE TOXICITY #VENTRAL PROSTATE #VENTRAL PROSTATE #GLUTATHIONE-PEROXIDASE #MOLECULAR-MECHANISMS #METHYL MERCURY #CANCER #MICE #CARCINOGENESIS #NEUROTOXICITY #SPERMATOGENESIS #INFLAMMATION #PATHOLOGY |
Tipo |
article original article publishedVersion |