Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats

Detalhes bibliográficos
Autor(a) principal: Ever Elias Mena Laura
Data de Publicação: 2019
Tipo de documento: Tese
Idioma: eng
Título da fonte: Biblioteca Digital de Teses e Dissertações da USP
Texto Completo: https://doi.org/10.11606/T.25.2019.tde-05102021-115649
Resumo: Objectives: We studied the periodontal response to orthodontic forces in type 1 diabetic rats (T1D) treated with insulin and metformin and type 2 diabetic rats (T2D) treated exclusively with metformin (MET). Materials and methods: In article 1, T1D was induced by single injection of streptozotocin (STZ), whereas in article 2, T2D was induced by 90 days of high fat diet (HFD) with a single and low dose administration of STZ. In both articles 1 and 2 as soon as diabetes was induced in rats, an orthodontic appliance was installed to move the right upper first molar mesially for periods of 0, 3, 7, and 14 days. Samples were analyzed by micro-CT histomorphometry and immunohistochemistry for TRAP + cells. Results: Diabetic induction with STZ on the one hand, and HDF plus STZ on the other resulted in pathognomonic signs of T1D (hyperglycemia) and T2D (increase in body mass, insulin resistance, glucose intolerance and hyperglycemia), respectively. The addition of MET decreased blood glucose to values close to NG and better than insulin alone in T1D. In T2D, MET significantly reduced blood glucose, insulin tolerance and glucose tolerance. During orthodontic movement (OTM), T1D and T2D led to greater mesial movement, mesial inclination, mesial rotation (mesioversion), periodontal ligament spacing associated to a larger number of TRAP+ cells, and bone resorption surfaces (ORS) which were significantly reduced by MET on T2D and MET added to insulin on T1D. T2D presented maxillary osteoporosis or reduced BV / TV and BA / TA before OTM, but in T1D this occurred during OTM, however these effects were counteracted by MET. Yet, a different pattern of OTM occurs in T1D and T2D due to different bone density, and extrusion versus intrusion presented in T1D and T2D, respectively. Conclusion: The addition of metformin to insulin in T1D or single administration in T2D reduces the adverse effects on periodontal tissues during orthodontic movement in type 1 and 2 diabetic rats.
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spelling info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats Impacto da metformina na resposta periodontal à forças ortodônticas em ratos diabéticos tipo 1 e 2 2019-10-07Gerson Francisco de AssisFlavio Augusto Cardoso de FariaGabriela GennaroRenato MartinsEver Elias Mena LauraUniversidade de São PauloCiências Odontológicas AplicadasUSPBR Diabetes tipo 1 Diabetes tipo 2 Metformin Metformina Movimento dentário ortodôntico Orthodontic tooth movement Periodontium Periodonto Type 1 diabetes Type 2 diabetes Objectives: We studied the periodontal response to orthodontic forces in type 1 diabetic rats (T1D) treated with insulin and metformin and type 2 diabetic rats (T2D) treated exclusively with metformin (MET). Materials and methods: In article 1, T1D was induced by single injection of streptozotocin (STZ), whereas in article 2, T2D was induced by 90 days of high fat diet (HFD) with a single and low dose administration of STZ. In both articles 1 and 2 as soon as diabetes was induced in rats, an orthodontic appliance was installed to move the right upper first molar mesially for periods of 0, 3, 7, and 14 days. Samples were analyzed by micro-CT histomorphometry and immunohistochemistry for TRAP + cells. Results: Diabetic induction with STZ on the one hand, and HDF plus STZ on the other resulted in pathognomonic signs of T1D (hyperglycemia) and T2D (increase in body mass, insulin resistance, glucose intolerance and hyperglycemia), respectively. The addition of MET decreased blood glucose to values close to NG and better than insulin alone in T1D. In T2D, MET significantly reduced blood glucose, insulin tolerance and glucose tolerance. During orthodontic movement (OTM), T1D and T2D led to greater mesial movement, mesial inclination, mesial rotation (mesioversion), periodontal ligament spacing associated to a larger number of TRAP+ cells, and bone resorption surfaces (ORS) which were significantly reduced by MET on T2D and MET added to insulin on T1D. T2D presented maxillary osteoporosis or reduced BV / TV and BA / TA before OTM, but in T1D this occurred during OTM, however these effects were counteracted by MET. Yet, a different pattern of OTM occurs in T1D and T2D due to different bone density, and extrusion versus intrusion presented in T1D and T2D, respectively. Conclusion: The addition of metformin to insulin in T1D or single administration in T2D reduces the adverse effects on periodontal tissues during orthodontic movement in type 1 and 2 diabetic rats. Objetivos: Nós estudamos a resposta periodontal às forças ortodônticas em ratos diabéticos tipo 1 (T1D) tratados com metformina (MET) adicionada à insulina, e ratos diabéticos tipo 2 (T2D) tratados exclusivamente com metformina. Materiais e métodos: No artigo 1 a T1D foi induzida por injeção única de estreptozotocina (STZ), enquanto que no artigo 2 a T2D foi induzida por alimentação rica em gordura (HFD) por 90 dias e administração de dose única e baixa de STZ. Em ambos artigos 1 e 2 assim que a diabetes foi induzida nos ratos, um aparelho ortodóntico foi instalado para movimentar o primeiro molar superior direito mesialmente por períodos de 0, 3, 7, e 14 dias. As amostras foram analisadas por micro-CT histomorfometria e imunohistoquímica para células TRAP+. Resultados: A indução diabética, com STZ por um lado, e HDF mais STZ por outro, resultou em signos patognomônicos da T1D (hiperglicemia) e T2D (aumento da massa corporal, resistência insulina, intolerância à glicose e hiperglicemia), respectivamente. A adição de MET diminuiu a glicemia a valores próximos do NG e melhor do que só insulina na T1D. Na T2D a MET reduziu significantemente a glicemia, tolerância à insulina e tolerância à glicose. Durante o movimento ortodôntico (MO), T1D e T2D levaram a maior movimento mesial, inclinação mesial, rotação mesial (mesioversão), espaçamento do ligamento periodontal associado a maior numero de células TRAP+ e superfícies de reabsorção óssea (ORS) os quais foram significantemente reduzidos pela MET na T2D e a adição de MET à insulina na T1D. A T2D apresentou osteoporose maxilar ou BV/TV e BA/TA reduzido antes do MO, mas no T1D, isso ocorreu durante o MO, porem esses efeitos foram contrariados pela MET. Ainda um diferente padrão de MO ocorre na T1D e T2D pela diferente densidade óssea, e extrusão versus a intrusão apresentadas na T1D e T2D, respectivamente. Conclusão: A adição de metformina à insulina na T1D ou administração única na T2D reduzem os efeitos adversos no periodonto durante o movimento ortodôntico em ratos diabéticos tipo 1 e 2. https://doi.org/10.11606/T.25.2019.tde-05102021-115649info:eu-repo/semantics/openAccessengreponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USP2023-12-21T18:17:10Zoai:teses.usp.br:tde-05102021-115649Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212023-12-22T12:11:14.354353Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.en.fl_str_mv Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
dc.title.alternative.pt.fl_str_mv Impacto da metformina na resposta periodontal à forças ortodônticas em ratos diabéticos tipo 1 e 2
title Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
spellingShingle Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
Ever Elias Mena Laura
title_short Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
title_full Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
title_fullStr Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
title_full_unstemmed Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
title_sort Impact of metformin on periodontal response to orthodontic forces in type 1 and 2 diabetic rats
author Ever Elias Mena Laura
author_facet Ever Elias Mena Laura
author_role author
dc.contributor.advisor1.fl_str_mv Gerson Francisco de Assis
dc.contributor.referee1.fl_str_mv Flavio Augusto Cardoso de Faria
dc.contributor.referee2.fl_str_mv Gabriela Gennaro
dc.contributor.referee3.fl_str_mv Renato Martins
dc.contributor.author.fl_str_mv Ever Elias Mena Laura
contributor_str_mv Gerson Francisco de Assis
Flavio Augusto Cardoso de Faria
Gabriela Gennaro
Renato Martins
description Objectives: We studied the periodontal response to orthodontic forces in type 1 diabetic rats (T1D) treated with insulin and metformin and type 2 diabetic rats (T2D) treated exclusively with metformin (MET). Materials and methods: In article 1, T1D was induced by single injection of streptozotocin (STZ), whereas in article 2, T2D was induced by 90 days of high fat diet (HFD) with a single and low dose administration of STZ. In both articles 1 and 2 as soon as diabetes was induced in rats, an orthodontic appliance was installed to move the right upper first molar mesially for periods of 0, 3, 7, and 14 days. Samples were analyzed by micro-CT histomorphometry and immunohistochemistry for TRAP + cells. Results: Diabetic induction with STZ on the one hand, and HDF plus STZ on the other resulted in pathognomonic signs of T1D (hyperglycemia) and T2D (increase in body mass, insulin resistance, glucose intolerance and hyperglycemia), respectively. The addition of MET decreased blood glucose to values close to NG and better than insulin alone in T1D. In T2D, MET significantly reduced blood glucose, insulin tolerance and glucose tolerance. During orthodontic movement (OTM), T1D and T2D led to greater mesial movement, mesial inclination, mesial rotation (mesioversion), periodontal ligament spacing associated to a larger number of TRAP+ cells, and bone resorption surfaces (ORS) which were significantly reduced by MET on T2D and MET added to insulin on T1D. T2D presented maxillary osteoporosis or reduced BV / TV and BA / TA before OTM, but in T1D this occurred during OTM, however these effects were counteracted by MET. Yet, a different pattern of OTM occurs in T1D and T2D due to different bone density, and extrusion versus intrusion presented in T1D and T2D, respectively. Conclusion: The addition of metformin to insulin in T1D or single administration in T2D reduces the adverse effects on periodontal tissues during orthodontic movement in type 1 and 2 diabetic rats.
publishDate 2019
dc.date.issued.fl_str_mv 2019-10-07
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.11606/T.25.2019.tde-05102021-115649
url https://doi.org/10.11606/T.25.2019.tde-05102021-115649
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade de São Paulo
dc.publisher.program.fl_str_mv Ciências Odontológicas Aplicadas
dc.publisher.initials.fl_str_mv USP
dc.publisher.country.fl_str_mv BR
publisher.none.fl_str_mv Universidade de São Paulo
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da USP
instname:Universidade de São Paulo (USP)
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instname_str Universidade de São Paulo (USP)
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reponame_str Biblioteca Digital de Teses e Dissertações da USP
collection Biblioteca Digital de Teses e Dissertações da USP
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)
repository.mail.fl_str_mv virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br
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