Bone remodeling during alveolar repair is impaired by RANKL antagonist

Detalhes bibliográficos
Autor(a) principal: Silva, Ana Cláudia Ervolino da
Data de Publicação: 2021
Outros Autores: Batista, Fábio Roberto de Souza, Moura, Juliana de, Coléte, Juliana Zorzi, Chiba, Fernando, Gomes-Ferreira, Pedro Henrique Silva, Okamoto, Roberta
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/11975
Resumo: Post-menopausal osteoporosis is detrimental to bone metabolism as well as alveolar repair. This osteometabolic disorder is an obstacle to the success of maxillofacial rehabilitations, since a large number of patients are carriers of the disease. Denosumab is widely used as a treatment for post menopausal osteoporosis. This drug exerts an antiabsorptive action by inhibiting RANKL, helping to reduce the bone loss caused by osteoporosis.  This study aimed to evaluate the repair bone formed after the extraction of the upper incisor of estrogen-deficient rats treated with anti-RANKL monoclonal antibody. The rats (Rattus novergicus albinus, Wistar) were ovariectomized or SHAM operated (n=36). Half of the ovariectomized rats were treated with osteoprotegerin with an Fc fragment (OPG-Fc; 10mg/kg, twice a week), the other half received saline solution as control. After 30 days the rats had their right upper incisor extracted. After 60 days of extraction, the alveoli were evaluated by immunohistochemical, computerized microtomography and confocal microscopy. The OPG-Fc decreased the percentage of bone volume (BV/TV), thickness (Tb.Th) and number of alveolar trabecules (Tb.N) when compared to groups that received saline solution (p<0.005). The OPG-Fc increased the separation between the trabecules (Tb.Sp) and the porosity (Po.tot) of the reparative alveolar bone (p<0.005). The OPG-Fc decreased immunolabelling for RANKL and TRAP when compared to groups that received saline solution. Treatment with OPG-Fc decreased bone neoformation but preserved preexisting bone tissue. This data is supported by the mineral apposition rate, which showed higher values for OVX/OPG-Fc when compared to the OVX group.
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spelling Bone remodeling during alveolar repair is impaired by RANKL antagonistLa remodelación ósea durante la reparación alveolar se ve afectada por el antagonista de RANKLRemodelação óssea durante o reparo alveolar é prejudicada por antagonista da RANKLOsteoporoseRemodelação ósseaDensidade ósseaAlvéolo dentalDenosumab.OsteoporosisRemodelación óseaDensidad oseaAlvéolo dentalDenosumab.OsteoporosisBone remodelingBone densityTooth socketDenosumab.Post-menopausal osteoporosis is detrimental to bone metabolism as well as alveolar repair. This osteometabolic disorder is an obstacle to the success of maxillofacial rehabilitations, since a large number of patients are carriers of the disease. Denosumab is widely used as a treatment for post menopausal osteoporosis. This drug exerts an antiabsorptive action by inhibiting RANKL, helping to reduce the bone loss caused by osteoporosis.  This study aimed to evaluate the repair bone formed after the extraction of the upper incisor of estrogen-deficient rats treated with anti-RANKL monoclonal antibody. The rats (Rattus novergicus albinus, Wistar) were ovariectomized or SHAM operated (n=36). Half of the ovariectomized rats were treated with osteoprotegerin with an Fc fragment (OPG-Fc; 10mg/kg, twice a week), the other half received saline solution as control. After 30 days the rats had their right upper incisor extracted. After 60 days of extraction, the alveoli were evaluated by immunohistochemical, computerized microtomography and confocal microscopy. The OPG-Fc decreased the percentage of bone volume (BV/TV), thickness (Tb.Th) and number of alveolar trabecules (Tb.N) when compared to groups that received saline solution (p<0.005). The OPG-Fc increased the separation between the trabecules (Tb.Sp) and the porosity (Po.tot) of the reparative alveolar bone (p<0.005). The OPG-Fc decreased immunolabelling for RANKL and TRAP when compared to groups that received saline solution. Treatment with OPG-Fc decreased bone neoformation but preserved preexisting bone tissue. This data is supported by the mineral apposition rate, which showed higher values for OVX/OPG-Fc when compared to the OVX group.La osteoporosis posmenopáusica es perjudicial para el metabolismo óseo y la reparación alveolar. Este trastorno osteometabólico es un obstáculo para el éxito de las rehabilitaciones maxilofaciales, ya que un gran número de pacientes son portadores de la enfermedad. El denosumab se usa ampliamente como tratamiento para la osteoporosis posmenopáusica. Este fármaco ejerce una acción antiabsorbente al inhibir RANKL, ayudando a reducir la pérdida ósea provocada por la osteoporosis. Este estudio tuvo como objetivo evaluar el hueso de reparación formado tras la extracción del incisivo superior de ratas deficientes en estrógenos tratadas con anticuerpo monoclonal anti-RANKL. Las ratas (Rattus novergicus albinus, Wistar) fueron ovariectomizadas u operadas con SHAM (n = 36). La mitad de las ratas ovariectomizadas fueron tratadas con osteoprotegerina con un fragmento Fc (OPG-Fc; 10 mg / kg, dos veces por semana), la otra mitad recibió solución salina como control. Después de 30 días, se extrajo el incisivo superior derecho de las ratas. Después de 60 días de extracción, los alvéolos fueron evaluados por inmunohistoquímica, microtomografía computarizada y microscopía confocal. La OPG-Fc disminuyó el porcentaje de volumen óseo (BV / TV), grosor (Tb.Th) y número de trabéculas alveolares (Tb.N) en comparación con los grupos que recibieron solución salina (p <0,005). La OPG-Fc aumentó la separación entre las trabéculas (Tb.Sp) y la porosidad (Po.tot) del hueso alveolar reparador (p <0,005). El OPG-Fc disminuyó el inmunomarcaje de RANKL y TRAP en comparación con los grupos que recibieron solución salina. El tratamiento con OPG-Fc disminuyó la neoformación ósea pero conservó el tejido óseo preexistente. Estos datos están respaldados por la tasa de aposición de minerales, que mostró valores más altos para OVX / OPG-Fc en comparación con el grupo OVX.A osteoporose pós menopáusica é prejudicial ao metabolismo ósseo, bem como ao reparo alveolar. Essa desordem osteometabólica é um obstáculo para o sucesso das reabilitações maxilofaciais, visto que uma grande parcela dos pacientes são portadores da doença. O Denosumab é amplamente utilizado como tratamento da osteoporose pós menopáusica. Esse medicamento exerce ação antireabsortiva pela inibição do RANKL, auxiliando na diminuição da perda óssea provocada pela osteoporose.  Este estudo teve como objetivo a avaliação do osso reparacional formado após a exodontia do incisivo superior de ratas com deficiência de estrógeno tratadas com o anticorpo monoclonal anti-RANKL. As ratas (Rattus novergicus albinus, Wistar) foram ovariectomizadas ou SHAM operadas (n=36). Metade das ratas ovariectomizadas receberam tratamento com osteoprotegerina com um fragmento Fc (OPG-Fc; 10mg/kg, duas vezes por semana), o restante das ratas recebeu solução salina como controle. Após 30 dias as ratas tiveram o incisivo superior direito extraído. Decorridos 60 dias da exodontia, os alvéolos foram avaliados por imunoistoquímica, microtomografia computadorizada e microscopia confocal. A OPG-Fc diminuiu a porcentagem de volume ósseo (BV/TV), espessura (Tb.Th) o número das trabéculas (Tb.N) alveolares quando em comparação aos grupos que receberam solução salina (p<0,005). A OPG-Fc aumentou a separação entre as trabéculas (Tb.Sp) e a porosidade (Po.tot) do osso alveolar reparacional (p<0,005). A OPG-Fc diminuiu a imunomarcação para RANKL e TRAP quando comparada aos grupos que receberam solução salina. O tratamento com OPG-Fc diminuiu a neoformação óssea, mas preservou o tecido ósseo preexistente. Esse dado é suportado pela taxa de aposição mineral, que apresentou valores maiores para OVX/OPG-Fc quando comparado ao grupo OVX.Research, Society and Development2021-01-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/1197510.33448/rsd-v10i1.11975Research, Society and Development; Vol. 10 No. 1; e43710111975Research, Society and Development; Vol. 10 Núm. 1; e43710111975Research, Society and Development; v. 10 n. 1; e437101119752525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/11975/10762Copyright (c) 2021 Ana Cláudia Ervolino da Silva; Fábio Roberto de Souza Batista; Juliana de Moura; Juliana Zorzi Coléte; Fernando Chiba; Pedro Henrique Silva Gomes-Ferreira; Roberta Okamotohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSilva, Ana Cláudia Ervolino da Batista, Fábio Roberto de Souza Moura, Juliana de Coléte, Juliana Zorzi Chiba, Fernando Gomes-Ferreira, Pedro Henrique Silva Okamoto, Roberta 2021-02-20T21:19:23Zoai:ojs.pkp.sfu.ca:article/11975Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:33:40.257415Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Bone remodeling during alveolar repair is impaired by RANKL antagonist
La remodelación ósea durante la reparación alveolar se ve afectada por el antagonista de RANKL
Remodelação óssea durante o reparo alveolar é prejudicada por antagonista da RANKL
title Bone remodeling during alveolar repair is impaired by RANKL antagonist
spellingShingle Bone remodeling during alveolar repair is impaired by RANKL antagonist
Silva, Ana Cláudia Ervolino da
Osteoporose
Remodelação óssea
Densidade óssea
Alvéolo dental
Denosumab.
Osteoporosis
Remodelación ósea
Densidad osea
Alvéolo dental
Denosumab.
Osteoporosis
Bone remodeling
Bone density
Tooth socket
Denosumab.
title_short Bone remodeling during alveolar repair is impaired by RANKL antagonist
title_full Bone remodeling during alveolar repair is impaired by RANKL antagonist
title_fullStr Bone remodeling during alveolar repair is impaired by RANKL antagonist
title_full_unstemmed Bone remodeling during alveolar repair is impaired by RANKL antagonist
title_sort Bone remodeling during alveolar repair is impaired by RANKL antagonist
author Silva, Ana Cláudia Ervolino da
author_facet Silva, Ana Cláudia Ervolino da
Batista, Fábio Roberto de Souza
Moura, Juliana de
Coléte, Juliana Zorzi
Chiba, Fernando
Gomes-Ferreira, Pedro Henrique Silva
Okamoto, Roberta
author_role author
author2 Batista, Fábio Roberto de Souza
Moura, Juliana de
Coléte, Juliana Zorzi
Chiba, Fernando
Gomes-Ferreira, Pedro Henrique Silva
Okamoto, Roberta
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, Ana Cláudia Ervolino da
Batista, Fábio Roberto de Souza
Moura, Juliana de
Coléte, Juliana Zorzi
Chiba, Fernando
Gomes-Ferreira, Pedro Henrique Silva
Okamoto, Roberta
dc.subject.por.fl_str_mv Osteoporose
Remodelação óssea
Densidade óssea
Alvéolo dental
Denosumab.
Osteoporosis
Remodelación ósea
Densidad osea
Alvéolo dental
Denosumab.
Osteoporosis
Bone remodeling
Bone density
Tooth socket
Denosumab.
topic Osteoporose
Remodelação óssea
Densidade óssea
Alvéolo dental
Denosumab.
Osteoporosis
Remodelación ósea
Densidad osea
Alvéolo dental
Denosumab.
Osteoporosis
Bone remodeling
Bone density
Tooth socket
Denosumab.
description Post-menopausal osteoporosis is detrimental to bone metabolism as well as alveolar repair. This osteometabolic disorder is an obstacle to the success of maxillofacial rehabilitations, since a large number of patients are carriers of the disease. Denosumab is widely used as a treatment for post menopausal osteoporosis. This drug exerts an antiabsorptive action by inhibiting RANKL, helping to reduce the bone loss caused by osteoporosis.  This study aimed to evaluate the repair bone formed after the extraction of the upper incisor of estrogen-deficient rats treated with anti-RANKL monoclonal antibody. The rats (Rattus novergicus albinus, Wistar) were ovariectomized or SHAM operated (n=36). Half of the ovariectomized rats were treated with osteoprotegerin with an Fc fragment (OPG-Fc; 10mg/kg, twice a week), the other half received saline solution as control. After 30 days the rats had their right upper incisor extracted. After 60 days of extraction, the alveoli were evaluated by immunohistochemical, computerized microtomography and confocal microscopy. The OPG-Fc decreased the percentage of bone volume (BV/TV), thickness (Tb.Th) and number of alveolar trabecules (Tb.N) when compared to groups that received saline solution (p<0.005). The OPG-Fc increased the separation between the trabecules (Tb.Sp) and the porosity (Po.tot) of the reparative alveolar bone (p<0.005). The OPG-Fc decreased immunolabelling for RANKL and TRAP when compared to groups that received saline solution. Treatment with OPG-Fc decreased bone neoformation but preserved preexisting bone tissue. This data is supported by the mineral apposition rate, which showed higher values for OVX/OPG-Fc when compared to the OVX group.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-24
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/11975
10.33448/rsd-v10i1.11975
url https://rsdjournal.org/index.php/rsd/article/view/11975
identifier_str_mv 10.33448/rsd-v10i1.11975
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/11975/10762
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 10 No. 1; e43710111975
Research, Society and Development; Vol. 10 Núm. 1; e43710111975
Research, Society and Development; v. 10 n. 1; e43710111975
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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