Cytotoxicity and anti-inflammatory effects of zinc ions and eugenol during setting of ZOE in immortalized human oral keratinocytes grown as three-dimensional spheroids

Jung Hwan Lee, Hae Hyoung Lee, Kyoung Nam Kim, Kwang Mahn Kim

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Objectives The objective of this study is to assess the cytotoxic and anti-inflammatory effects of ZOE cement during setting in two-dimensional (2D) or three-dimensional (3D) cultures of immortalized human oral keratinocytes (IHOKs) with determining the extract components responsible for these effects. Methods Extracts of mixed ZOE at different stages of setting were analyzed by a digital pH meter, ICP-MS, and GC-MS. Serial concentrations of extract and their mixture of ZnCl2, ZnSO4·H2O, and eugenol liquid were added to the 2D and 3D IHOK cultures to determine the half maximal effective concentration in investigating the cause of cytotoxicity by means of WST assay and to investigate mRNA expression levels of inflammatory cytokines by RT-PCR. Results Zn2+ and eugenol (4-19 ppm) were detected in the extracts. In the early setting stage, significant cytotoxicity was observed in the 2D and 3D IHOK cultures (P < 0.05). The EC50 of Zn2+ from ZnCl2 was 5-44 ppm in both cultures, whereas the EC50 of eugenol was not detectable under 100 ppm. Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn2+ alone and treatment of the 3D IHOKs with Zn2+ plus eugenol resulted in significantly lower expression levels of IL-1β, IL-6, and IL-8 (P < 0.05). Significance The cytotoxic effect of ZOE on IHOKs was greater during the setting stage owing to the presence of Zn2+. The anti-inflammatory response to ZOE was induced by a combination of Zn2+ and eugenol. Cytotoxic and anti-inflammatory effects differed between the 2D and 3D IHOK cultures.

Original languageEnglish
Pages (from-to)e93-e104
JournalDental Materials
Volume32
Issue number5
DOIs
Publication statusPublished - 2016 May 1

Fingerprint

Eugenol
Cytotoxicity
Keratinocytes
Zinc
Anti-Inflammatory Agents
Ions
pH meters
Cytokines
Interleukin-8
Interleukin-1
Gene expression
Interleukin-6
Assays
Cements
Gene Expression
Polymerase Chain Reaction
Messenger RNA
Liquids

All Science Journal Classification (ASJC) codes

  • Materials Science(all)
  • Dentistry(all)
  • Mechanics of Materials

Cite this

@article{6684ba24bbef4ceda8e34e63806475ac,
title = "Cytotoxicity and anti-inflammatory effects of zinc ions and eugenol during setting of ZOE in immortalized human oral keratinocytes grown as three-dimensional spheroids",
abstract = "Objectives The objective of this study is to assess the cytotoxic and anti-inflammatory effects of ZOE cement during setting in two-dimensional (2D) or three-dimensional (3D) cultures of immortalized human oral keratinocytes (IHOKs) with determining the extract components responsible for these effects. Methods Extracts of mixed ZOE at different stages of setting were analyzed by a digital pH meter, ICP-MS, and GC-MS. Serial concentrations of extract and their mixture of ZnCl2, ZnSO4·H2O, and eugenol liquid were added to the 2D and 3D IHOK cultures to determine the half maximal effective concentration in investigating the cause of cytotoxicity by means of WST assay and to investigate mRNA expression levels of inflammatory cytokines by RT-PCR. Results Zn2+ and eugenol (4-19 ppm) were detected in the extracts. In the early setting stage, significant cytotoxicity was observed in the 2D and 3D IHOK cultures (P < 0.05). The EC50 of Zn2+ from ZnCl2 was 5-44 ppm in both cultures, whereas the EC50 of eugenol was not detectable under 100 ppm. Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn2+ alone and treatment of the 3D IHOKs with Zn2+ plus eugenol resulted in significantly lower expression levels of IL-1β, IL-6, and IL-8 (P < 0.05). Significance The cytotoxic effect of ZOE on IHOKs was greater during the setting stage owing to the presence of Zn2+. The anti-inflammatory response to ZOE was induced by a combination of Zn2+ and eugenol. Cytotoxic and anti-inflammatory effects differed between the 2D and 3D IHOK cultures.",
author = "Lee, {Jung Hwan} and Lee, {Hae Hyoung} and Kim, {Kyoung Nam} and Kim, {Kwang Mahn}",
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Cytotoxicity and anti-inflammatory effects of zinc ions and eugenol during setting of ZOE in immortalized human oral keratinocytes grown as three-dimensional spheroids. / Lee, Jung Hwan; Lee, Hae Hyoung; Kim, Kyoung Nam; Kim, Kwang Mahn.

In: Dental Materials, Vol. 32, No. 5, 01.05.2016, p. e93-e104.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Cytotoxicity and anti-inflammatory effects of zinc ions and eugenol during setting of ZOE in immortalized human oral keratinocytes grown as three-dimensional spheroids

AU - Lee, Jung Hwan

AU - Lee, Hae Hyoung

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AU - Kim, Kwang Mahn

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N2 - Objectives The objective of this study is to assess the cytotoxic and anti-inflammatory effects of ZOE cement during setting in two-dimensional (2D) or three-dimensional (3D) cultures of immortalized human oral keratinocytes (IHOKs) with determining the extract components responsible for these effects. Methods Extracts of mixed ZOE at different stages of setting were analyzed by a digital pH meter, ICP-MS, and GC-MS. Serial concentrations of extract and their mixture of ZnCl2, ZnSO4·H2O, and eugenol liquid were added to the 2D and 3D IHOK cultures to determine the half maximal effective concentration in investigating the cause of cytotoxicity by means of WST assay and to investigate mRNA expression levels of inflammatory cytokines by RT-PCR. Results Zn2+ and eugenol (4-19 ppm) were detected in the extracts. In the early setting stage, significant cytotoxicity was observed in the 2D and 3D IHOK cultures (P < 0.05). The EC50 of Zn2+ from ZnCl2 was 5-44 ppm in both cultures, whereas the EC50 of eugenol was not detectable under 100 ppm. Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn2+ alone and treatment of the 3D IHOKs with Zn2+ plus eugenol resulted in significantly lower expression levels of IL-1β, IL-6, and IL-8 (P < 0.05). Significance The cytotoxic effect of ZOE on IHOKs was greater during the setting stage owing to the presence of Zn2+. The anti-inflammatory response to ZOE was induced by a combination of Zn2+ and eugenol. Cytotoxic and anti-inflammatory effects differed between the 2D and 3D IHOK cultures.

AB - Objectives The objective of this study is to assess the cytotoxic and anti-inflammatory effects of ZOE cement during setting in two-dimensional (2D) or three-dimensional (3D) cultures of immortalized human oral keratinocytes (IHOKs) with determining the extract components responsible for these effects. Methods Extracts of mixed ZOE at different stages of setting were analyzed by a digital pH meter, ICP-MS, and GC-MS. Serial concentrations of extract and their mixture of ZnCl2, ZnSO4·H2O, and eugenol liquid were added to the 2D and 3D IHOK cultures to determine the half maximal effective concentration in investigating the cause of cytotoxicity by means of WST assay and to investigate mRNA expression levels of inflammatory cytokines by RT-PCR. Results Zn2+ and eugenol (4-19 ppm) were detected in the extracts. In the early setting stage, significant cytotoxicity was observed in the 2D and 3D IHOK cultures (P < 0.05). The EC50 of Zn2+ from ZnCl2 was 5-44 ppm in both cultures, whereas the EC50 of eugenol was not detectable under 100 ppm. Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn2+ alone and treatment of the 3D IHOKs with Zn2+ plus eugenol resulted in significantly lower expression levels of IL-1β, IL-6, and IL-8 (P < 0.05). Significance The cytotoxic effect of ZOE on IHOKs was greater during the setting stage owing to the presence of Zn2+. The anti-inflammatory response to ZOE was induced by a combination of Zn2+ and eugenol. Cytotoxic and anti-inflammatory effects differed between the 2D and 3D IHOK cultures.

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