2010
DOI: 10.1016/j.biomaterials.2010.07.049
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The role of reactive oxygen species and hemeoxygenase-1 expression in the cytotoxicity, cell cycle alteration and apoptosis of dental pulp cells induced by BisGMA

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Cited by 85 publications
(96 citation statements)
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References 35 publications
(74 reference statements)
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“…TEGDMA in its unreacted monomer form is relatively hydrophilic and shows greater water solubility potential than most other commonly used monomer components, so that it is more easily eluted from an RBC material in comparison to other monomers like Bis-GMA for example [37]. TEGDMA in particular may have toxic effects on oral tissue cells like gingival or pulp cells [38] and may cause genotoxicity and changes in cytokine expression [39]. Moreover, TEGDMA as its chemical precursor is assumed to be disseminated systemically via salivary-intestinal or pulp-tissue circulation pathways to be metabolized in other inner organs [36].…”
Section: Discussionmentioning
confidence: 98%
“…TEGDMA in its unreacted monomer form is relatively hydrophilic and shows greater water solubility potential than most other commonly used monomer components, so that it is more easily eluted from an RBC material in comparison to other monomers like Bis-GMA for example [37]. TEGDMA in particular may have toxic effects on oral tissue cells like gingival or pulp cells [38] and may cause genotoxicity and changes in cytokine expression [39]. Moreover, TEGDMA as its chemical precursor is assumed to be disseminated systemically via salivary-intestinal or pulp-tissue circulation pathways to be metabolized in other inner organs [36].…”
Section: Discussionmentioning
confidence: 98%
“…As the CLSM method can sensitively give the initial rate of viable cells, other possibilities could be foreseen to assess more endpoints. In particular, as it has been recently reported that composite monomers affect cells through reactive oxygen species (ROS) [46][47][48] , further investigation is needed to assess correlations if any between cytotoxicity signaling networks and ROS production. The future protocol could be designed to simultaneously evaluate ROS production (H 2 O 2 and/or O 2 -staining) and cytotoxicity ratio (Live/dead staining) using time lapse CLSM imaging.…”
Section: Discussionmentioning
confidence: 99%
“…Flow cytometric analysis was performed as described previously [26]. Briefly, EAHY cells (5 x 10 5 cells) were exposed to various concentrations of arecoline for 24 h. Then, both floating and attached cells were collected and centrifuged in tubes.…”
Section: Flow Cytometric Analysis Of Cell Cycle Distribution Of Eahy mentioning
confidence: 99%