In vitro inflammatory modulation of bioceramic endodontic sealer in macrophages stimulated by bacterial lipopolysaccharide

Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS). Methodology After initial setting, the sealers were conditioned with s...

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Published inInternational endodontic journal Vol. 56; no. 2; pp. 213 - 226
Main Authors Martorano, Antônio Secco, Messias, Nadyne Saab, Bighetti‐Trevisan, Rayana Longo, Oliveira, Paulo Tambasco, Castro Raucci, Larissa Moreira Spinola, Raucci Neto, Walter
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.02.2023
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Abstract Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS). Methodology After initial setting, the sealers were conditioned with serum‐free culture medium for 24 h (1 ml/cm2). Macrophages from the RAW 264.7 strain were exposed to sealer extracts in a 1:16 ratio in a culture medium with or without LPS. Cell morphology, viability, mitochondrial activity, oxidative stress and gene expression of interleukin 1β (IL‐1β) and tumour necrosis factor‐alpha (TNF‐α) were evaluated. Data on mitochondrial activity, oxidative stress and TNF‐α were analysed using a two‐way analysis of variance (anova) test, followed by the Student–Newman–Keuls post‐test. IL‐1β data were analysed using one‐way anova, followed by SNK, and the t‐test was used for intragroup comparison. The significance level was set at 5%. Results In the absence of LPS, only AH Plus and Sealer 26 showed a reduction in cell density, while in the presence of LPS, Sealer 26 had the lowest density compared to the other groups. In terms of mitochondrial activity, at 24 and 48 h, Sealer Plus BC had significantly higher mean values than Sealer 26 and AH Plus (p < .05). Sealer 26 exhibited the lowest levels of oxidative stress and IL‐1β and TNF‐α expression, regardless of the presence of LPS (p < .05). Conclusions Although all sealers interfere with the response of macrophages to LPS, contact with epoxy resin‐based sealers can impair cell activity in vitro, while bioceramic sealer seems to favour the inflammatory functions of these cells.
AbstractList AimTo evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS).MethodologyAfter initial setting, the sealers were conditioned with serum‐free culture medium for 24 h (1 ml/cm2). Macrophages from the RAW 264.7 strain were exposed to sealer extracts in a 1:16 ratio in a culture medium with or without LPS. Cell morphology, viability, mitochondrial activity, oxidative stress and gene expression of interleukin 1β (IL‐1β) and tumour necrosis factor‐alpha (TNF‐α) were evaluated. Data on mitochondrial activity, oxidative stress and TNF‐α were analysed using a two‐way analysis of variance (anova) test, followed by the Student–Newman–Keuls post‐test. IL‐1β data were analysed using one‐way anova, followed by SNK, and the t‐test was used for intragroup comparison. The significance level was set at 5%.ResultsIn the absence of LPS, only AH Plus and Sealer 26 showed a reduction in cell density, while in the presence of LPS, Sealer 26 had the lowest density compared to the other groups. In terms of mitochondrial activity, at 24 and 48 h, Sealer Plus BC had significantly higher mean values than Sealer 26 and AH Plus (p < .05). Sealer 26 exhibited the lowest levels of oxidative stress and IL‐1β and TNF‐α expression, regardless of the presence of LPS (p < .05).ConclusionsAlthough all sealers interfere with the response of macrophages to LPS, contact with epoxy resin‐based sealers can impair cell activity in vitro, while bioceramic sealer seems to favour the inflammatory functions of these cells.
Abstract Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS). Methodology After initial setting, the sealers were conditioned with serum‐free culture medium for 24 h (1 ml/cm 2 ). Macrophages from the RAW 264.7 strain were exposed to sealer extracts in a 1:16 ratio in a culture medium with or without LPS. Cell morphology, viability, mitochondrial activity, oxidative stress and gene expression of interleukin 1β (IL‐1β) and tumour necrosis factor‐alpha (TNF‐α) were evaluated. Data on mitochondrial activity, oxidative stress and TNF‐α were analysed using a two‐way analysis of variance ( anova ) test, followed by the Student–Newman–Keuls post‐test. IL‐1β data were analysed using one‐way anova , followed by SNK, and the t‐test was used for intragroup comparison. The significance level was set at 5%. Results In the absence of LPS, only AH Plus and Sealer 26 showed a reduction in cell density, while in the presence of LPS, Sealer 26 had the lowest density compared to the other groups. In terms of mitochondrial activity, at 24 and 48 h, Sealer Plus BC had significantly higher mean values than Sealer 26 and AH Plus ( p  < .05). Sealer 26 exhibited the lowest levels of oxidative stress and IL‐1β and TNF‐α expression, regardless of the presence of LPS ( p  < .05). Conclusions Although all sealers interfere with the response of macrophages to LPS, contact with epoxy resin‐based sealers can impair cell activity in vitro , while bioceramic sealer seems to favour the inflammatory functions of these cells.
To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS). After initial setting, the sealers were conditioned with serum-free culture medium for 24 h (1 ml/cm ). Macrophages from the RAW 264.7 strain were exposed to sealer extracts in a 1:16 ratio in a culture medium with or without LPS. Cell morphology, viability, mitochondrial activity, oxidative stress and gene expression of interleukin 1β (IL-1β) and tumour necrosis factor-alpha (TNF-α) were evaluated. Data on mitochondrial activity, oxidative stress and TNF-α were analysed using a two-way analysis of variance (anova) test, followed by the Student-Newman-Keuls post-test. IL-1β data were analysed using one-way anova, followed by SNK, and the t-test was used for intragroup comparison. The significance level was set at 5%. In the absence of LPS, only AH Plus and Sealer 26 showed a reduction in cell density, while in the presence of LPS, Sealer 26 had the lowest density compared to the other groups. In terms of mitochondrial activity, at 24 and 48 h, Sealer Plus BC had significantly higher mean values than Sealer 26 and AH Plus (p < .05). Sealer 26 exhibited the lowest levels of oxidative stress and IL-1β and TNF-α expression, regardless of the presence of LPS (p < .05). Although all sealers interfere with the response of macrophages to LPS, contact with epoxy resin-based sealers can impair cell activity in vitro, while bioceramic sealer seems to favour the inflammatory functions of these cells.
Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in macrophage cultures exposed to bacterial lipopolysaccharide (LPS). Methodology After initial setting, the sealers were conditioned with serum‐free culture medium for 24 h (1 ml/cm2). Macrophages from the RAW 264.7 strain were exposed to sealer extracts in a 1:16 ratio in a culture medium with or without LPS. Cell morphology, viability, mitochondrial activity, oxidative stress and gene expression of interleukin 1β (IL‐1β) and tumour necrosis factor‐alpha (TNF‐α) were evaluated. Data on mitochondrial activity, oxidative stress and TNF‐α were analysed using a two‐way analysis of variance (anova) test, followed by the Student–Newman–Keuls post‐test. IL‐1β data were analysed using one‐way anova, followed by SNK, and the t‐test was used for intragroup comparison. The significance level was set at 5%. Results In the absence of LPS, only AH Plus and Sealer 26 showed a reduction in cell density, while in the presence of LPS, Sealer 26 had the lowest density compared to the other groups. In terms of mitochondrial activity, at 24 and 48 h, Sealer Plus BC had significantly higher mean values than Sealer 26 and AH Plus (p < .05). Sealer 26 exhibited the lowest levels of oxidative stress and IL‐1β and TNF‐α expression, regardless of the presence of LPS (p < .05). Conclusions Although all sealers interfere with the response of macrophages to LPS, contact with epoxy resin‐based sealers can impair cell activity in vitro, while bioceramic sealer seems to favour the inflammatory functions of these cells.
Author Raucci Neto, Walter
Oliveira, Paulo Tambasco
Martorano, Antônio Secco
Messias, Nadyne Saab
Castro Raucci, Larissa Moreira Spinola
Bighetti‐Trevisan, Rayana Longo
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Snippet Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation...
To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation in...
Abstract Aim To evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and...
AimTo evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation...
AIMTo evaluate the effects of AH Plus (Dentsply), Sealer 26 (Dentsply), and Sealer Plus BC (Produtos Médicos e Odontológicos) on cytotoxicity and inflammation...
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pubmed
wiley
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StartPage 213
SubjectTerms biomaterials
Cell culture
Cell density
Cells, Cultured
Culture Media
Cytology
Cytotoxicity
Epoxy Resins
Gene expression
Humans
Inflammation
Lipopolysaccharides
Lipopolysaccharides - pharmacology
Macrophages
Materials Testing
Mitochondria
Oxidative stress
Root Canal Filling Materials - pharmacology
Sealing compounds
Silicates - pharmacology
Tumor necrosis factor
Tumor Necrosis Factor-alpha
Tumor necrosis factor-TNF
Tumors
Variance analysis
Title In vitro inflammatory modulation of bioceramic endodontic sealer in macrophages stimulated by bacterial lipopolysaccharide
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fiej.13858
https://www.ncbi.nlm.nih.gov/pubmed/36314853
https://www.proquest.com/docview/2764702867/abstract/
https://search.proquest.com/docview/2730647321
Volume 56
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