Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article
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Publication Date: | 2017 |
Other Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10362/152348 |
Summary: | This study was supported by Portuguese Foundation for Science and Technology (projectUID/NEU/04539/2013), QREN-COMPETE (project DoIT- Diamarker: a consortium for the discovery of novel biomarker in diabetes), POCI-01-0145-FEDER-007440 and by the Faculty of Medicine, University of Coimbra. T. R. and P. M. are supported by a PhD (SFRH/BD/101172/2014) and a Post-Doc Grant (SFRH/BPD/104881/2014). This study was granted by the Portuguese Society of Diabetology (Portuguese National Prize of Diabetes). |
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Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 articleGeneralSDG 3 - Good Health and Well-beingThis study was supported by Portuguese Foundation for Science and Technology (projectUID/NEU/04539/2013), QREN-COMPETE (project DoIT- Diamarker: a consortium for the discovery of novel biomarker in diabetes), POCI-01-0145-FEDER-007440 and by the Faculty of Medicine, University of Coimbra. T. R. and P. M. are supported by a PhD (SFRH/BD/101172/2014) and a Post-Doc Grant (SFRH/BPD/104881/2014). This study was granted by the Portuguese Society of Diabetology (Portuguese National Prize of Diabetes).Microvascular dysfunction has been suggested to trigger adipose tissue dysfunction in obesity. This study investigates the hypothesis that glycation impairs microvascular architecture and expandability with an impact on insulin signalling. Animal models supplemented with methylglyoxal (MG), maintained with a high-fat diet (HFD) or both (HFDMG) were studied for periepididymal adipose (pEAT) tissue hypoxia and local and systemic insulin resistance. Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) was used to quantify blood flow in vivo, showing MG-induced reduction of pEAT blood flow. Increased adipocyte size and leptin secretion were observed only in rats feeding the high-fat diet, without the development of hypoxia. In turn, hypoxia was only observed when MG was combined (HFDMG group), being associated with impaired activation of the insulin receptor (Tyr1163), glucose intolerance and systemic and muscle insulin resistance. Accordingly, the adipose tissue angiogenic assay has shown decreased capillarization after dose-dependent MG exposure and glyoxalase-1 inhibition. Thus, glycation impairs adipose tissue capillarization and blood flow, hampering its expandability during a high-fat diet challenge and leading to hypoxia and insulin resistance. Such events have systemic repercussions in glucose metabolism and may lead to the onset of unhealthy obesity and progression to type 2 diabetes.Centro de Estudos de Doenças Crónicas (CEDOC)NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)RUNRodrigues, TiagoMatafome, PauloSereno, JoséAlmeida, JoséCastelhano, JoãoGamas, LuísNeves, ChristianGonçalves, SóniaCarvalho, CatarinaArslanagic, AminaWilcken, ElinorFonseca, RitaSimões, IldaV Conde, SilviaCastelo-Branco, MiguelSeiça, Raquel2023-05-02T22:12:54Z2017-12-012017-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/152348eng2045-2322PURE: 59822630https://doi.org/10.1038/s41598-017-01730-3info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-05-26T01:40:47Zoai:run.unl.pt:10362/152348Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:41:26.780025Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
title |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
spellingShingle |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article Rodrigues, Tiago General SDG 3 - Good Health and Well-being |
title_short |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
title_full |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
title_fullStr |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
title_full_unstemmed |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
title_sort |
Methylglyoxal-induced glycation changes adipose tissue vascular architecture, flow and expansion, leading to insulin resistance /692/163/2743/2037 /692/308/1426 /13/106 /59 /59/36 article |
author |
Rodrigues, Tiago |
author_facet |
Rodrigues, Tiago Matafome, Paulo Sereno, José Almeida, José Castelhano, João Gamas, Luís Neves, Christian Gonçalves, Sónia Carvalho, Catarina Arslanagic, Amina Wilcken, Elinor Fonseca, Rita Simões, Ilda V Conde, Silvia Castelo-Branco, Miguel Seiça, Raquel |
author_role |
author |
author2 |
Matafome, Paulo Sereno, José Almeida, José Castelhano, João Gamas, Luís Neves, Christian Gonçalves, Sónia Carvalho, Catarina Arslanagic, Amina Wilcken, Elinor Fonseca, Rita Simões, Ilda V Conde, Silvia Castelo-Branco, Miguel Seiça, Raquel |
author2_role |
author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Centro de Estudos de Doenças Crónicas (CEDOC) NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM) RUN |
dc.contributor.author.fl_str_mv |
Rodrigues, Tiago Matafome, Paulo Sereno, José Almeida, José Castelhano, João Gamas, Luís Neves, Christian Gonçalves, Sónia Carvalho, Catarina Arslanagic, Amina Wilcken, Elinor Fonseca, Rita Simões, Ilda V Conde, Silvia Castelo-Branco, Miguel Seiça, Raquel |
dc.subject.por.fl_str_mv |
General SDG 3 - Good Health and Well-being |
topic |
General SDG 3 - Good Health and Well-being |
description |
This study was supported by Portuguese Foundation for Science and Technology (projectUID/NEU/04539/2013), QREN-COMPETE (project DoIT- Diamarker: a consortium for the discovery of novel biomarker in diabetes), POCI-01-0145-FEDER-007440 and by the Faculty of Medicine, University of Coimbra. T. R. and P. M. are supported by a PhD (SFRH/BD/101172/2014) and a Post-Doc Grant (SFRH/BPD/104881/2014). This study was granted by the Portuguese Society of Diabetology (Portuguese National Prize of Diabetes). |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-12-01 2017-12-01T00:00:00Z 2023-05-02T22:12:54Z |
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://hdl.handle.net/10362/152348 |
url |
http://hdl.handle.net/10362/152348 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2045-2322 PURE: 59822630 https://doi.org/10.1038/s41598-017-01730-3 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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