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Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms

Arginine is an important pH-elevating agent in the oral cavity. It has been incorporated in oral hygiene formulations to mitigate sensitivity and to prevent caries. In this investigation, the effects of sustained arginine dosing of dental plaque microcosms on bacteriological composition and pH were...

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Autores principales: Ledder, Ruth G., Mistry, Hitesh, Sreenivasan, Prem K., Humphreys, Gavin, McBain, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566835/
https://www.ncbi.nlm.nih.gov/pubmed/28861520
http://dx.doi.org/10.1128/mSphere.00295-17
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author Ledder, Ruth G.
Mistry, Hitesh
Sreenivasan, Prem K.
Humphreys, Gavin
McBain, Andrew J.
author_facet Ledder, Ruth G.
Mistry, Hitesh
Sreenivasan, Prem K.
Humphreys, Gavin
McBain, Andrew J.
author_sort Ledder, Ruth G.
collection PubMed
description Arginine is an important pH-elevating agent in the oral cavity. It has been incorporated in oral hygiene formulations to mitigate sensitivity and to prevent caries. In this investigation, the effects of sustained arginine dosing of dental plaque microcosms on bacteriological composition and pH were evaluated under controlled conditions. Plaque microcosms were established in constant-depth film fermentors (CDFFs) using salivary inocula and fed continuously with artificial saliva. To simulate resting and cariogenic states, the CDFFs were supplemented with sterile water or 5% sucrose, respectively. Plaques were then dosed twice daily with a dentifrice with 1.5% arginine arginine added (DA) or without arginine (DN). This regimen continued for over 3 weeks, after which fermentors were maintained without dosing. Microcosms were analyzed by differential viable counting, with a pH microelectrode, and by eubacterial DNA profiling. Sucrose dosing was associated with significantly (P < 0.001) decreased pH, significantly (P < 0.05) increased counts of total aerobes, Gram-negative anaerobes, aciduric species, acidogenic species, arginine utilizing species, bifidobacteria, lactobacilli and streptococci, and significant (P < 0.05) changes in DNA profiles. Plaques dosed with DA had a significantly (P < 0.001) higher pH than those dosed with DN, with or without sucrose supplementation. Dosing with DA but not DN significantly (P < 0.05) decreased counts of all functional bacterial groups apart from the total anaerobes in cariogenic plaques, and in resting plaques, dosing with DA significantly (P < 0.05) decreased counts of streptococci, lactobacilli, bifidobacteria, and acidogenic bacteria. In summary, sustained exposure of oral microcosms to arginine in formulation significantly increased plaque pH and significantly reduced the viability of cariogenic bacterial species. IMPORTANCE Arginine is used in dental health formulations to help prevent dental cavities. This study assessed the effects of the long-term dosing of laboratory dental plaques with an arginine dentifrice. Data indicate that the addition of arginine dentifrice during sucrose challenge significantly increased plaque pH, thus potentially mitigating cariogenesis. Counts of several functional groups of bacteria associated with tooth decay were significantly decreased in the laboratory plaques during exposure to the arginine dentifrice.
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spelling pubmed-55668352017-08-31 Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms Ledder, Ruth G. Mistry, Hitesh Sreenivasan, Prem K. Humphreys, Gavin McBain, Andrew J. mSphere Research Article Arginine is an important pH-elevating agent in the oral cavity. It has been incorporated in oral hygiene formulations to mitigate sensitivity and to prevent caries. In this investigation, the effects of sustained arginine dosing of dental plaque microcosms on bacteriological composition and pH were evaluated under controlled conditions. Plaque microcosms were established in constant-depth film fermentors (CDFFs) using salivary inocula and fed continuously with artificial saliva. To simulate resting and cariogenic states, the CDFFs were supplemented with sterile water or 5% sucrose, respectively. Plaques were then dosed twice daily with a dentifrice with 1.5% arginine arginine added (DA) or without arginine (DN). This regimen continued for over 3 weeks, after which fermentors were maintained without dosing. Microcosms were analyzed by differential viable counting, with a pH microelectrode, and by eubacterial DNA profiling. Sucrose dosing was associated with significantly (P < 0.001) decreased pH, significantly (P < 0.05) increased counts of total aerobes, Gram-negative anaerobes, aciduric species, acidogenic species, arginine utilizing species, bifidobacteria, lactobacilli and streptococci, and significant (P < 0.05) changes in DNA profiles. Plaques dosed with DA had a significantly (P < 0.001) higher pH than those dosed with DN, with or without sucrose supplementation. Dosing with DA but not DN significantly (P < 0.05) decreased counts of all functional bacterial groups apart from the total anaerobes in cariogenic plaques, and in resting plaques, dosing with DA significantly (P < 0.05) decreased counts of streptococci, lactobacilli, bifidobacteria, and acidogenic bacteria. In summary, sustained exposure of oral microcosms to arginine in formulation significantly increased plaque pH and significantly reduced the viability of cariogenic bacterial species. IMPORTANCE Arginine is used in dental health formulations to help prevent dental cavities. This study assessed the effects of the long-term dosing of laboratory dental plaques with an arginine dentifrice. Data indicate that the addition of arginine dentifrice during sucrose challenge significantly increased plaque pH, thus potentially mitigating cariogenesis. Counts of several functional groups of bacteria associated with tooth decay were significantly decreased in the laboratory plaques during exposure to the arginine dentifrice. American Society for Microbiology 2017-08-23 /pmc/articles/PMC5566835/ /pubmed/28861520 http://dx.doi.org/10.1128/mSphere.00295-17 Text en Copyright © 2017 Ledder et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Ledder, Ruth G.
Mistry, Hitesh
Sreenivasan, Prem K.
Humphreys, Gavin
McBain, Andrew J.
Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title_full Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title_fullStr Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title_full_unstemmed Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title_short Arginine Exposure Decreases Acidogenesis in Long-Term Oral Biofilm Microcosms
title_sort arginine exposure decreases acidogenesis in long-term oral biofilm microcosms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566835/
https://www.ncbi.nlm.nih.gov/pubmed/28861520
http://dx.doi.org/10.1128/mSphere.00295-17
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