Dipeptidyl peptidase IV inhibitor improves the salivary gland histology of spontaneously diabetic mice
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , |
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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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:29462024-08-05T20:03:24.773172Repositório 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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1808129155413311488 |