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Two mechanisms of oral malodor inhibition by zinc ions

OBJECTIVES: The aim of this study was to reveal the mechanisms by which zinc ions inhibit oral malodor. MATERIAL AND METHODS: The direct binding of zinc ions to gaseous hydrogen sulfide (H(2)S) was assessed in comparison with other metal ions. Nine metal chlorides and six metal acetates were examine...

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Detalles Bibliográficos
Autores principales: Suzuki, Nao, Nakano, Yoshio, Watanabe, Takeshi, Yoneda, Masahiro, Hirofuji, Takao, Hanioka, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade De Odontologia De Bauru - USP 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5777415/
https://www.ncbi.nlm.nih.gov/pubmed/29364345
http://dx.doi.org/10.1590/1678-7757-2017-0161
Descripción
Sumario:OBJECTIVES: The aim of this study was to reveal the mechanisms by which zinc ions inhibit oral malodor. MATERIAL AND METHODS: The direct binding of zinc ions to gaseous hydrogen sulfide (H(2)S) was assessed in comparison with other metal ions. Nine metal chlorides and six metal acetates were examined. To understand the strength of H(2)S volatilization inhibition, the minimum concentration needed to inhibit H(2)S volatilization was determined using serial dilution methods. Subsequently, the inhibitory activities of zinc ions on the growth of six oral bacterial strains related to volatile sulfur compound (VSC) production and three strains not related to VSC production were evaluated. RESULTS: Aqueous solutions of ZnCl(2), CdCl(2), CuCl(2), (CH(3)COO)(2)Zn, (CH(3)COO)(2)Cd, (CH(3)COO)(2)Cu, and CH(3)COOAg inhibited H(2)S volatilization almost entirely. The strengths of H(2)S volatilization inhibition were in the order Ag+ > Cd(2)+ > Cu(2)+ > Zn(2)+. The effect of zinc ions on the growth of oral bacteria was strain-dependent. Fusobacterium nucleatum ATCC 25586 was the most sensitive, as it was suppressed by medium containing 0.001% zinc ions. CONCLUSIONS: Zinc ions have an inhibitory effect on oral malodor involving the two mechanisms of direct binding with gaseous H(2)S and suppressing the growth of VSC-producing oral bacteria.