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Molecular damage and responses of oral keratinocyte to hydrogen peroxide

BACKGROUND: Hydrogen peroxide (H(2)O(2))-based tooth bleaching reagents have recently increased in popularity and controversy. H(2)O(2) gel (3%) is used in a Nightguard for vital bleaching; transient tooth sensitivity and oral mucosa irritation have been reported. Genotoxicity and carcinogenicity ha...

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Autores principales: Lin, Kuan-Yu, Chung, Ching-Hung, Ciou, Jheng-Sian, Su, Pei-Fang, Wang, Pei-Wen, Shieh, Dar-Bin, Wang, Tzu-Chueh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329095/
https://www.ncbi.nlm.nih.gov/pubmed/30634966
http://dx.doi.org/10.1186/s12903-018-0694-0
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author Lin, Kuan-Yu
Chung, Ching-Hung
Ciou, Jheng-Sian
Su, Pei-Fang
Wang, Pei-Wen
Shieh, Dar-Bin
Wang, Tzu-Chueh
author_facet Lin, Kuan-Yu
Chung, Ching-Hung
Ciou, Jheng-Sian
Su, Pei-Fang
Wang, Pei-Wen
Shieh, Dar-Bin
Wang, Tzu-Chueh
author_sort Lin, Kuan-Yu
collection PubMed
description BACKGROUND: Hydrogen peroxide (H(2)O(2))-based tooth bleaching reagents have recently increased in popularity and controversy. H(2)O(2) gel (3%) is used in a Nightguard for vital bleaching; transient tooth sensitivity and oral mucosa irritation have been reported. Genotoxicity and carcinogenicity have also been significant concerns. METHODS: We used primary cultured normal human oral keratinocytes (NHOKs) as an in vitro model to investigate the pathological effects to mitochondria functions on human oral keratinocytes exposed to different doses of H(2)O(2) for different durations. RESULTS: An MTT assay showed compromised cell viability at a dose over 5 mM. The treatments induced nuclear DNA damage, measured using a single-cell gel electrophoresis assay. A real-time quantitative polymerase chain reaction showed H(2)O(2) induced significant increase in mitochondrial 4977-bp deletion. Mitochondrial membrane potential and apoptosis assays suggested that oxidative damage defense mechanisms were activated after prolonged exposure to H(2)O(2). Reduced intracellular glutathione was an effective defense against oxidative damage from 5 mM of H(2)O(2). CONCLUSION: Our study suggests the importance for keratinocyte damage of the dose and the duration of the exposure to H(2)O(2) in at-home-bleaching. A treatment dose ≥100 mM directly causes severe cytotoxicity with as little as 15 min of exposure.
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spelling pubmed-63290952019-01-16 Molecular damage and responses of oral keratinocyte to hydrogen peroxide Lin, Kuan-Yu Chung, Ching-Hung Ciou, Jheng-Sian Su, Pei-Fang Wang, Pei-Wen Shieh, Dar-Bin Wang, Tzu-Chueh BMC Oral Health Research Article BACKGROUND: Hydrogen peroxide (H(2)O(2))-based tooth bleaching reagents have recently increased in popularity and controversy. H(2)O(2) gel (3%) is used in a Nightguard for vital bleaching; transient tooth sensitivity and oral mucosa irritation have been reported. Genotoxicity and carcinogenicity have also been significant concerns. METHODS: We used primary cultured normal human oral keratinocytes (NHOKs) as an in vitro model to investigate the pathological effects to mitochondria functions on human oral keratinocytes exposed to different doses of H(2)O(2) for different durations. RESULTS: An MTT assay showed compromised cell viability at a dose over 5 mM. The treatments induced nuclear DNA damage, measured using a single-cell gel electrophoresis assay. A real-time quantitative polymerase chain reaction showed H(2)O(2) induced significant increase in mitochondrial 4977-bp deletion. Mitochondrial membrane potential and apoptosis assays suggested that oxidative damage defense mechanisms were activated after prolonged exposure to H(2)O(2). Reduced intracellular glutathione was an effective defense against oxidative damage from 5 mM of H(2)O(2). CONCLUSION: Our study suggests the importance for keratinocyte damage of the dose and the duration of the exposure to H(2)O(2) in at-home-bleaching. A treatment dose ≥100 mM directly causes severe cytotoxicity with as little as 15 min of exposure. BioMed Central 2019-01-11 /pmc/articles/PMC6329095/ /pubmed/30634966 http://dx.doi.org/10.1186/s12903-018-0694-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lin, Kuan-Yu
Chung, Ching-Hung
Ciou, Jheng-Sian
Su, Pei-Fang
Wang, Pei-Wen
Shieh, Dar-Bin
Wang, Tzu-Chueh
Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title_full Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title_fullStr Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title_full_unstemmed Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title_short Molecular damage and responses of oral keratinocyte to hydrogen peroxide
title_sort molecular damage and responses of oral keratinocyte to hydrogen peroxide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329095/
https://www.ncbi.nlm.nih.gov/pubmed/30634966
http://dx.doi.org/10.1186/s12903-018-0694-0
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