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Induction of cytotoxicity, oxidative stress and genotoxicity by root filling pastes used in primary teeth

Aim To evaluate the cytotoxicity, oxidative stress and genotoxicity in vitro of four iodoform pastes and three calcium hydroxide pastes. Methodology Peripheral blood mononuclear cells (PBMCs) and pure calf thymus DNA (dsDNA) were exposed to extracts of the pastes. Cytotoxicity was assessed with the...

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Published in:International endodontic journal 2016-08, Vol.49 (8), p.737-745
Main Authors: Pires, C. W., Botton, G., Cadoná, F. C., Machado, A. K., Azzolin, V. F., da Cruz, I. B. M., Sagrillo, M. R., Praetzel, J. R.
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container_issue 8
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container_title International endodontic journal
container_volume 49
creator Pires, C. W.
Botton, G.
Cadoná, F. C.
Machado, A. K.
Azzolin, V. F.
da Cruz, I. B. M.
Sagrillo, M. R.
Praetzel, J. R.
description Aim To evaluate the cytotoxicity, oxidative stress and genotoxicity in vitro of four iodoform pastes and three calcium hydroxide pastes. Methodology Peripheral blood mononuclear cells (PBMCs) and pure calf thymus DNA (dsDNA) were exposed to extracts of the pastes. Cytotoxicity was assessed with the MTT assay. Generation of reactive oxygen species (ROS) was evaluated using a DCFH‐DA assay, and lipid peroxidation was evaluated using a TBARS assay. Genotoxicity was evaluated using the alkaline comet assay and Genomodifier capacity assay (GEMO). All tests were performed after 24 h and 72 h of cell exposure, except GEMO. After performing the Kolmogorov–Smirnov test, data were analysed by Kruskal–Wallis and Dunn's post‐tests, and anova with Dunnett's post‐test, with a significance level established at P 
doi_str_mv 10.1111/iej.12502
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W. ; Botton, G. ; Cadoná, F. C. ; Machado, A. K. ; Azzolin, V. F. ; da Cruz, I. B. M. ; Sagrillo, M. R. ; Praetzel, J. R.</creator><creatorcontrib>Pires, C. W. ; Botton, G. ; Cadoná, F. C. ; Machado, A. K. ; Azzolin, V. F. ; da Cruz, I. B. M. ; Sagrillo, M. R. ; Praetzel, J. R.</creatorcontrib><description><![CDATA[Aim To evaluate the cytotoxicity, oxidative stress and genotoxicity in vitro of four iodoform pastes and three calcium hydroxide pastes. Methodology Peripheral blood mononuclear cells (PBMCs) and pure calf thymus DNA (dsDNA) were exposed to extracts of the pastes. Cytotoxicity was assessed with the MTT assay. Generation of reactive oxygen species (ROS) was evaluated using a DCFH‐DA assay, and lipid peroxidation was evaluated using a TBARS assay. Genotoxicity was evaluated using the alkaline comet assay and Genomodifier capacity assay (GEMO). All tests were performed after 24 h and 72 h of cell exposure, except GEMO. After performing the Kolmogorov–Smirnov test, data were analysed by Kruskal–Wallis and Dunn's post‐tests, and anova with Dunnett's post‐test, with a significance level established at P < 0.05. Results The MTT assay revealed that chlorhexidine, Maxitrol and neomycin sulphate + bacitracin pastes decreased cell viability after 24 h (P < 0.05). No group was associated with a significant decreased cell viability or lipid peroxidation after 72 h. Calcium hydroxide pastes increased the cell viability levels at both experimental times (P < 0.05). Lipid peroxidation was observed with the exposure of cells to calcium hydroxide pastes after 24 h (P < 0.05). Exposure to chlorhexidine, Guedes‐Pinto and calcium hydroxide pastes resulted in a significant increase in ROS after 24 h (P < 0.05), whereas iodoform pastes and Calen thickened with zinc oxide significantly increased the ROS after 72 h (P < 0.05). The comet assay revealed that exposure of the PBMCs to iodoform pastes did not damage DNA at either period of time (P > 0.05). However, chlorhexidine paste caused DNA damage in dsDNA (P < 0.05). Calcium hydroxide pastes caused DNA damage in both tests (P < 0.05). Conclusion The pastes varied in their ability to induce cytotoxicity, genotoxicity and oxidative stress. In general, Guedes‐Pinto, Maxitrol and neomycin sulphate + bacitracin pastes exhibited better biocompatibility in vitro.]]></description><identifier>ISSN: 0143-2885</identifier><identifier>EISSN: 1365-2591</identifier><identifier>DOI: 10.1111/iej.12502</identifier><identifier>PMID: 26174479</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Analysis of Variance ; Animals ; biocompatibility ; calcium hydroxide ; Cattle ; deciduous tooth ; Dentistry ; DNA - drug effects ; DNA Damage ; Humans ; Hydrocarbons, Iodinated - pharmacology ; iodoform ; Leukocytes, Mononuclear - drug effects ; Leukocytes, Mononuclear - metabolism ; Materials Testing ; Oxidative Stress - drug effects ; pulpectomy ; Reactive Oxygen Species - metabolism ; root canal filling materials ; Root Canal Filling Materials - pharmacology ; Statistics, Nonparametric ; Tooth, Deciduous ; Toxicity Tests</subject><ispartof>International endodontic journal, 2016-08, Vol.49 (8), p.737-745</ispartof><rights>2015 International Endodontic Journal. Published by John Wiley &amp; Sons Ltd</rights><rights>2015 International Endodontic Journal. Published by John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5032-dcd466907f4b4b66064f3d1ca43e147fbf367e27a2972c9d2247e502fd5e8ed53</citedby><cites>FETCH-LOGICAL-c5032-dcd466907f4b4b66064f3d1ca43e147fbf367e27a2972c9d2247e502fd5e8ed53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26174479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pires, C. W.</creatorcontrib><creatorcontrib>Botton, G.</creatorcontrib><creatorcontrib>Cadoná, F. C.</creatorcontrib><creatorcontrib>Machado, A. K.</creatorcontrib><creatorcontrib>Azzolin, V. F.</creatorcontrib><creatorcontrib>da Cruz, I. B. M.</creatorcontrib><creatorcontrib>Sagrillo, M. R.</creatorcontrib><creatorcontrib>Praetzel, J. R.</creatorcontrib><title>Induction of cytotoxicity, oxidative stress and genotoxicity by root filling pastes used in primary teeth</title><title>International endodontic journal</title><addtitle>Int Endod J</addtitle><description><![CDATA[Aim To evaluate the cytotoxicity, oxidative stress and genotoxicity in vitro of four iodoform pastes and three calcium hydroxide pastes. Methodology Peripheral blood mononuclear cells (PBMCs) and pure calf thymus DNA (dsDNA) were exposed to extracts of the pastes. Cytotoxicity was assessed with the MTT assay. Generation of reactive oxygen species (ROS) was evaluated using a DCFH‐DA assay, and lipid peroxidation was evaluated using a TBARS assay. Genotoxicity was evaluated using the alkaline comet assay and Genomodifier capacity assay (GEMO). All tests were performed after 24 h and 72 h of cell exposure, except GEMO. After performing the Kolmogorov–Smirnov test, data were analysed by Kruskal–Wallis and Dunn's post‐tests, and anova with Dunnett's post‐test, with a significance level established at P < 0.05. Results The MTT assay revealed that chlorhexidine, Maxitrol and neomycin sulphate + bacitracin pastes decreased cell viability after 24 h (P < 0.05). No group was associated with a significant decreased cell viability or lipid peroxidation after 72 h. Calcium hydroxide pastes increased the cell viability levels at both experimental times (P < 0.05). Lipid peroxidation was observed with the exposure of cells to calcium hydroxide pastes after 24 h (P < 0.05). Exposure to chlorhexidine, Guedes‐Pinto and calcium hydroxide pastes resulted in a significant increase in ROS after 24 h (P < 0.05), whereas iodoform pastes and Calen thickened with zinc oxide significantly increased the ROS after 72 h (P < 0.05). The comet assay revealed that exposure of the PBMCs to iodoform pastes did not damage DNA at either period of time (P > 0.05). However, chlorhexidine paste caused DNA damage in dsDNA (P < 0.05). Calcium hydroxide pastes caused DNA damage in both tests (P < 0.05). Conclusion The pastes varied in their ability to induce cytotoxicity, genotoxicity and oxidative stress. In general, Guedes‐Pinto, Maxitrol and neomycin sulphate + bacitracin pastes exhibited better biocompatibility in vitro.]]></description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>biocompatibility</subject><subject>calcium hydroxide</subject><subject>Cattle</subject><subject>deciduous tooth</subject><subject>Dentistry</subject><subject>DNA - drug effects</subject><subject>DNA Damage</subject><subject>Humans</subject><subject>Hydrocarbons, Iodinated - pharmacology</subject><subject>iodoform</subject><subject>Leukocytes, Mononuclear - drug effects</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Materials Testing</subject><subject>Oxidative Stress - drug effects</subject><subject>pulpectomy</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>root canal filling materials</subject><subject>Root Canal Filling Materials - pharmacology</subject><subject>Statistics, Nonparametric</subject><subject>Tooth, Deciduous</subject><subject>Toxicity Tests</subject><issn>0143-2885</issn><issn>1365-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kE1v1DAQhi0EokvhwB9APoJEWn97c0RVWxZVRUit2pvl2OPiko2X2Gmbf49ht3tjLjOHZ17NPAi9p-SI1jqOcH9EmSTsBVpQrmTDZEtfogWhgjdsuZQH6E3O94QQSTh9jQ6YoloI3S5QXA1-ciWmAaeA3VxSSU_RxTJ_xnXwtsQHwLmMkDO2g8d3MOwR3M14TKngEPs-Dnd4Y3OBjKcMHscBb8a4tuOMC0D5-Ra9CrbP8G7XD9H12enVydfm4vv56uTLRePqcazxzgulWqKD6ESnFFEicE-dFRyo0KELXGlg2rJWM9d6xoSG-nrwEpbgJT9EH7e5mzH9niAXs47ZQd_bAdKUDV0SrlsuKavopy3qxpTzCMHsLjaUmL9mTTVr_pmt7Idd7NStwe_JZ5UVON4Cj7GH-f9JZnX67Tmy2W7Eau1pv2HHX0ZprqW5uTw34sctu7xqz8wN_wNT2pMc</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Pires, C. W.</creator><creator>Botton, G.</creator><creator>Cadoná, F. C.</creator><creator>Machado, A. K.</creator><creator>Azzolin, V. F.</creator><creator>da Cruz, I. B. M.</creator><creator>Sagrillo, M. R.</creator><creator>Praetzel, J. R.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201608</creationdate><title>Induction of cytotoxicity, oxidative stress and genotoxicity by root filling pastes used in primary teeth</title><author>Pires, C. W. ; Botton, G. ; Cadoná, F. C. ; Machado, A. K. ; Azzolin, V. F. ; da Cruz, I. B. M. ; Sagrillo, M. R. ; Praetzel, J. 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W.</creatorcontrib><creatorcontrib>Botton, G.</creatorcontrib><creatorcontrib>Cadoná, F. C.</creatorcontrib><creatorcontrib>Machado, A. K.</creatorcontrib><creatorcontrib>Azzolin, V. F.</creatorcontrib><creatorcontrib>da Cruz, I. B. M.</creatorcontrib><creatorcontrib>Sagrillo, M. R.</creatorcontrib><creatorcontrib>Praetzel, J. R.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International endodontic journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pires, C. W.</au><au>Botton, G.</au><au>Cadoná, F. C.</au><au>Machado, A. K.</au><au>Azzolin, V. F.</au><au>da Cruz, I. B. M.</au><au>Sagrillo, M. R.</au><au>Praetzel, J. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of cytotoxicity, oxidative stress and genotoxicity by root filling pastes used in primary teeth</atitle><jtitle>International endodontic journal</jtitle><addtitle>Int Endod J</addtitle><date>2016-08</date><risdate>2016</risdate><volume>49</volume><issue>8</issue><spage>737</spage><epage>745</epage><pages>737-745</pages><issn>0143-2885</issn><eissn>1365-2591</eissn><abstract><![CDATA[Aim To evaluate the cytotoxicity, oxidative stress and genotoxicity in vitro of four iodoform pastes and three calcium hydroxide pastes. Methodology Peripheral blood mononuclear cells (PBMCs) and pure calf thymus DNA (dsDNA) were exposed to extracts of the pastes. Cytotoxicity was assessed with the MTT assay. Generation of reactive oxygen species (ROS) was evaluated using a DCFH‐DA assay, and lipid peroxidation was evaluated using a TBARS assay. Genotoxicity was evaluated using the alkaline comet assay and Genomodifier capacity assay (GEMO). All tests were performed after 24 h and 72 h of cell exposure, except GEMO. After performing the Kolmogorov–Smirnov test, data were analysed by Kruskal–Wallis and Dunn's post‐tests, and anova with Dunnett's post‐test, with a significance level established at P < 0.05. Results The MTT assay revealed that chlorhexidine, Maxitrol and neomycin sulphate + bacitracin pastes decreased cell viability after 24 h (P < 0.05). No group was associated with a significant decreased cell viability or lipid peroxidation after 72 h. Calcium hydroxide pastes increased the cell viability levels at both experimental times (P < 0.05). Lipid peroxidation was observed with the exposure of cells to calcium hydroxide pastes after 24 h (P < 0.05). Exposure to chlorhexidine, Guedes‐Pinto and calcium hydroxide pastes resulted in a significant increase in ROS after 24 h (P < 0.05), whereas iodoform pastes and Calen thickened with zinc oxide significantly increased the ROS after 72 h (P < 0.05). The comet assay revealed that exposure of the PBMCs to iodoform pastes did not damage DNA at either period of time (P > 0.05). However, chlorhexidine paste caused DNA damage in dsDNA (P < 0.05). Calcium hydroxide pastes caused DNA damage in both tests (P < 0.05). Conclusion The pastes varied in their ability to induce cytotoxicity, genotoxicity and oxidative stress. In general, Guedes‐Pinto, Maxitrol and neomycin sulphate + bacitracin pastes exhibited better biocompatibility in vitro.]]></abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26174479</pmid><doi>10.1111/iej.12502</doi><tpages>9</tpages></addata></record>
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ispartof International endodontic journal, 2016-08, Vol.49 (8), p.737-745
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source Wiley-Blackwell Read & Publish Collection
subjects Analysis of Variance
Animals
biocompatibility
calcium hydroxide
Cattle
deciduous tooth
Dentistry
DNA - drug effects
DNA Damage
Humans
Hydrocarbons, Iodinated - pharmacology
iodoform
Leukocytes, Mononuclear - drug effects
Leukocytes, Mononuclear - metabolism
Materials Testing
Oxidative Stress - drug effects
pulpectomy
Reactive Oxygen Species - metabolism
root canal filling materials
Root Canal Filling Materials - pharmacology
Statistics, Nonparametric
Tooth, Deciduous
Toxicity Tests
title Induction of cytotoxicity, oxidative stress and genotoxicity by root filling pastes used in primary teeth
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