DBBM shows no signs of resorption under inflammatory conditions. An experimental study in the mouse calvaria
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1813546480902864896 |