Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106518
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dc.contributor.authorPreguiça, Inês-
dc.contributor.authorAlves, André-
dc.contributor.authorNunes, Sara-
dc.contributor.authorGomes, Pedro-
dc.contributor.authorFernandes, Rosa-
dc.contributor.authorViana, Sofia D.-
dc.contributor.authorReis, Flávio-
dc.date.accessioned2023-04-06T08:36:21Z-
dc.date.available2023-04-06T08:36:21Z-
dc.date.issued2020-01-18-
dc.identifier.issn2072-6643-
dc.identifier.urihttps://hdl.handle.net/10316/106518-
dc.description.abstractUnhealthy dietary habits are major modifiable risk factors for the development of type 2 diabetes mellitus, a metabolic disease with increasing prevalence and serious consequences. Microvascular complications of diabetes, namely diabetic peripheral neuropathy (DPN), retinopathy (DR), and nephropathy (DN), are associated with high morbidity rates and a heavy social and economic burden. Currently, available therapeutic options to counter the evolution of diabetic microvascular complications are clearly insufficient, which strongly recommends further research. Animal models are essential tools to dissect the molecular mechanisms underlying disease progression, to unravel new therapeutic targets, as well as to evaluate the efficacy of new drugs and/or novel therapeutic approaches. However, choosing the best animal model is challenging due to the large number of factors that need to be considered. This is particularly relevant for models induced by dietary modifications, which vary markedly in terms of macronutrient composition. In this article, we revisit the rodent models of diet-induced DPN, DR, and DN, critically comparing the main features of these microvascular complications in humans and the criteria for their diagnosis with the parameters that have been used in preclinical research using rodent models, considering the possible need for factors which can accelerate or aggravate these conditions.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationCENTRO-01-0145-FEDER-000012-HealthyAging2020pt
dc.relationUID/NEU/ 04539/2013pt
dc.relationUID/NEU/04539/2019pt
dc.relationinfo:eu-repo/grantAgreement/SFRH/BD/109017/2015pt
dc.relationPTDC/SAU-NUT/31712/2017pt
dc.relationPOCI-01-0145-FEDER-007440pt
dc.relationPOCI-01-0145-FEDER-031712pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjecttype 2 diabetes mellituspt
dc.subjectmicrovascular complicationspt
dc.subjectdiabetic peripheral neuropathypt
dc.subjectdiabetic retinopathypt
dc.subjectdiabetic nephropathypt
dc.subjectrodent modelspt
dc.subjectdiet-inducedpt
dc.titleDiet-Induced Rodent Models of Diabetic Peripheral Neuropathy, Retinopathy and Nephropathypt
dc.typearticlept
degois.publication.firstPage250pt
degois.publication.issue1pt
degois.publication.titleNutrientspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/nu12010250-
degois.publication.volume12pt
dc.date.embargo2020-01-18*
dc.identifier.pmid31963709-
uc.date.periodoEmbargo0pt
dc.identifier.eissn2072-6643-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
item.openairetypearticle-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-1766-9133-
crisitem.author.orcid0000-0001-7828-2296-
crisitem.author.orcid0000-0002-1316-1319-
crisitem.author.orcid0000-0003-3401-9554-
Appears in Collections:I&D ICBR - Artigos em Revistas Internacionais
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