Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production

Detalhes bibliográficos
Autor(a) principal: Oliveira,Luciane Dias de
Data de Publicação: 2022
Outros Autores: Oliveira,Felipe Eduardo de, Hatje,Bárbara Araujo, Valera,Marcia Carneiro, Carvalho,Cláudio Antonio Talge, Hasna,Amjad Abu
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Dental Journal
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402022000600036
Resumo: Abstract The aim of this study was to evaluate in vitro the effect of calcium hydroxide [Ca(OH)2], 2% chlorhexidine gel (CHX) on macrophages (RAW 264.7) to produce pro-inflammatory cytokines and nitric oxide after pretreatment with lipoteichoic acid (LTA) of Enterococcus faecalis. Forty-eight human single-rooted teeth were instrumented with R25.08 (RECIPROC) and sterilized by gamma irradiation. LTA was inoculated in the root canal of each specimen for 96 hours. Specimens were instrumented with 40.06 and 50.05 (RECIPROC) and medicated with: I) Pyrogen-free saline solution (SS); II) 2% CHX gel; III) Ca(OH)2 + SS; or IV) Ca(OH)2 + CHX for 14 days. Three samples (S) were performed of the root canal of each specimen at: S1) immediately after instrumentation; S2) after Ethylenediaminetetraacetic acid (EDTA); S3) after intracanal medication removal. Subsequent quantification of cytokines (IL-1β, TNF-α, MIP-1α, IP-10, G-CSF and IL-6) by immunosorbent assay (ELISA) and nitric oxide by the Griess method was carried-out. Data were submitted to a normality test and then analyzed with one-way ANOVA and Tukey test with a significance level of 5% using GraphPad Prism 6. Ca(OH)2 + SS and Ca(OH)2 + CHX presented lower levels of TNF-α, TNF-α, IL-6, G-CSF and nitric oxide. Ca(OH)2 + SS was the most effective in reducing MIP-1α. CHX was effective in reducing IL-6 and G-CSF. Therefore, the combined intracanal medication of calcium hydroxide and chlorhexidine is effective in reducing the cytokines TNF-α, IL-1β, IL-6, G-CSF and nitric oxide.
id FUNORP-1_9e376bb8d8260e832d342fe31a5e23a9
oai_identifier_str oai:scielo:S0103-64402022000600036
network_acronym_str FUNORP-1
network_name_str Brazilian Dental Journal
repository_id_str
spelling Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines productionlipoteichoic acidcytokinesmacrophagescalcium hydroxidechlorhexidineAbstract The aim of this study was to evaluate in vitro the effect of calcium hydroxide [Ca(OH)2], 2% chlorhexidine gel (CHX) on macrophages (RAW 264.7) to produce pro-inflammatory cytokines and nitric oxide after pretreatment with lipoteichoic acid (LTA) of Enterococcus faecalis. Forty-eight human single-rooted teeth were instrumented with R25.08 (RECIPROC) and sterilized by gamma irradiation. LTA was inoculated in the root canal of each specimen for 96 hours. Specimens were instrumented with 40.06 and 50.05 (RECIPROC) and medicated with: I) Pyrogen-free saline solution (SS); II) 2% CHX gel; III) Ca(OH)2 + SS; or IV) Ca(OH)2 + CHX for 14 days. Three samples (S) were performed of the root canal of each specimen at: S1) immediately after instrumentation; S2) after Ethylenediaminetetraacetic acid (EDTA); S3) after intracanal medication removal. Subsequent quantification of cytokines (IL-1β, TNF-α, MIP-1α, IP-10, G-CSF and IL-6) by immunosorbent assay (ELISA) and nitric oxide by the Griess method was carried-out. Data were submitted to a normality test and then analyzed with one-way ANOVA and Tukey test with a significance level of 5% using GraphPad Prism 6. Ca(OH)2 + SS and Ca(OH)2 + CHX presented lower levels of TNF-α, TNF-α, IL-6, G-CSF and nitric oxide. Ca(OH)2 + SS was the most effective in reducing MIP-1α. CHX was effective in reducing IL-6 and G-CSF. Therefore, the combined intracanal medication of calcium hydroxide and chlorhexidine is effective in reducing the cytokines TNF-α, IL-1β, IL-6, G-CSF and nitric oxide.Fundação Odontológica de Ribeirão Preto2022-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402022000600036Brazilian Dental Journal v.33 n.6 2022reponame:Brazilian Dental Journalinstname:Fundação Odontológica de Ribeirão Preto (FUNORP)instacron:FUNORP10.1590/0103-6440202205195info:eu-repo/semantics/openAccessOliveira,Luciane Dias deOliveira,Felipe Eduardo deHatje,Bárbara AraujoValera,Marcia CarneiroCarvalho,Cláudio Antonio TalgeHasna,Amjad Abueng2022-12-01T00:00:00Zoai:scielo:S0103-64402022000600036Revistahttps://www.scielo.br/j/bdj/https://old.scielo.br/oai/scielo-oai.phpbdj@forp.usp.br||sergio@fosjc.unesp.br1806-47600103-6440opendoar:2022-12-01T00:00Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)false
dc.title.none.fl_str_mv Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
title Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
spellingShingle Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
Oliveira,Luciane Dias de
lipoteichoic acid
cytokines
macrophages
calcium hydroxide
chlorhexidine
title_short Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
title_full Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
title_fullStr Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
title_full_unstemmed Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
title_sort Detoxification of LTA by intracanal medication: analysis by macrophages proinflammatory cytokines production
author Oliveira,Luciane Dias de
author_facet Oliveira,Luciane Dias de
Oliveira,Felipe Eduardo de
Hatje,Bárbara Araujo
Valera,Marcia Carneiro
Carvalho,Cláudio Antonio Talge
Hasna,Amjad Abu
author_role author
author2 Oliveira,Felipe Eduardo de
Hatje,Bárbara Araujo
Valera,Marcia Carneiro
Carvalho,Cláudio Antonio Talge
Hasna,Amjad Abu
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira,Luciane Dias de
Oliveira,Felipe Eduardo de
Hatje,Bárbara Araujo
Valera,Marcia Carneiro
Carvalho,Cláudio Antonio Talge
Hasna,Amjad Abu
dc.subject.por.fl_str_mv lipoteichoic acid
cytokines
macrophages
calcium hydroxide
chlorhexidine
topic lipoteichoic acid
cytokines
macrophages
calcium hydroxide
chlorhexidine
description Abstract The aim of this study was to evaluate in vitro the effect of calcium hydroxide [Ca(OH)2], 2% chlorhexidine gel (CHX) on macrophages (RAW 264.7) to produce pro-inflammatory cytokines and nitric oxide after pretreatment with lipoteichoic acid (LTA) of Enterococcus faecalis. Forty-eight human single-rooted teeth were instrumented with R25.08 (RECIPROC) and sterilized by gamma irradiation. LTA was inoculated in the root canal of each specimen for 96 hours. Specimens were instrumented with 40.06 and 50.05 (RECIPROC) and medicated with: I) Pyrogen-free saline solution (SS); II) 2% CHX gel; III) Ca(OH)2 + SS; or IV) Ca(OH)2 + CHX for 14 days. Three samples (S) were performed of the root canal of each specimen at: S1) immediately after instrumentation; S2) after Ethylenediaminetetraacetic acid (EDTA); S3) after intracanal medication removal. Subsequent quantification of cytokines (IL-1β, TNF-α, MIP-1α, IP-10, G-CSF and IL-6) by immunosorbent assay (ELISA) and nitric oxide by the Griess method was carried-out. Data were submitted to a normality test and then analyzed with one-way ANOVA and Tukey test with a significance level of 5% using GraphPad Prism 6. Ca(OH)2 + SS and Ca(OH)2 + CHX presented lower levels of TNF-α, TNF-α, IL-6, G-CSF and nitric oxide. Ca(OH)2 + SS was the most effective in reducing MIP-1α. CHX was effective in reducing IL-6 and G-CSF. Therefore, the combined intracanal medication of calcium hydroxide and chlorhexidine is effective in reducing the cytokines TNF-α, IL-1β, IL-6, G-CSF and nitric oxide.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402022000600036
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-64402022000600036
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/0103-6440202205195
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Fundação Odontológica de Ribeirão Preto
publisher.none.fl_str_mv Fundação Odontológica de Ribeirão Preto
dc.source.none.fl_str_mv Brazilian Dental Journal v.33 n.6 2022
reponame:Brazilian Dental Journal
instname:Fundação Odontológica de Ribeirão Preto (FUNORP)
instacron:FUNORP
instname_str Fundação Odontológica de Ribeirão Preto (FUNORP)
instacron_str FUNORP
institution FUNORP
reponame_str Brazilian Dental Journal
collection Brazilian Dental Journal
repository.name.fl_str_mv Brazilian Dental Journal - Fundação Odontológica de Ribeirão Preto (FUNORP)
repository.mail.fl_str_mv bdj@forp.usp.br||sergio@fosjc.unesp.br
_version_ 1754204096720535552