Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats

Detalhes bibliográficos
Autor(a) principal: KÃtia do Nascimento Gomes
Data de Publicação: 2015
Tipo de documento: Tese
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UFC
Texto Completo: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591
Resumo: The alveolar bone repair model, through dental excision in rats, allows the longitudinal study of local and systemic parameters. This allows learning the pathophysiology in inflammatory bone remodeling process. The objective of the research was to investigate the effect of doxycycline associated or not with dexamethasone on the events that follow the bone reabsorption process in alveolar bone repair in rats. The animals (190-200 g) were treated daily (per os) with saline solution Control (SSC), doxycycline (DOX 10 and 25 mg/kg), Dexamethasone (DEXA 1 mg/kg) (IP), and sacrificed according to experimental group (7, 14 and 21 days) to remove their jaws, which were used in the qualitative analysis of microstructural parameters, histomorphometry, and immunohistochemistry for Wnt10b and Dkk-1. It was observed that DOX (10 and 25 mg / kg ) improve some parameters such as the number of osteoblasts increase, reduction in the number of osteoblasts and % increase in bone tissue compared to the CTL group. The results also showed an increase in the expression of Wnt 10b, and Dkk-1 reduction, during the process of bone repair in animals that received DOX (10 and 25 mg/kg), compared to groups CTL. These findings suggest that DOX offers osteoinductive and osteoprotector effects on bone tissue during the alveolar bone remodeling process. It is possible that, in addition to anti-inflammatory effects recognized in DOX, this Tetracycline can influence the expression of Wnt 10b, favoring bone neoformation, and modulate the expression of Dkk-1, inhibiting tissue resorption in the alveolus of the animals.
id UFC_b1e91dee6ebcc99fbd4b8690cdd54534
oai_identifier_str oai:www.teses.ufc.br:11400
network_acronym_str UFC
network_name_str Biblioteca Digital de Teses e Dissertações da UFC
spelling info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisAssessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in ratsAvaliaÃÃo do efeito da Doxiciclina associada ou nÃo à decametasone no modelo de reparo Ãsseo alveolar em ratos2015-11-27Glauce Socorro de Barros Viana00101761368http://lattes.cnpq.br/5043495454602083Ana Paula Negreiros Nunes Alves19242662372http://lattes.cnpq.br/5522921433940881 Paula Goes Pinheiro Dutra99298376391http://lattes.cnpq.br/9146660561423508Karuza Maria Alves Pereira78033977353http://lattes.cnpq.br/3193698890688967Fernando Andrà Campos Viana43384137353http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4778691H547716100378http://lattes.cnpq.br/8185407617152089KÃtia do Nascimento GomesUniversidade Federal do CearÃPrograma de PÃs-GraduaÃÃo em FarmacologiaUFCBRFARMACOLOGIAThe alveolar bone repair model, through dental excision in rats, allows the longitudinal study of local and systemic parameters. This allows learning the pathophysiology in inflammatory bone remodeling process. The objective of the research was to investigate the effect of doxycycline associated or not with dexamethasone on the events that follow the bone reabsorption process in alveolar bone repair in rats. The animals (190-200 g) were treated daily (per os) with saline solution Control (SSC), doxycycline (DOX 10 and 25 mg/kg), Dexamethasone (DEXA 1 mg/kg) (IP), and sacrificed according to experimental group (7, 14 and 21 days) to remove their jaws, which were used in the qualitative analysis of microstructural parameters, histomorphometry, and immunohistochemistry for Wnt10b and Dkk-1. It was observed that DOX (10 and 25 mg / kg ) improve some parameters such as the number of osteoblasts increase, reduction in the number of osteoblasts and % increase in bone tissue compared to the CTL group. The results also showed an increase in the expression of Wnt 10b, and Dkk-1 reduction, during the process of bone repair in animals that received DOX (10 and 25 mg/kg), compared to groups CTL. These findings suggest that DOX offers osteoinductive and osteoprotector effects on bone tissue during the alveolar bone remodeling process. It is possible that, in addition to anti-inflammatory effects recognized in DOX, this Tetracycline can influence the expression of Wnt 10b, favoring bone neoformation, and modulate the expression of Dkk-1, inhibiting tissue resorption in the alveolus of the animals.O modelo de reparo Ãsseo alveolar atravÃs de exÃrese dentÃria em ratos permite que parÃmetros locais e sistÃmicos possam ser estudados longitudinalmente possibilitando o conhecimento da fisiopatogÃnese no processo de reabsorÃÃo Ãssea inflamatÃria. O objetivo da pesquisa foi investigar o efeito de doxiciclina associada ou nÃo à dexametasona sobre os eventos que sucedem o processo de remodelamento Ãsseo em modelo de reparo Ãsseo alveolar em ratos. Os animais (190-200 g) foram tratados diariamente (v.o.) com soluÃÃo salina Controle (CTL), doxiciclina (DOX 10mg/kg e 25 mg/kg), Dexametasona (DEXA 1 mg/kg)(i.p.) e sacrificados de acordo com grupo experimental (7, 14 e 21 dias) para remoÃÃo de suas maxilas utilizadas na anÃlise qualitativa de parÃmetros microestruturais, histomorfometria e imunohistoquÃmica para Wnt 10b e Dkk-1. Foi observado que DOX (10 e 25 mg/kg) melhoram alguns parÃmetros como: aumento do nÃmero de osteoblastos, reduÃÃo no nÃmero de osteoblastos e % de tecido Ãsseo comparados ao grupo CTL. Os resultados tambÃm mostraram um aumento na expressÃo de WNT 10b e reduÃÃo de Dkk-1 durante o processo de reparo Ãsseo nos animais que receberam DOX (10 e 25 mg/kg) quando comparados aos grupos CTL. Esses achados sugerem que DOX oferece um efeitos osteoindutor e osteoprotetor do tecido Ãsseo durante o processo de remodelamento Ãsseo alveolar. à possÃvel que alÃm dos efeitos antiiflamatÃrios reconhecidos em DOX, essa Tetraciclina pode influenciar a expressÃo de WNT 10b, favorecendo a neoformaÃÃo Ãssea ou modular a expressÃo de Dkk-1, inibindo a reabsorÃÃo tecidual nos alvÃolo dos animais.Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgicohttp://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591application/pdfinfo:eu-repo/semantics/openAccessporreponame:Biblioteca Digital de Teses e Dissertações da UFCinstname:Universidade Federal do Cearáinstacron:UFC2019-01-21T11:31:00Zmail@mail.com -
dc.title.en.fl_str_mv Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
dc.title.alternative.pt.fl_str_mv AvaliaÃÃo do efeito da Doxiciclina associada ou nÃo à decametasone no modelo de reparo Ãsseo alveolar em ratos
title Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
spellingShingle Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
KÃtia do Nascimento Gomes
FARMACOLOGIA
title_short Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
title_full Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
title_fullStr Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
title_full_unstemmed Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
title_sort Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
author KÃtia do Nascimento Gomes
author_facet KÃtia do Nascimento Gomes
author_role author
dc.contributor.advisor1.fl_str_mv Glauce Socorro de Barros Viana
dc.contributor.advisor1ID.fl_str_mv 00101761368
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/5043495454602083
dc.contributor.referee1.fl_str_mv Ana Paula Negreiros Nunes Alves
dc.contributor.referee1ID.fl_str_mv 19242662372
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/5522921433940881
dc.contributor.referee2.fl_str_mv Paula Goes Pinheiro Dutra
dc.contributor.referee2ID.fl_str_mv 99298376391
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/9146660561423508
dc.contributor.referee3.fl_str_mv Karuza Maria Alves Pereira
dc.contributor.referee3ID.fl_str_mv 78033977353
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/3193698890688967
dc.contributor.referee4.fl_str_mv Fernando Andrà Campos Viana
dc.contributor.referee4ID.fl_str_mv 43384137353
dc.contributor.referee4Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4778691H5
dc.contributor.authorID.fl_str_mv 47716100378
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/8185407617152089
dc.contributor.author.fl_str_mv KÃtia do Nascimento Gomes
contributor_str_mv Glauce Socorro de Barros Viana
Ana Paula Negreiros Nunes Alves
Paula Goes Pinheiro Dutra
Karuza Maria Alves Pereira
Fernando Andrà Campos Viana
dc.subject.cnpq.fl_str_mv FARMACOLOGIA
topic FARMACOLOGIA
dc.description.sponsorship.fl_txt_mv Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico
dc.description.abstract.por.fl_txt_mv The alveolar bone repair model, through dental excision in rats, allows the longitudinal study of local and systemic parameters. This allows learning the pathophysiology in inflammatory bone remodeling process. The objective of the research was to investigate the effect of doxycycline associated or not with dexamethasone on the events that follow the bone reabsorption process in alveolar bone repair in rats. The animals (190-200 g) were treated daily (per os) with saline solution Control (SSC), doxycycline (DOX 10 and 25 mg/kg), Dexamethasone (DEXA 1 mg/kg) (IP), and sacrificed according to experimental group (7, 14 and 21 days) to remove their jaws, which were used in the qualitative analysis of microstructural parameters, histomorphometry, and immunohistochemistry for Wnt10b and Dkk-1. It was observed that DOX (10 and 25 mg / kg ) improve some parameters such as the number of osteoblasts increase, reduction in the number of osteoblasts and % increase in bone tissue compared to the CTL group. The results also showed an increase in the expression of Wnt 10b, and Dkk-1 reduction, during the process of bone repair in animals that received DOX (10 and 25 mg/kg), compared to groups CTL. These findings suggest that DOX offers osteoinductive and osteoprotector effects on bone tissue during the alveolar bone remodeling process. It is possible that, in addition to anti-inflammatory effects recognized in DOX, this Tetracycline can influence the expression of Wnt 10b, favoring bone neoformation, and modulate the expression of Dkk-1, inhibiting tissue resorption in the alveolus of the animals.
O modelo de reparo Ãsseo alveolar atravÃs de exÃrese dentÃria em ratos permite que parÃmetros locais e sistÃmicos possam ser estudados longitudinalmente possibilitando o conhecimento da fisiopatogÃnese no processo de reabsorÃÃo Ãssea inflamatÃria. O objetivo da pesquisa foi investigar o efeito de doxiciclina associada ou nÃo à dexametasona sobre os eventos que sucedem o processo de remodelamento Ãsseo em modelo de reparo Ãsseo alveolar em ratos. Os animais (190-200 g) foram tratados diariamente (v.o.) com soluÃÃo salina Controle (CTL), doxiciclina (DOX 10mg/kg e 25 mg/kg), Dexametasona (DEXA 1 mg/kg)(i.p.) e sacrificados de acordo com grupo experimental (7, 14 e 21 dias) para remoÃÃo de suas maxilas utilizadas na anÃlise qualitativa de parÃmetros microestruturais, histomorfometria e imunohistoquÃmica para Wnt 10b e Dkk-1. Foi observado que DOX (10 e 25 mg/kg) melhoram alguns parÃmetros como: aumento do nÃmero de osteoblastos, reduÃÃo no nÃmero de osteoblastos e % de tecido Ãsseo comparados ao grupo CTL. Os resultados tambÃm mostraram um aumento na expressÃo de WNT 10b e reduÃÃo de Dkk-1 durante o processo de reparo Ãsseo nos animais que receberam DOX (10 e 25 mg/kg) quando comparados aos grupos CTL. Esses achados sugerem que DOX oferece um efeitos osteoindutor e osteoprotetor do tecido Ãsseo durante o processo de remodelamento Ãsseo alveolar. à possÃvel que alÃm dos efeitos antiiflamatÃrios reconhecidos em DOX, essa Tetraciclina pode influenciar a expressÃo de WNT 10b, favorecendo a neoformaÃÃo Ãssea ou modular a expressÃo de Dkk-1, inibindo a reabsorÃÃo tecidual nos alvÃolo dos animais.
description The alveolar bone repair model, through dental excision in rats, allows the longitudinal study of local and systemic parameters. This allows learning the pathophysiology in inflammatory bone remodeling process. The objective of the research was to investigate the effect of doxycycline associated or not with dexamethasone on the events that follow the bone reabsorption process in alveolar bone repair in rats. The animals (190-200 g) were treated daily (per os) with saline solution Control (SSC), doxycycline (DOX 10 and 25 mg/kg), Dexamethasone (DEXA 1 mg/kg) (IP), and sacrificed according to experimental group (7, 14 and 21 days) to remove their jaws, which were used in the qualitative analysis of microstructural parameters, histomorphometry, and immunohistochemistry for Wnt10b and Dkk-1. It was observed that DOX (10 and 25 mg / kg ) improve some parameters such as the number of osteoblasts increase, reduction in the number of osteoblasts and % increase in bone tissue compared to the CTL group. The results also showed an increase in the expression of Wnt 10b, and Dkk-1 reduction, during the process of bone repair in animals that received DOX (10 and 25 mg/kg), compared to groups CTL. These findings suggest that DOX offers osteoinductive and osteoprotector effects on bone tissue during the alveolar bone remodeling process. It is possible that, in addition to anti-inflammatory effects recognized in DOX, this Tetracycline can influence the expression of Wnt 10b, favoring bone neoformation, and modulate the expression of Dkk-1, inhibiting tissue resorption in the alveolus of the animals.
publishDate 2015
dc.date.issued.fl_str_mv 2015-11-27
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
status_str publishedVersion
format doctoralThesis
dc.identifier.uri.fl_str_mv http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591
url http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.publisher.program.fl_str_mv Programa de PÃs-GraduaÃÃo em Farmacologia
dc.publisher.initials.fl_str_mv UFC
dc.publisher.country.fl_str_mv BR
publisher.none.fl_str_mv Universidade Federal do CearÃ
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFC
instname:Universidade Federal do Ceará
instacron:UFC
reponame_str Biblioteca Digital de Teses e Dissertações da UFC
collection Biblioteca Digital de Teses e Dissertações da UFC
instname_str Universidade Federal do Ceará
instacron_str UFC
institution UFC
repository.name.fl_str_mv -
repository.mail.fl_str_mv mail@mail.com
_version_ 1643295227461500928