Abstract

ObjectiveThis study aimed to assess the overall apatite crystals profile in the enamel matrix of mice susceptible (A/J strain) or resistant (129P3/J strain) to dental fluorosis through analyses by atomic force microscopy (AFM).Material and MethodsSamples from the enamel matrix in the early stages of secretion and maturation were obtained from the incisors of mice from both strains. All detectable traces of matrix protein were removed from the samples by a sequential extraction procedure. The purified crystals (n=13 per strain) were analyzed qualitatively in the AFM. Surface roughness profile (Ra) was measured.ResultsThe mean (±SD) Ra of the crystals of A/J strain (0.58±0.15 nm) was lower than the one found for the 129P3/J strain (0.66±0.21 nm) but the difference did not reach statistical significance (t=1.187, p=0.247). Crystals of the 129P3/J strain (70.42±6.79 nm) were found to be significantly narrower (t=4.013, p=0.0013) than the same parameter measured for the A/J strain (90.42±15.86 nm).ConclusionEnamel crystals of the 129P3/J strain are narrower, which is indicative of slower crystal growth and could interfere in the occurrence of dental fluorosis.

Highlights

  • The widespread use of fluoride (F) has contributed to a reduction in the prevalence and incidence of dental caries worldwide2

  • This led us to the assumption that differences in the profile of the crystals surfaces, regardless exposure to F, would exist between A/J and 129P3/J mice strains and this could have an implication on the mechanisms of dental fluorosis development

  • It was primarily hypothesized that A/J mice would have rougher and wider crystals when compared with 129P3/J mice, which would lead to higher retention of matrix proteins and this could help to explain their increased susceptibility to dental fluorosis

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Summary

Objective

This study aimed to assess the overall apatite crystals profile in the enamel matrix of mice susceptible (A/J strain) or resistant (129P3/J strain) to dental fluorosis through analyses by atomic force microscopy (AFM). Material and Methods: Samples from the enamel matrix in the early stages of secretion and maturation were obtained from the incisors of mice from both strains. The purified crystals (n=13 per strain) were analyzed qualitatively in the AFM. Crystals of the 129P3/J strain (70.42±6.79 nm) were found to be significantly narrower (t=4.013, p=0.0013) than the same parameter measured for the A/J strain (90.42±15.86 nm). Conclusion: Enamel crystals of the 129P3/J strain are narrower, which is indicative of slower crystal growth and could interfere in the occurrence of dental fluorosis

Introduction
Material and Methods
Results
Discussion
Conclusion

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