Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats
Autor(a) principal: | |
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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. |
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Biblioteca Digital de Teses e Dissertações da UFC |
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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 |
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openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal do Cearà |
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 |
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Universidade Federal do Cearà |
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reponame:Biblioteca Digital de Teses e Dissertações da UFC instname:Universidade Federal do Ceará instacron:UFC |
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Biblioteca Digital de Teses e Dissertações da UFC |
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Biblioteca Digital de Teses e Dissertações da UFC |
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Universidade Federal do Ceará |
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UFC |
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UFC |
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mail@mail.com |
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