DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria

Detalhes bibliográficos
Autor(a) principal: Kuchler, Ulrike
Data de Publicação: 2019
Outros Autores: Santos, Gabriel Mulinari dos [UNESP], Heimel, Patrick, Staehli, Alexandra, Strauss, Franz Josef, Tangl, Stefan, Gruber, Reinhard
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1111/clr.13538
http://hdl.handle.net/11449/196221
Resumo: Objectives Deproteinized bovine bone mineral (DBBM) is not resorbable. However, the behavior of DBBM under inflammatory conditions remains unclear. Aim of the study was therefore to evaluate the resorption of DBBM under local inflammatory conditions in vivo using the calvarial osteolysis model. Methods In thirty adult BALB/c mice, DBBM was implanted into the space between the elevated soft tissue and the calvarial bone. Inflammation was induced either by lipopolysaccharides (LPS) injection or by polyethylene particles (Ceridust) mixed with DBBM. Three modalities were randomly applied (n = 10 each): (a) DBBM alone (control), (b) DBBM + LPS, and (c) DBBM + polyethylene particles (Ceridust). Mice were euthanized on day fourteen, and each calvarium was subjected to histological and mu CT analysis. Primary outcome was the size distribution of the DBBM particles. Secondary outcome was the surface erosion of the calvarial bone. Results Histological and mu CT analysis revealed that the size distribution and the volume of DBBM particles in the augmented site were similar between DBBM alone and the combinations with LPS or polyethylene particles. Moreover, histological evaluation showed no signs of erosions of DBBM particles under inflammatory conditions. mu CT analysis and histology further revealed that LPS and the polyethylene particles, but not the DBBM alone, caused severe erosions of the calvarial bone as indicated by large voids representing the massive compensatory new immature woven bone formation on the endosteal surface. Conclusions Local calvarial bone but not the DBBM particles undergo severe resorption and subsequent new bone formation under inflammatory conditions in a mouse model.
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spelling DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvariabone regenerationbone substitutescalvariainflammationmiceosteoclastsObjectives Deproteinized bovine bone mineral (DBBM) is not resorbable. However, the behavior of DBBM under inflammatory conditions remains unclear. Aim of the study was therefore to evaluate the resorption of DBBM under local inflammatory conditions in vivo using the calvarial osteolysis model. Methods In thirty adult BALB/c mice, DBBM was implanted into the space between the elevated soft tissue and the calvarial bone. Inflammation was induced either by lipopolysaccharides (LPS) injection or by polyethylene particles (Ceridust) mixed with DBBM. Three modalities were randomly applied (n = 10 each): (a) DBBM alone (control), (b) DBBM + LPS, and (c) DBBM + polyethylene particles (Ceridust). Mice were euthanized on day fourteen, and each calvarium was subjected to histological and mu CT analysis. Primary outcome was the size distribution of the DBBM particles. Secondary outcome was the surface erosion of the calvarial bone. Results Histological and mu CT analysis revealed that the size distribution and the volume of DBBM particles in the augmented site were similar between DBBM alone and the combinations with LPS or polyethylene particles. Moreover, histological evaluation showed no signs of erosions of DBBM particles under inflammatory conditions. mu CT analysis and histology further revealed that LPS and the polyethylene particles, but not the DBBM alone, caused severe erosions of the calvarial bone as indicated by large voids representing the massive compensatory new immature woven bone formation on the endosteal surface. Conclusions Local calvarial bone but not the DBBM particles undergo severe resorption and subsequent new bone formation under inflammatory conditions in a mouse model.Osteology FoundationAustrian Science FundMed Univ Vienna, Univ Clin Dent, Dept Oral Surg, Vienna, AustriaUniv Estadual Paulista, Aracatuba Dent Sch, Dept Oral Surg, Aracatuba, BrazilUniv Estadual Paulista, Aracatuba Dent Sch, Integrated Clin, Aracatuba, BrazilMed Univ Vienna, Univ Clin Dent, Karl Donath Lab, Core Facil Hard Tissue & Biomat Res, Vienna, AustriaMed Univ Vienna, Univ Clin Dent, Dept Oral Biol, Vienna, AustriaLudwig Boltzmann Inst Clin & Expt Traumatol, Vienna, AustriaAustrian Cluster Tissue Regenerat, Vienna, AustriaUniv Bern, Sch Dent Med, Dept Periodontol, Bern, SwitzerlandUniv Chile, Sch Dent, Dept Conservat Dent, Santiago, ChileUniv Estadual Paulista, Aracatuba Dent Sch, Dept Oral Surg, Aracatuba, BrazilUniv Estadual Paulista, Aracatuba Dent Sch, Integrated Clin, Aracatuba, BrazilOsteology Foundation: 14-126Austrian Science Fund: 4072-B28Wiley-BlackwellMed Univ ViennaUniversidade Estadual Paulista (Unesp)Ludwig Boltzmann Inst Clin & Expt TraumatolAustrian Cluster Tissue RegeneratUniv BernUniv ChileKuchler, UlrikeSantos, Gabriel Mulinari dos [UNESP]Heimel, PatrickStaehli, AlexandraStrauss, Franz JosefTangl, StefanGruber, Reinhard2020-12-10T19:37:36Z2020-12-10T19:37:36Z2019-09-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10-17http://dx.doi.org/10.1111/clr.13538Clinical Oral Implants Research. Hoboken: Wiley, v. 31, n. 1, p. 10-17, 2020.0905-7161http://hdl.handle.net/11449/19622110.1111/clr.13538WOS:000488579900001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical Oral Implants Researchinfo:eu-repo/semantics/openAccess2024-09-19T13:30:44Zoai:repositorio.unesp.br:11449/196221Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T13:30:44Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
title DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
spellingShingle DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
Kuchler, Ulrike
bone regeneration
bone substitutes
calvaria
inflammation
mice
osteoclasts
title_short DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
title_full DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
title_fullStr DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
title_full_unstemmed DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
title_sort DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
author Kuchler, Ulrike
author_facet Kuchler, Ulrike
Santos, Gabriel Mulinari dos [UNESP]
Heimel, Patrick
Staehli, Alexandra
Strauss, Franz Josef
Tangl, Stefan
Gruber, Reinhard
author_role author
author2 Santos, Gabriel Mulinari dos [UNESP]
Heimel, Patrick
Staehli, Alexandra
Strauss, Franz Josef
Tangl, Stefan
Gruber, Reinhard
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Med Univ Vienna
Universidade Estadual Paulista (Unesp)
Ludwig Boltzmann Inst Clin & Expt Traumatol
Austrian Cluster Tissue Regenerat
Univ Bern
Univ Chile
dc.contributor.author.fl_str_mv Kuchler, Ulrike
Santos, Gabriel Mulinari dos [UNESP]
Heimel, Patrick
Staehli, Alexandra
Strauss, Franz Josef
Tangl, Stefan
Gruber, Reinhard
dc.subject.por.fl_str_mv bone regeneration
bone substitutes
calvaria
inflammation
mice
osteoclasts
topic bone regeneration
bone substitutes
calvaria
inflammation
mice
osteoclasts
description Objectives Deproteinized bovine bone mineral (DBBM) is not resorbable. However, the behavior of DBBM under inflammatory conditions remains unclear. Aim of the study was therefore to evaluate the resorption of DBBM under local inflammatory conditions in vivo using the calvarial osteolysis model. Methods In thirty adult BALB/c mice, DBBM was implanted into the space between the elevated soft tissue and the calvarial bone. Inflammation was induced either by lipopolysaccharides (LPS) injection or by polyethylene particles (Ceridust) mixed with DBBM. Three modalities were randomly applied (n = 10 each): (a) DBBM alone (control), (b) DBBM + LPS, and (c) DBBM + polyethylene particles (Ceridust). Mice were euthanized on day fourteen, and each calvarium was subjected to histological and mu CT analysis. Primary outcome was the size distribution of the DBBM particles. Secondary outcome was the surface erosion of the calvarial bone. Results Histological and mu CT analysis revealed that the size distribution and the volume of DBBM particles in the augmented site were similar between DBBM alone and the combinations with LPS or polyethylene particles. Moreover, histological evaluation showed no signs of erosions of DBBM particles under inflammatory conditions. mu CT analysis and histology further revealed that LPS and the polyethylene particles, but not the DBBM alone, caused severe erosions of the calvarial bone as indicated by large voids representing the massive compensatory new immature woven bone formation on the endosteal surface. Conclusions Local calvarial bone but not the DBBM particles undergo severe resorption and subsequent new bone formation under inflammatory conditions in a mouse model.
publishDate 2019
dc.date.none.fl_str_mv 2019-09-30
2020-12-10T19:37:36Z
2020-12-10T19:37:36Z
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/10.1111/clr.13538
Clinical Oral Implants Research. Hoboken: Wiley, v. 31, n. 1, p. 10-17, 2020.
0905-7161
http://hdl.handle.net/11449/196221
10.1111/clr.13538
WOS:000488579900001
url http://dx.doi.org/10.1111/clr.13538
http://hdl.handle.net/11449/196221
identifier_str_mv Clinical Oral Implants Research. Hoboken: Wiley, v. 31, n. 1, p. 10-17, 2020.
0905-7161
10.1111/clr.13538
WOS:000488579900001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical Oral Implants Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 10-17
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv Web of Science
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 repositoriounesp@unesp.br
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