Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice

Detalhes bibliográficos
Autor(a) principal: Da Silva Faria, Ana Luyza Domingues
Data de Publicação: 2013
Outros Autores: Dias, Marco Antônio, Leme, Vinicius Barichelo, Mayoral, Éber Emanuel, Da Silva, Rodrigo Eduardo, Mâncio, Rafael Dias, Ferreira Junior, Rui Seabra [UNESP], Caldeira, Eduardo José
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.archoralbio.2012.09.015
http://hdl.handle.net/11449/75752
Resumo: Objectives: The incretin-based therapy might be effective in patients possessing certain levels of preserved pancreatic beta-cells. However, doubts still exist regarding the efficacy of this atment in the recovery of tissues damaged by type 1 diabetes. Thus, the objective of this study was to evaluate the treatment with MK0431 in salivary glands of spontaneously diabetic mice, focusing mainly on the possible therapeutic and hypoglycaemic effects of this dipeptidyl peptidase IV inhibitor in the recovery of these salivary tissues. Methods and results: Twenty mice were divided into two groups of 10 animals each: group I (NOD diabetic/untreated) and group II (NOD diabetic MK0431/treated). The group II was treated during 4 weeks with MK0431 mixed in the food. The group I was maintained in the same way without receiving, however, any treatment. Glucose levels were monitored during treatment and salivary glands samples were collected at the end of treatment for the histological examination under both transmitted and polarized light microscopy. High glucose levels were observed in untreated animals, while in animals with treatment, reduction of these levels was observed. Tissue restructuring was also observed in animals submitted to therapy with MK0431, mainly in relation to the attempt to extracellular matrix reorganization. Conclusions: According to results, the treatment with this dipeptidyl peptidase IV inhibitor contributed to the general homeostasis of the organism and to the reestablishment of both epithelial and stromal compartments which were damaged by the hyperglycaemic condition, demonstrating that the incretin-based therapy may be an important complementary treatment for the type 1 diabetic condition. © 2012 Elsevier Ltd.
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spelling Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic miceComplementary therapiesDiabetes mellitusSalivary glandsAnimaliaMusObjectives: The incretin-based therapy might be effective in patients possessing certain levels of preserved pancreatic beta-cells. However, doubts still exist regarding the efficacy of this atment in the recovery of tissues damaged by type 1 diabetes. Thus, the objective of this study was to evaluate the treatment with MK0431 in salivary glands of spontaneously diabetic mice, focusing mainly on the possible therapeutic and hypoglycaemic effects of this dipeptidyl peptidase IV inhibitor in the recovery of these salivary tissues. Methods and results: Twenty mice were divided into two groups of 10 animals each: group I (NOD diabetic/untreated) and group II (NOD diabetic MK0431/treated). The group II was treated during 4 weeks with MK0431 mixed in the food. The group I was maintained in the same way without receiving, however, any treatment. Glucose levels were monitored during treatment and salivary glands samples were collected at the end of treatment for the histological examination under both transmitted and polarized light microscopy. High glucose levels were observed in untreated animals, while in animals with treatment, reduction of these levels was observed. Tissue restructuring was also observed in animals submitted to therapy with MK0431, mainly in relation to the attempt to extracellular matrix reorganization. Conclusions: According to results, the treatment with this dipeptidyl peptidase IV inhibitor contributed to the general homeostasis of the organism and to the reestablishment of both epithelial and stromal compartments which were damaged by the hyperglycaemic condition, demonstrating that the incretin-based therapy may be an important complementary treatment for the type 1 diabetic condition. © 2012 Elsevier Ltd.Tissue Morphology Laboratory Department of Morphology and Basic Pathology Faculty of Medicine of Jundiaí, FMJ, Rua Francisco Telles, 250, Vila Arens, Jundiaí, São PauloCEVAP São Paulo State University UNESP, Botucatu, São PauloCEVAP São Paulo State University UNESP, Botucatu, São PauloFaculdade de Medicina de Jundiaí (FMJ)Universidade Estadual Paulista (Unesp)Da Silva Faria, Ana Luyza DominguesDias, Marco AntônioLeme, Vinicius BaricheloMayoral, Éber EmanuelDa Silva, Rodrigo EduardoMâncio, Rafael DiasFerreira Junior, Rui Seabra [UNESP]Caldeira, Eduardo José2014-05-27T11:29:48Z2014-05-27T11:29:48Z2013-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article755-761application/pdfhttp://dx.doi.org/10.1016/j.archoralbio.2012.09.015Archives of Oral Biology, v. 58, n. 7, p. 755-761, 2013.0003-9969http://hdl.handle.net/11449/7575210.1016/j.archoralbio.2012.09.015WOS:0003204175000022-s2.0-848782308482-s2.0-84878230848.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengArchives of Oral Biology2.0500,752info:eu-repo/semantics/openAccess2024-04-11T15:28:26Zoai:repositorio.unesp.br:11449/75752Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-04-11T15:28:26Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
title Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
spellingShingle Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
Da Silva Faria, Ana Luyza Domingues
Complementary therapies
Diabetes mellitus
Salivary glands
Animalia
Mus
title_short Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
title_full Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
title_fullStr Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
title_full_unstemmed Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
title_sort Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
author Da Silva Faria, Ana Luyza Domingues
author_facet Da Silva Faria, Ana Luyza Domingues
Dias, Marco Antônio
Leme, Vinicius Barichelo
Mayoral, Éber Emanuel
Da Silva, Rodrigo Eduardo
Mâncio, Rafael Dias
Ferreira Junior, Rui Seabra [UNESP]
Caldeira, Eduardo José
author_role author
author2 Dias, Marco Antônio
Leme, Vinicius Barichelo
Mayoral, Éber Emanuel
Da Silva, Rodrigo Eduardo
Mâncio, Rafael Dias
Ferreira Junior, Rui Seabra [UNESP]
Caldeira, Eduardo José
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Faculdade de Medicina de Jundiaí (FMJ)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Da Silva Faria, Ana Luyza Domingues
Dias, Marco Antônio
Leme, Vinicius Barichelo
Mayoral, Éber Emanuel
Da Silva, Rodrigo Eduardo
Mâncio, Rafael Dias
Ferreira Junior, Rui Seabra [UNESP]
Caldeira, Eduardo José
dc.subject.por.fl_str_mv Complementary therapies
Diabetes mellitus
Salivary glands
Animalia
Mus
topic Complementary therapies
Diabetes mellitus
Salivary glands
Animalia
Mus
description Objectives: The incretin-based therapy might be effective in patients possessing certain levels of preserved pancreatic beta-cells. However, doubts still exist regarding the efficacy of this atment in the recovery of tissues damaged by type 1 diabetes. Thus, the objective of this study was to evaluate the treatment with MK0431 in salivary glands of spontaneously diabetic mice, focusing mainly on the possible therapeutic and hypoglycaemic effects of this dipeptidyl peptidase IV inhibitor in the recovery of these salivary tissues. Methods and results: Twenty mice were divided into two groups of 10 animals each: group I (NOD diabetic/untreated) and group II (NOD diabetic MK0431/treated). The group II was treated during 4 weeks with MK0431 mixed in the food. The group I was maintained in the same way without receiving, however, any treatment. Glucose levels were monitored during treatment and salivary glands samples were collected at the end of treatment for the histological examination under both transmitted and polarized light microscopy. High glucose levels were observed in untreated animals, while in animals with treatment, reduction of these levels was observed. Tissue restructuring was also observed in animals submitted to therapy with MK0431, mainly in relation to the attempt to extracellular matrix reorganization. Conclusions: According to results, the treatment with this dipeptidyl peptidase IV inhibitor contributed to the general homeostasis of the organism and to the reestablishment of both epithelial and stromal compartments which were damaged by the hyperglycaemic condition, demonstrating that the incretin-based therapy may be an important complementary treatment for the type 1 diabetic condition. © 2012 Elsevier Ltd.
publishDate 2013
dc.date.none.fl_str_mv 2013-07-01
2014-05-27T11:29:48Z
2014-05-27T11:29:48Z
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/10.1016/j.archoralbio.2012.09.015
Archives of Oral Biology, v. 58, n. 7, p. 755-761, 2013.
0003-9969
http://hdl.handle.net/11449/75752
10.1016/j.archoralbio.2012.09.015
WOS:000320417500002
2-s2.0-84878230848
2-s2.0-84878230848.pdf
url http://dx.doi.org/10.1016/j.archoralbio.2012.09.015
http://hdl.handle.net/11449/75752
identifier_str_mv Archives of Oral Biology, v. 58, n. 7, p. 755-761, 2013.
0003-9969
10.1016/j.archoralbio.2012.09.015
WOS:000320417500002
2-s2.0-84878230848
2-s2.0-84878230848.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Archives of Oral Biology
2.050
0,752
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 755-761
application/pdf
dc.source.none.fl_str_mv Scopus
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
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