60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.

Mercury is a toxic and bio-accumulative heavy metal of global concern. While good deals of research have been conducted on the toxic effects of mercury, little is known about the mechanisms involved in the pathogenesis of male reproductive dysfunction induced by mercury. Therefore, the purpose of th...

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Autores principales: Caroline S Martinez, João Guilherme D Torres, Franck M Peçanha, Janete A Anselmo-Franci, Dalton V Vassallo, Mercedes Salaices, María J Alonso, Giulia A Wiggers
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/45b5cea0a9534fb7b89c3007d6459a21
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spelling oai:doaj.org-article:45b5cea0a9534fb7b89c3007d6459a212021-11-25T05:54:45Z60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.1932-620310.1371/journal.pone.0111202https://doaj.org/article/45b5cea0a9534fb7b89c3007d6459a212014-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0111202https://doaj.org/toc/1932-6203Mercury is a toxic and bio-accumulative heavy metal of global concern. While good deals of research have been conducted on the toxic effects of mercury, little is known about the mechanisms involved in the pathogenesis of male reproductive dysfunction induced by mercury. Therefore, the purpose of this study was to assess the effects and underlying mechanisms of chronic mercury exposure at low levels on male reproductive system of rats. Three-month-old male Wistar rats were divided into two groups and treated for 60 days with saline (i.m., Control) and HgCl2 (i.m. 1st dose: 4.6 µg/kg, subsequent doses 0.07 µg/kg/day). We analyzed sperm parameters, hormonal levels and biomarkers of oxidative stress in testis, epididymis, prostate and vas deferens. Mercury treatment decreased daily sperm production, count and motility and increased head and tail morphologic abnormalities. Moreover, mercury treatment decreased luteinizing hormone levels, increased lipid peroxidation on testis and decreased antioxidant enzymes activities (superoxide dismutase and catalase) on reproductive organs. Our data demonstrate that 60-day chronic exposure to low concentrations of HgCl2 impairs sperm quality and promotes hormonal imbalance. The raised oxidative stress seems to be a potential mechanism involved on male reproductive toxicity by mercury.Caroline S MartinezJoão Guilherme D TorresFranck M PeçanhaJanete A Anselmo-FranciDalton V VassalloMercedes SalaicesMaría J AlonsoGiulia A WiggersPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 11, p e111202 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Caroline S Martinez
João Guilherme D Torres
Franck M Peçanha
Janete A Anselmo-Franci
Dalton V Vassallo
Mercedes Salaices
María J Alonso
Giulia A Wiggers
60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
description Mercury is a toxic and bio-accumulative heavy metal of global concern. While good deals of research have been conducted on the toxic effects of mercury, little is known about the mechanisms involved in the pathogenesis of male reproductive dysfunction induced by mercury. Therefore, the purpose of this study was to assess the effects and underlying mechanisms of chronic mercury exposure at low levels on male reproductive system of rats. Three-month-old male Wistar rats were divided into two groups and treated for 60 days with saline (i.m., Control) and HgCl2 (i.m. 1st dose: 4.6 µg/kg, subsequent doses 0.07 µg/kg/day). We analyzed sperm parameters, hormonal levels and biomarkers of oxidative stress in testis, epididymis, prostate and vas deferens. Mercury treatment decreased daily sperm production, count and motility and increased head and tail morphologic abnormalities. Moreover, mercury treatment decreased luteinizing hormone levels, increased lipid peroxidation on testis and decreased antioxidant enzymes activities (superoxide dismutase and catalase) on reproductive organs. Our data demonstrate that 60-day chronic exposure to low concentrations of HgCl2 impairs sperm quality and promotes hormonal imbalance. The raised oxidative stress seems to be a potential mechanism involved on male reproductive toxicity by mercury.
format article
author Caroline S Martinez
João Guilherme D Torres
Franck M Peçanha
Janete A Anselmo-Franci
Dalton V Vassallo
Mercedes Salaices
María J Alonso
Giulia A Wiggers
author_facet Caroline S Martinez
João Guilherme D Torres
Franck M Peçanha
Janete A Anselmo-Franci
Dalton V Vassallo
Mercedes Salaices
María J Alonso
Giulia A Wiggers
author_sort Caroline S Martinez
title 60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
title_short 60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
title_full 60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
title_fullStr 60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
title_full_unstemmed 60-Day chronic exposure to low concentrations of HgCl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
title_sort 60-day chronic exposure to low concentrations of hgcl2 impairs sperm quality: hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/45b5cea0a9534fb7b89c3007d6459a21
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