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.
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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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.
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