Evidence map›Paper›PMID 25368988›Full record

ArticlePloS one2014

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.

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

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Chronic stress reduces spermatogenic cell proliferation in rat testis.International journal of clinical and experimental pathology · 2019
    Article
  8. Review
  9. Frontiers in microbiology · 2018
    Article
  10. Article
  11. Article
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 2 countries.

Caroline S MartinezPostgraduate Program in Biochemistry, Universidade Federal do Pampa, Uruguaiana, Rio Grande do Sul, Brazil.
João Guilherme D TorresPostgraduate Program in Biochemistry, Universidade Federal do Pampa, Uruguaiana, Rio Grande do Sul, Brazil.
Franck M PeçanhaPostgraduate Program in Biochemistry, Universidade Federal do Pampa, Uruguaiana, Rio Grande do Sul, Brazil.
Janete A Anselmo-FranciDepartment of Morphology, Stomatology and Physiology, School of Dentistry, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brazil.
Dalton V VassalloDepartment of Physiological Sciences, Universidade Federal do Espírito Santo, Vitória, Espírito Santo, Brazil.
Mercedes SalaicesDepartment of Pharmacology, School of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
María J AlonsoDepartment of Biochemistry, Physiology and Molecular Genetics, Universidad Rey Juan Carlos, Alcorcón, Spain.
Giulia A WiggersPostgraduate Program in Biochemistry, Universidade Federal do Pampa, Uruguaiana, Rio Grande do Sul, Brazil.
Universidade Federal do Pampa · BRUniversidad Autónoma de Madrid · ESUniversidade de São Paulo · BRUniversidade Federal do Espírito Santo · BRUniversidad Rey Juan Carlos · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AnimalsBody WeightCatalaseImmunoassayLipid PeroxidationLuteinizing HormoneMaleMercuric ChlorideOxidative StressRatsRats, WistarSpermatozoaSperm CountSperm MotilitySuperoxide DismutaseTestosteroneCatalaseLuteinizing HormoneMercuric ChlorideSuperoxide DismutaseTestosterone

Identifiers

PMID25368988
PMCPMC4219708
OpenAlexW2047685370

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.