Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71897
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dc.contributor.authorNutcha Jariyamanaen_US
dc.contributor.authorPatchanee Chuveeraen_US
dc.contributor.authorAnat Dewien_US
dc.contributor.authorWarat Leelapornpisiden_US
dc.contributor.authorJitjiroj Ittichaicharoenen_US
dc.contributor.authorSiriporn Chattipakornen_US
dc.contributor.authorTanida Srisuwanen_US
dc.date.accessioned2021-01-27T04:17:11Z-
dc.date.available2021-01-27T04:17:11Z-
dc.date.issued2021-01-01en_US
dc.identifier.issn14363771en_US
dc.identifier.issn14326981en_US
dc.identifier.other2-s2.0-85099040852en_US
dc.identifier.other10.1007/s00784-020-03721-7en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85099040852&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/71897-
dc.description.abstract© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature. Objectives: N-Acetyl cysteine (NAC), a well-known antioxidant molecule, has been used to modulate oxidative stress and inflammation. However, no studies have examined the effect of NAC in regenerative endodontic procedures (REPs). Therefore, the aim of this study was to investigate the effects of NAC on cell survival, mitochondrial reactive oxygen species (mtROS) production, and inflammatory and mitochondria-related gene expression on lipopolysaccharide (LPS)-treated apical papilla cells (APCs). Materials and methods: To assess the NAC concentration, 5 and 10 mM NAC were administered to LPS-treated APCs. Cell proliferation was measured at 24, 48, and 72 h by using AlamarBlue® assay. The 5-mM concentration was further analyzed using different treatment durations: 10 min, 24 h, and the entire study period. The mtROS production was quantified using MitoSOX™ Red and MitoTracker™ Green. RT-PCR was used to detect the expression of IL-6 and TNF-α inflammatory genes and mitochondrial morphology–related genes (Mfn-2/Drp-1 and Bcl-2/Bax) at 6 and 24 h. The statistical significance level was set at 0.05. Results: Five-millimolar NAC promoted the highest LPS-treated APC proliferation. The use of 24-h NAC stimulated cell proliferation, whereas the entire-period NAC application (> 48 h) significantly reduced the cell number. The mtROS levels were slightly altered after NAC induction. Ten-minute NAC treatment downregulated the IL-6 and TNF-α expression, whereas the expression of Bcl-2/Bax and Mfn-2/Drp-1 ratios was upregulated at 6 h. Conclusions: Under the LPS-induced inflammatory condition, NAC stimulated APC survival and decreased inflammation. Ten-minute NAC treatment was sufficient to reduce the level of inflammation and maintain the mitochondrial dynamics. Clinical relevance: Ten-minute NAC application is sufficient to reduce the level of inflammation and maintain the mitochondrial dynamics. Therefore, NAC may be considered as a potential adjunctive irrigation solution in REPs.en_US
dc.subjectDentistryen_US
dc.titleEffects of N-acetyl cysteine on mitochondrial ROS, mitochondrial dynamics, and inflammation on lipopolysaccharide-treated human apical papilla cellsen_US
dc.typeJournalen_US
article.title.sourcetitleClinical Oral Investigationsen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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