Pancreatic islet response to diabetes during pregnancy in rats
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.lfs.2018.10.046 http://hdl.handle.net/11449/188257 |
Resumo: | Aims: The objective of this study was to assess the mechanisms underlying pancreatic islet adaptation in diabetic mothers and their pups. Additionally, the influence of pancreatic adaptations on maternal reproductive performance was also investigated. Main methods: Wistar rats were injected with streptozotocin for diabetes induction. At adulthood (3 months), all animals underwent an oral glucose tolerance test (OGTT) for glucose assessment as an inclusion criterion. Following, the animals were mated. At day 18 of pregnancy, the mothers were killed for blood collect ion to determine fasting insulin and glucagon concentrations. The pancreas was removed and processed for the immunohistochemical analysis of insulin, glucagon, somatostatin, Ki-67 and PDX-1, superoxide dismutase 1 (SOD-1), glutathione peroxidase (GSH-Px) and malondialdehyde (MDA). The pregnant uterus was also collected for the evaluation of embryofetal loss. Key findings: The diabetic rats showed increased glucose, serum glucagon and insulin concentrations, and embryofetal loss rates. They also showed a reduction in pancreatic islets area and percentage of cells stained for insulin, increased the percentage of non-β cells (alpha e delta cells) stained for Ki-67, glucagon, and somatostatin. Moreover, the cells stained for somatostatin were spread across the islets and showed stronger staining for MDA and weaker staining for GSH-Px. Significance: Diabetes leads to adaptive responses from the endocrine pancreas in pregnancy that especially involves non-β cells, modifying the mantle-core structure. Nonetheless, these adaptations are not enough for glucose homeostasis and affect the maternal environment, which in turn impairs fetal development. |
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Pancreatic islet response to diabetes during pregnancy in ratsAnimal modelGestationHyperglycemiaPancreasAims: The objective of this study was to assess the mechanisms underlying pancreatic islet adaptation in diabetic mothers and their pups. Additionally, the influence of pancreatic adaptations on maternal reproductive performance was also investigated. Main methods: Wistar rats were injected with streptozotocin for diabetes induction. At adulthood (3 months), all animals underwent an oral glucose tolerance test (OGTT) for glucose assessment as an inclusion criterion. Following, the animals were mated. At day 18 of pregnancy, the mothers were killed for blood collect ion to determine fasting insulin and glucagon concentrations. The pancreas was removed and processed for the immunohistochemical analysis of insulin, glucagon, somatostatin, Ki-67 and PDX-1, superoxide dismutase 1 (SOD-1), glutathione peroxidase (GSH-Px) and malondialdehyde (MDA). The pregnant uterus was also collected for the evaluation of embryofetal loss. Key findings: The diabetic rats showed increased glucose, serum glucagon and insulin concentrations, and embryofetal loss rates. They also showed a reduction in pancreatic islets area and percentage of cells stained for insulin, increased the percentage of non-β cells (alpha e delta cells) stained for Ki-67, glucagon, and somatostatin. Moreover, the cells stained for somatostatin were spread across the islets and showed stronger staining for MDA and weaker staining for GSH-Px. Significance: Diabetes leads to adaptive responses from the endocrine pancreas in pregnancy that especially involves non-β cells, modifying the mantle-core structure. Nonetheless, these adaptations are not enough for glucose homeostasis and affect the maternal environment, which in turn impairs fetal development.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Laboratory of Experimental Research on Gynecology and Obstetrics Gynecology Obstetrics and Mastology Post Graduate Course Botucatu Medical School Univ Estadual Paulista_UnespDeVry Ruy Barbosa School (DeVry Brazil Group)Laboratory of System Physiology and Reproductive Toxicology Institute of Biological and Health Sciences Federal University of Mato Grosso (UFMT)Department of Morphology Botucatu Bioscience Institute Univ Estadual Paulista_UnespBiomedical Research Centre Universidad de ValparaísoLaboratory of Experimental Research on Gynecology and Obstetrics Gynecology Obstetrics and Mastology Post Graduate Course Botucatu Medical School Univ Estadual Paulista_UnespDepartment of Morphology Botucatu Bioscience Institute Univ Estadual Paulista_UnespFAPESP: 2011/18519-7Universidade Estadual Paulista (Unesp)DeVry Ruy Barbosa School (DeVry Brazil Group)Federal University of Mato Grosso (UFMT)Universidad de ValparaísoGallego, Franciane Quintanilha [UNESP]Sinzato, Yuri Karen [UNESP]Miranda, Carolina Abreu [UNESP]Iessi, Isabela Lovizutto [UNESP]Dallaqua, BrunaVolpato, Gustavo TadeuScarano, Wellerson Rodrigo [UNESP]SanMartín, SebastianDamasceno, Débora Cristina [UNESP]2019-10-06T16:02:14Z2019-10-06T16:02:14Z2018-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1-10http://dx.doi.org/10.1016/j.lfs.2018.10.046Life Sciences, v. 214, p. 1-10.1879-06310024-3205http://hdl.handle.net/11449/18825710.1016/j.lfs.2018.10.0462-s2.0-85055481741Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLife Sciencesinfo:eu-repo/semantics/openAccess2024-08-16T14:07:22Zoai:repositorio.unesp.br:11449/188257Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-16T14:07:22Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Pancreatic islet response to diabetes during pregnancy in rats |
title |
Pancreatic islet response to diabetes during pregnancy in rats |
spellingShingle |
Pancreatic islet response to diabetes during pregnancy in rats Gallego, Franciane Quintanilha [UNESP] Animal model Gestation Hyperglycemia Pancreas |
title_short |
Pancreatic islet response to diabetes during pregnancy in rats |
title_full |
Pancreatic islet response to diabetes during pregnancy in rats |
title_fullStr |
Pancreatic islet response to diabetes during pregnancy in rats |
title_full_unstemmed |
Pancreatic islet response to diabetes during pregnancy in rats |
title_sort |
Pancreatic islet response to diabetes during pregnancy in rats |
author |
Gallego, Franciane Quintanilha [UNESP] |
author_facet |
Gallego, Franciane Quintanilha [UNESP] Sinzato, Yuri Karen [UNESP] Miranda, Carolina Abreu [UNESP] Iessi, Isabela Lovizutto [UNESP] Dallaqua, Bruna Volpato, Gustavo Tadeu Scarano, Wellerson Rodrigo [UNESP] SanMartín, Sebastian Damasceno, Débora Cristina [UNESP] |
author_role |
author |
author2 |
Sinzato, Yuri Karen [UNESP] Miranda, Carolina Abreu [UNESP] Iessi, Isabela Lovizutto [UNESP] Dallaqua, Bruna Volpato, Gustavo Tadeu Scarano, Wellerson Rodrigo [UNESP] SanMartín, Sebastian Damasceno, Débora Cristina [UNESP] |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) DeVry Ruy Barbosa School (DeVry Brazil Group) Federal University of Mato Grosso (UFMT) Universidad de Valparaíso |
dc.contributor.author.fl_str_mv |
Gallego, Franciane Quintanilha [UNESP] Sinzato, Yuri Karen [UNESP] Miranda, Carolina Abreu [UNESP] Iessi, Isabela Lovizutto [UNESP] Dallaqua, Bruna Volpato, Gustavo Tadeu Scarano, Wellerson Rodrigo [UNESP] SanMartín, Sebastian Damasceno, Débora Cristina [UNESP] |
dc.subject.por.fl_str_mv |
Animal model Gestation Hyperglycemia Pancreas |
topic |
Animal model Gestation Hyperglycemia Pancreas |
description |
Aims: The objective of this study was to assess the mechanisms underlying pancreatic islet adaptation in diabetic mothers and their pups. Additionally, the influence of pancreatic adaptations on maternal reproductive performance was also investigated. Main methods: Wistar rats were injected with streptozotocin for diabetes induction. At adulthood (3 months), all animals underwent an oral glucose tolerance test (OGTT) for glucose assessment as an inclusion criterion. Following, the animals were mated. At day 18 of pregnancy, the mothers were killed for blood collect ion to determine fasting insulin and glucagon concentrations. The pancreas was removed and processed for the immunohistochemical analysis of insulin, glucagon, somatostatin, Ki-67 and PDX-1, superoxide dismutase 1 (SOD-1), glutathione peroxidase (GSH-Px) and malondialdehyde (MDA). The pregnant uterus was also collected for the evaluation of embryofetal loss. Key findings: The diabetic rats showed increased glucose, serum glucagon and insulin concentrations, and embryofetal loss rates. They also showed a reduction in pancreatic islets area and percentage of cells stained for insulin, increased the percentage of non-β cells (alpha e delta cells) stained for Ki-67, glucagon, and somatostatin. Moreover, the cells stained for somatostatin were spread across the islets and showed stronger staining for MDA and weaker staining for GSH-Px. Significance: Diabetes leads to adaptive responses from the endocrine pancreas in pregnancy that especially involves non-β cells, modifying the mantle-core structure. Nonetheless, these adaptations are not enough for glucose homeostasis and affect the maternal environment, which in turn impairs fetal development. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-01 2019-10-06T16:02:14Z 2019-10-06T16:02:14Z |
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.lfs.2018.10.046 Life Sciences, v. 214, p. 1-10. 1879-0631 0024-3205 http://hdl.handle.net/11449/188257 10.1016/j.lfs.2018.10.046 2-s2.0-85055481741 |
url |
http://dx.doi.org/10.1016/j.lfs.2018.10.046 http://hdl.handle.net/11449/188257 |
identifier_str_mv |
Life Sciences, v. 214, p. 1-10. 1879-0631 0024-3205 10.1016/j.lfs.2018.10.046 2-s2.0-85055481741 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Life Sciences |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1-10 |
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 |
|
_version_ |
1808128161245822976 |