Source:http://linkedlifedata.com/resource/pubmed/id/15919110
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
31
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pubmed:dateCreated |
2005-6-20
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pubmed:abstractText |
Recent studies have revealed that visible-light (VL)-irradiated camphorquinone (CQ), in the presence of a tertiary amine (e.g., N,N-dimethyl-p-toluidine, DMT), generates initiating radicals that may indiscriminately react with molecular oxygen forming reactive oxygen species (ROS). In this study, the ability of the antioxidants N-acetyl-l-cysteine (NAC) and ascorbic acid (AA) to reduce intracellular oxidative stress induced by VL-irradiated CQ/DMT or VL-irradiated hydrogen peroxide (H(2)O(2)) was assessed in an immortalized Murine cementoblast cell line (OCCM.30) and an immortalized Murine fibroblast cell line, 3T3-Swiss albino (3T3). Intracellular oxidative stress was measured with the membrane permeable dye, 2',7'-dichlorodihydrofluorescein diacetate (H(2)DCF-DA). VL-irradiated CQ/DMT and VL-irradiated H(2)O(2) each produced significantly (p<0.001) elevated intracellular oxidative levels in both cell types compared to intracellular ROS levels in VL-irradiated untreated cells. OCCM.30 cementoblasts were found to be almost twice as sensitive to VL-irradiated CQ/DMT and VL-irradiated H(2)O(2) treatment compared to 3T3 fibroblasts. Furthermore, 10mm NAC and 10mm AA each eliminated oxidative stress induced by VL-irradiated CQ/DMT and VL-irradiated H(2)O(2) in both cell types. Our results suggest that NAC and AA may effectively reduce or eliminate oxidative stress in cells exposed to VL-irradiated CQ/DMT following polymerization.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetylcysteine,
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Composite Resins,
http://linkedlifedata.com/resource/pubmed/chemical/Dental Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species,
http://linkedlifedata.com/resource/pubmed/chemical/Terpenes,
http://linkedlifedata.com/resource/pubmed/chemical/camphoroquinone
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0142-9612
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6136-42
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15919110-3T3 Cells,
pubmed-meshheading:15919110-Acetylcysteine,
pubmed-meshheading:15919110-Animals,
pubmed-meshheading:15919110-Ascorbic Acid,
pubmed-meshheading:15919110-Cell Line,
pubmed-meshheading:15919110-Composite Resins,
pubmed-meshheading:15919110-Dental Cementum,
pubmed-meshheading:15919110-Dental Materials,
pubmed-meshheading:15919110-Drug Interactions,
pubmed-meshheading:15919110-Light,
pubmed-meshheading:15919110-Mice,
pubmed-meshheading:15919110-Oxidative Stress,
pubmed-meshheading:15919110-Reactive Oxygen Species,
pubmed-meshheading:15919110-Terpenes
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pubmed:year |
2005
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pubmed:articleTitle |
The effect of N-acetyl-l-cysteine and ascorbic acid on visible-light-irradiated camphorquinone/N,N-dimethyl-p-toluidine-induced oxidative stress in two immortalized cell lines.
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pubmed:affiliation |
Department of Restorative Dentistry/Division of Operative Dentistry, School of Dentistry, University of Washington, Box 357456, Seattle, WA, 98195-7456 USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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