Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation

Detalhes bibliográficos
Autor(a) principal: Mendes Soares, Igor Paulino [UNESP]
Data de Publicação: 2022
Outros Autores: Anselmi, Caroline [UNESP], Guiné, Isabela [UNESP], Fernandes, Lídia de Oliveira [UNESP], Pires, Maria Luiza Barucci Araujo [UNESP], de Souza Costa, Carlos Alberto [UNESP], Scheffel, Débora Lopes Salles, Hebling, Josimeri [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.jdent.2022.104237
http://hdl.handle.net/11449/242084
Resumo: Objectives: To evaluate the inhibitory activity of an ion-releasing filler (S-PRG) eluate on dentin collagen-bound metalloproteinases (MMPs) and dentin matrix degradation. Methods: Dentin beams (5 × 2 × 0.5 mm) from human molars were completely demineralized to produce dentin matrix specimens. The dry mass was measured, and a colorimetric assay (Sensolyte) determined the initial total MMP activity to allocate the beams into four treatment groups (n = 10/group): 1) water for 1 min (negative control); 2) 2% chlorhexidine digluconate (CHX – inhibitor control) for 1 min; 3) S-PRG eluate for 1 min; 4) S-PRG eluate for 30 min. After the treatments, the total MMP activity was reassessed. The specimens were stored in simulated body fluid (SBF) at 37 °C for up to 21 days. The dry mass was reassessed weekly. On day 7, the dentin matrix degradation was analyzed for the presence of collagen fragments (CF; Sirius Red) and hydroxyproline (Hyp) in the SBF. Statistical analyses were performed with ANOVA/Tukey, paired t-tests, and RM-ANOVA/Sidak (α = 5%). Results: S-PRG eluate exposure for 1 and 30 min reduced (p < 0.0001) MMP activity. S-PRG exposure for 30 min presented MMP activity inhibition equivalent to CHX (p = 0.061). S-PRG and CHX decreased CF (p ≤ 0.007) and Hyp (p < 0.046) release. After 21 days of storage, S-PRG-treated beams, regardless of exposure time, presented a reduced (p ≤ 0.017) mass loss, intermediate between CHX and control. Conclusion: Treating demineralized dentin with S-PRG eluate for 1 or 30 min reduced matrix-bound MMP activity and dentin matrix degradation for up to 21 days. Clinical significance: S-PRG filler may hinder the progression of dentin carious/erosive lesions and enhance the stabilization of dentin bonding interfaces.
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spelling Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradationCollagenDentinHydroxyprolineMMPPre-reacted glass fillerProteolysisObjectives: To evaluate the inhibitory activity of an ion-releasing filler (S-PRG) eluate on dentin collagen-bound metalloproteinases (MMPs) and dentin matrix degradation. Methods: Dentin beams (5 × 2 × 0.5 mm) from human molars were completely demineralized to produce dentin matrix specimens. The dry mass was measured, and a colorimetric assay (Sensolyte) determined the initial total MMP activity to allocate the beams into four treatment groups (n = 10/group): 1) water for 1 min (negative control); 2) 2% chlorhexidine digluconate (CHX – inhibitor control) for 1 min; 3) S-PRG eluate for 1 min; 4) S-PRG eluate for 30 min. After the treatments, the total MMP activity was reassessed. The specimens were stored in simulated body fluid (SBF) at 37 °C for up to 21 days. The dry mass was reassessed weekly. On day 7, the dentin matrix degradation was analyzed for the presence of collagen fragments (CF; Sirius Red) and hydroxyproline (Hyp) in the SBF. Statistical analyses were performed with ANOVA/Tukey, paired t-tests, and RM-ANOVA/Sidak (α = 5%). Results: S-PRG eluate exposure for 1 and 30 min reduced (p < 0.0001) MMP activity. S-PRG exposure for 30 min presented MMP activity inhibition equivalent to CHX (p = 0.061). S-PRG and CHX decreased CF (p ≤ 0.007) and Hyp (p < 0.046) release. After 21 days of storage, S-PRG-treated beams, regardless of exposure time, presented a reduced (p ≤ 0.017) mass loss, intermediate between CHX and control. Conclusion: Treating demineralized dentin with S-PRG eluate for 1 or 30 min reduced matrix-bound MMP activity and dentin matrix degradation for up to 21 days. Clinical significance: S-PRG filler may hinder the progression of dentin carious/erosive lesions and enhance the stabilization of dentin bonding interfaces.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP)Department of Genetics Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP)Department of Restorative Dentistry School of Dentistry São Paulo State University (UNESP)Department of Physiology and Pathology School of Dentistry São Paulo State University (UNESP)Department of Dentistry Maringá State University (UEM), ParanáDepartment of Dental Materials and Prosthodontics School of Dentistry São Paulo State University (UNESP)Department of Genetics Morphology Orthodontics and Pediatric Dentistry School of Dentistry São Paulo State University (UNESP)Department of Restorative Dentistry School of Dentistry São Paulo State University (UNESP)Department of Physiology and Pathology School of Dentistry São Paulo State University (UNESP)CNPq: 138984/2020–4FAPESP: 2019/16473–1CNPq: 303391/2019–7Universidade Estadual Paulista (UNESP)Universidade Estadual de Maringá (UEM)Mendes Soares, Igor Paulino [UNESP]Anselmi, Caroline [UNESP]Guiné, Isabela [UNESP]Fernandes, Lídia de Oliveira [UNESP]Pires, Maria Luiza Barucci Araujo [UNESP]de Souza Costa, Carlos Alberto [UNESP]Scheffel, Débora Lopes SallesHebling, Josimeri [UNESP]2023-03-02T08:37:44Z2023-03-02T08:37:44Z2022-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.jdent.2022.104237Journal of Dentistry, v. 124.0300-5712http://hdl.handle.net/11449/24208410.1016/j.jdent.2022.1042372-s2.0-85134944888Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Dentistryinfo:eu-repo/semantics/openAccess2023-03-02T08:37:44Zoai:repositorio.unesp.br:11449/242084Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-03-02T08:37:44Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
title Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
spellingShingle Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
Mendes Soares, Igor Paulino [UNESP]
Collagen
Dentin
Hydroxyproline
MMP
Pre-reacted glass filler
Proteolysis
title_short Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
title_full Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
title_fullStr Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
title_full_unstemmed Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
title_sort Inhibitory activity of S-PRG filler on collagen-bound MMPs and dentin matrix degradation
author Mendes Soares, Igor Paulino [UNESP]
author_facet Mendes Soares, Igor Paulino [UNESP]
Anselmi, Caroline [UNESP]
Guiné, Isabela [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Pires, Maria Luiza Barucci Araujo [UNESP]
de Souza Costa, Carlos Alberto [UNESP]
Scheffel, Débora Lopes Salles
Hebling, Josimeri [UNESP]
author_role author
author2 Anselmi, Caroline [UNESP]
Guiné, Isabela [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Pires, Maria Luiza Barucci Araujo [UNESP]
de Souza Costa, Carlos Alberto [UNESP]
Scheffel, Débora Lopes Salles
Hebling, Josimeri [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade Estadual de Maringá (UEM)
dc.contributor.author.fl_str_mv Mendes Soares, Igor Paulino [UNESP]
Anselmi, Caroline [UNESP]
Guiné, Isabela [UNESP]
Fernandes, Lídia de Oliveira [UNESP]
Pires, Maria Luiza Barucci Araujo [UNESP]
de Souza Costa, Carlos Alberto [UNESP]
Scheffel, Débora Lopes Salles
Hebling, Josimeri [UNESP]
dc.subject.por.fl_str_mv Collagen
Dentin
Hydroxyproline
MMP
Pre-reacted glass filler
Proteolysis
topic Collagen
Dentin
Hydroxyproline
MMP
Pre-reacted glass filler
Proteolysis
description Objectives: To evaluate the inhibitory activity of an ion-releasing filler (S-PRG) eluate on dentin collagen-bound metalloproteinases (MMPs) and dentin matrix degradation. Methods: Dentin beams (5 × 2 × 0.5 mm) from human molars were completely demineralized to produce dentin matrix specimens. The dry mass was measured, and a colorimetric assay (Sensolyte) determined the initial total MMP activity to allocate the beams into four treatment groups (n = 10/group): 1) water for 1 min (negative control); 2) 2% chlorhexidine digluconate (CHX – inhibitor control) for 1 min; 3) S-PRG eluate for 1 min; 4) S-PRG eluate for 30 min. After the treatments, the total MMP activity was reassessed. The specimens were stored in simulated body fluid (SBF) at 37 °C for up to 21 days. The dry mass was reassessed weekly. On day 7, the dentin matrix degradation was analyzed for the presence of collagen fragments (CF; Sirius Red) and hydroxyproline (Hyp) in the SBF. Statistical analyses were performed with ANOVA/Tukey, paired t-tests, and RM-ANOVA/Sidak (α = 5%). Results: S-PRG eluate exposure for 1 and 30 min reduced (p < 0.0001) MMP activity. S-PRG exposure for 30 min presented MMP activity inhibition equivalent to CHX (p = 0.061). S-PRG and CHX decreased CF (p ≤ 0.007) and Hyp (p < 0.046) release. After 21 days of storage, S-PRG-treated beams, regardless of exposure time, presented a reduced (p ≤ 0.017) mass loss, intermediate between CHX and control. Conclusion: Treating demineralized dentin with S-PRG eluate for 1 or 30 min reduced matrix-bound MMP activity and dentin matrix degradation for up to 21 days. Clinical significance: S-PRG filler may hinder the progression of dentin carious/erosive lesions and enhance the stabilization of dentin bonding interfaces.
publishDate 2022
dc.date.none.fl_str_mv 2022-09-01
2023-03-02T08:37:44Z
2023-03-02T08:37:44Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jdent.2022.104237
Journal of Dentistry, v. 124.
0300-5712
http://hdl.handle.net/11449/242084
10.1016/j.jdent.2022.104237
2-s2.0-85134944888
url http://dx.doi.org/10.1016/j.jdent.2022.104237
http://hdl.handle.net/11449/242084
identifier_str_mv Journal of Dentistry, v. 124.
0300-5712
10.1016/j.jdent.2022.104237
2-s2.0-85134944888
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Dentistry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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