Evidence map›Paper›PMID 42700322›Full record

ArticleBiometals : an international journal on the role of metal ions in biology, biochemistry, and medicine2026

Toxicological evidence that methylmercury exposure amplifies bone destruction and systemic impact associated with apical periodontitis in rats.

Daiane Claydes Baia-da-Silva, Paulo Fernando Santos Mendes, Vinicius Ruan Neves Dos Santos, Deiweson Souza-Monteiro, Rayssa Maitê Farias Nazário, Leonardo Oliveira Bittencourt, Charles Miller de Souza Borges, Kelly das Graças Fernandes Dantas, Douglas Magno Guimarães, Fabricio Mezzomo Collares and 2 more

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Article in Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Daiane Claydes Baia-da-SilvaLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0000-0002-7133-6391
Paulo Fernando Santos MendesLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0000-0001-5495-0835
Vinicius Ruan Neves Dos SantosLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0000-0002-6486-4700
Deiweson Souza-MonteiroLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0000-0003-1843-4184
Rayssa Maitê Farias NazárioLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0009-0005-8119-746X
Leonardo Oliveira BittencourtLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil.ORCID http://orcid.org/0000-0002-9525-2723
Charles Miller de Souza BorgesGroup of Applied Analytical Spectrometry, Institute of Natural and Exact Sciences, Federal University of Pará, Belém, Pará, Brazil.ORCID http://orcid.org/0009-0001-8931-5652
Kelly das Graças Fernandes DantasGroup of Applied Analytical Spectrometry, Institute of Natural and Exact Sciences, Federal University of Pará, Belém, Pará, Brazil.ORCID http://orcid.org/0000-0002-5424-2908
Douglas Magno GuimarãesDepartment of Oral Pathology, University Center of Pará, Belem, Pará, Brazil.ORCID http://orcid.org/0000-0001-7856-1324
Fabricio Mezzomo CollaresDental Material Laboratory, School of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.ORCID http://orcid.org/0000-0002-1382-0150
Rogerio Castilho JacintoDepartment of Restorative Dentistry, Araçatuba School of Dentistry, Endodontics, São Paulo State University (UNESP), São Paulo, Brazil.ORCID http://orcid.org/0000-0002-2362-8920
Rafael Rodrigues LimaLaboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará, Augusto Corrêa Street, Guamá, Belém, Pará, 66075-110, Brazil. rafalima@ufpa.br.ORCID https://orcid.org/0000-0003-1486-4013

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated whether long-term methylmercury exposure aggravates apical periodontitis in Wistar rats. Thirty-two male rats (90 days old) were randomized into four groups (n = 8): control, methylmercury, apical periodontitis, and methylmercury + apical periodontitis. Methylmercury was administered daily by intragastric gavage (0.04 mg/kg/day) for 60 days, while apical periodontitis was induced on day 32 by pulp exposure to the oral cavity for 28 days. After euthanasia, total mercury levels and systemic oxidative stress markers were analyzed in blood; additionally, mandibles were evaluated for lesion volume and alveolar bone quality using micro-computed tomography and histological analysis. Data were analyzed using the Shapiro-Wilk test, followed by two-way ANOVA and Tukey's post hoc test (p < 0.05). The methylmercury + apical periodontitis group showed significantly larger periapical lesions and reduced alveolar bone quality compared to non-exposed animals (p < 0.05), with decreased trabecular thickness, lower bone volume/tissue volume ratio, and increased tissue destruction. Moreover, this group exhibited more intense oxidative alterations, including reduced antioxidant defenses (reduced glutathione and total antioxidant capacity equivalent to Trolox) and increased lipid peroxidation. Therefore, under the conditions of the present experimental model, long-term methylmercury exposure preceding and overlapping with apical periodontitis development resulted in increased lesion volume, impaired alveolar bone quality, and more pronounced systemic oxidative alterations, indicating an aggravation of apical periodontitis.

Indexed as

Alveolar bone lossAnimal modelApical periodontitisMethylmercuryMicro-CTOxidative stress

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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.