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Parenteral monofluorophosphate (MFP) is a more potent inducer of enamel fluorotic defects in neonatal hamster molars than sodium fluoride

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Abstract

Supra-optimal intake of sodium fluoride (NaF) during early childhood results in formation of irreversible enamel defects. Monofluorophosphate (MFP) was considered as less toxic than NaF but equally cariostatic. We compared the potency of MFP and NaF to induce pre-eruptive sub-ameloblastic cysts and post-eruptive white spots and pits in developing hamster enamel. Hamster pups were injected subcutaneously with either NaF or MFP in equimolar doses of either 9 mg or 18 mg F/kg body weight. At 9 mg F/kg, MFP induced more but smaller sub-ameloblastic cysts with a collective cyst volume twice as large as that induced by NaF. Eight days after F injection, all F-injected groups had formed 4–6 white spots per molar, with an additional 2 pits per molar in the low MFP group. Twenty-eight days after injection, most white spots had turned into pits (5–6 per molar) and only the high MFP group still contained 2 white spots per molar. We conclude that parenterally applied MFP is more potent in inducing enamel defects than NaF. Most white spots formed turn into pits by functional use of the dentition. The higher potency of parenteral MFP may be associated with sustained elevated F levels in the enamel organ by enzymatic hydrolysis of MFP by alkaline phosphatase activity.

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References

  1. Fejerskov O, Larsen MJ, Richards A, Baelum V. Dental tissue effects of fluoride. Adv Dent Res. 1994;8:15–31.

    PubMed  Google Scholar 

  2. Robinson C, Connell S, Kirkham J, Brookes SJ, Shore RC. The effect of fluoride on the developing tooth. Caries Res. 2004;38:268–76.

    PubMed  Google Scholar 

  3. Aoba T, Fejerskov O. Dental fluorosis: chemistry and biology. Crit Rev Oral Biol Med. 2002;13:155–70.

    PubMed  Google Scholar 

  4. DenBesten P, Li W. Chronic fluoride toxicity: dental fluorosis. Monogr Oral Sci. 2011;22:81–96.

    PubMed Central  PubMed  Google Scholar 

  5. Stephen KW. The value of anti-caries and antiplaque dentrifices at a community level. Ad Dent Res. 1995;9:127–8.

    Google Scholar 

  6. Whitford GM. The physiological and toxicological characteristics of fluoride. J Dent Res. 1990; 69 special issue 539–49.

    Google Scholar 

  7. Shourie KL, Hein JW, Hodge HC. Preliminary studies of the caries inhibiting potential and acute toxicity of sodium monofluorophosphate. J Dent Res. 1950;29:529–33.

    PubMed  Google Scholar 

  8. Lim K, Renaldo GJ, Chapman P. LD50 of SnF2, NaF and Na2PO3F in the mouse compared to the rat. Caries Res. 1978;12:177–9.

    PubMed  Google Scholar 

  9. Baylink DJ, Duane PB, Farley SM, Farley JR. Monofluorophosphate physiology: the effects of fluoride on bone. Caries Res. 1983;17(Suppl 1):56–76.

    PubMed  Google Scholar 

  10. Ericsson Y, Santesson G, Ullberg S. Absorption and metabolism of PO3F ion in the animal body. Studies with F18, P32 labelled monofluorophosphate. Arch Oral Biol. 1961;4:160–74.

    Google Scholar 

  11. Ericsson Y. Biologic splitting of PO3F-ions. Caries Res. 1967;1:144–52.

    PubMed  Google Scholar 

  12. Ericsson Y, Patterson C. Studies on the hydrolysis and absorption of monofluorophosphate ions. Pharmacol Ther Dent. 1980;5:47–54.

    PubMed  Google Scholar 

  13. Setnikar S, Arigoni R. Chemical stability and mode of gastrointestinal absorption of sodium monofluorophosphate. Arzneimittelforschung. 1988;38:45–9.

    PubMed  Google Scholar 

  14. Pearce EI, Jenkins GN. The decomposition of monofluorophosphate by enzymes in whole human saliva. Arch Oral Biol. 1977;22:405–7.

    PubMed  Google Scholar 

  15. Farley JR, Trabeaux NM, Lau KHW, Baylink DJ. Monofluorophosphate is hydrolysed by alkaline phosphatase and mimics the actions of NaF on skeletal tissues in vitro. Calcif Tissue Int. 1987;40:35–42.

    PubMed  Google Scholar 

  16. Pearce EI, Dibdin GH. The effect of pH, temperature and plaque thickness on the hydrolysis of monofluorophosphate in experimental dental plaque. Caries Res. 2003;37:178–84.

    PubMed  Google Scholar 

  17. Poulsen H, Ericsson Y. Chronic toxicity of dietary sodium monofluorophosphate in growing rats with special reference to kidney changes. Acta Pathol Microbiol Scand. 1965;65:493–504.

    PubMed  Google Scholar 

  18. Hein JW, Marcusson HW, Quigley G. Comparative effect of Na2FPO3 and NaF on erupting incisors. IADR 35th Gen Meeting abstract 1957.

  19. Lyaruu DM, Alberga JM, Kwee NC, Bervoets TJ, Bronckers AL, DenBesten PK. Fate of fluoride-induced sub-ameloblastic cysts in developing hamster molar tooth germs. Arch Oral Biol. 2011;56:238–43.

    PubMed  Google Scholar 

  20. Lyaruu DM, Vermeulen L, Stienen N, Bervoets TJ, DenBesten PK, Bronckers AL. Enamel pits in hamster molars, formed by a single high fluoride dose, are associated with a perturbation of transitional stage ameloblasts. Caries Res. 2012;46:575–80.

    PubMed Central  PubMed  Google Scholar 

  21. Trautner K, Einwag J. Human plasma fluoride levels following intake of dentifrices containing aminefluoride or monofluorophosphate. Arch Oral Biol. 1988;33:543–6.

    PubMed  Google Scholar 

  22. Erlacher L, Teufelsbauer H, Bernicker P, Pietschmann P, Weissel M. Comparison of serum fluoride levels after administration of monofluorophosphate-calcium carbonate or sodium fluoride; differences in peak serum concentrations. Clin Invest. 1994;72:1082–5.

    Google Scholar 

  23. Whitford GM, Pashley DH, Allison NB. Effects of fluoride on bone. Discussion. Caries Res 1983; 17 (suppl 1):69–76.

    Google Scholar 

  24. Esteban L, Rigalli A, Puche RC. Metabolism of the complex monofluorophosphate-alpha 2—macroglobulin in the rat. Medicina (B aires). 1999;59:151–6.

    Google Scholar 

  25. Bijella MF, Brighenti FL, Bijella MF, Buzalaf MA. Fluoride kinetics in saliva after the use of a fluoride-containing chewing gum. Braz Oral Res. 2005;19:256–60.

    PubMed  Google Scholar 

  26. Nuki K, Bonting SL. Quantitative histochemistry of the developing hamster tooth: alkaline phosphatase and lactic dehydrogenase. J Histochem Cytochem. 1961;9:117–25.

    PubMed  Google Scholar 

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Acknowledgments

The work has been supported in part by NIH grant DE13508.

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Correspondence to Antonius L. J. J. Bronckers.

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Lyaruu, D.M., Schoonderwoerd, M., Tio, D. et al. Parenteral monofluorophosphate (MFP) is a more potent inducer of enamel fluorotic defects in neonatal hamster molars than sodium fluoride. Odontology 102, 147–153 (2014). https://doi.org/10.1007/s10266-013-0119-0

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