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dc.contributor.authorGarcia-Carrizo, Francisco
dc.contributor.authorPriego, Teresa
dc.contributor.authorSzostaczuk, Nara
dc.contributor.authorPalou, Andreu
dc.contributor.authorPicó, Catalina
dc.date.accessioned2024-07-11T09:10:36Z
dc.date.available2024-07-11T09:10:36Z
dc.date.issued2017-07-11
dc.identifier.citationGarcia-Carrizo F, Priego T, Szostaczuk N, Palou Oliver A, Pico C. Sexual Dimorphism in the Age-Induced Insulin Resistance, Liver Steatosis, and Adipose Tissue Function in Rats. Front Physiol. 2017 Jul 11;8:445.en
dc.identifier.issn1664-042X
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/9747
dc.identifier.urihttp://hdl.handle.net/20.500.12105/20440
dc.description.abstractAge-linked metabolic disturbances, such as liver steatosis and insulin resistance, show greater prevalence in men than in women. Thus, our aim was to analyze these sex-related differences in male and female Wistar rats (aged 26 days and 3, 7, and 14 months), and to assess their potential relationship with alterations in the capacity of adipose tissue expansion and the dysregulation of the main adipokines produced by the adipose tissue, leptin and adiponectin. Adiposity related parameters, blood parameters, the expression of genes related to expandability and inflammation (WAT), lipid metabolism (liver), and leptin and insulin signaling (both tissues) were measured. In females, adiposity index and WAT DNA content gradually increased with age, whereas males peaked at 7 months. A similar sex-dependent pattern was observed for leptin expression in WAT, while Mest expression levels decreased with age in males but not in females. Females also showed increased expression of the proliferation marker PCNA in the inguinal WAT compared to males. In males, leptin/adiponectin ratio greatly increased from 7 to 14 months in a more acute manner than in females, along with an increase in HOMA-IR index and hepatic triacylglyceride content, while no changes were observed in females. In liver, 14-month-old males displayed decreased mRNA levels of lnsr, Ampkor2, and Cptla compared with levels at 7 months. Males also showed decreased mRNA levels of Obrb (both tissues), and increased expression levels of Cd68 and Emrl (WAT) with age. In conclusion, females are more protected from age-related metabolic disturbances, such as insulin resistance, hepatic lipid deposition, and WAT inflammation compared to males. This may be related to their greater capacity for WAT expansion reflected by a greater Mest/leptin mRNA ratio and to their ability to maintain adiponectin levels and preserve leptin sensitivity with aging.en
dc.description.sponsorshipThis work was supported by the EU's 7th Framework Programme FP7 2007-2013, no. 244995 (BIOCLAIMS Project) and the Institute de Salud Carlos III, Centro de Investigacion Biomedica en Red Fisiopatologla de la Obesidad y Nutrition, CIBERohn. Authors belong to the Nutrigenomics-group at UIB, awarded as Group of Excellence of the Autonomous Community of the Balearic Islands (CAIB) and supported by Direccio General d'Universitats, Recerca i Transferencia del Coneixement of Regional Government (CAIB) and FEDER funds (EU). The Laboratory is a member of the European Research Network of Excellence NuGO (The European Nutrigenomics Organization, EU Contract: no. FP6-506360). NS is granted with a Ph.D. fellowship entitled beta para la formacion de personal investigador, co-funded by the Regional Government (Conselleria d'Educacio, Cultura i Universitats, CAIB) and the European Social Fund (FSE).es_ES
dc.language.isoengen
dc.publisherFrontiers Media en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSex-differences
dc.subjectWhite adipose tissue expandability
dc.subjectMetabolic disturbances
dc.subjectLeptin/adiponectin ratio
dc.subjectMEST
dc.titleSexual Dimorphism in the Age-Induced Insulin Resistance, Liver Steatosis, and Adipose Tissue Function in Ratsen
dc.typeresearch articleen
dc.rights.licenseAttribution 4.0 International*
dc.identifier.pubmedID28744221es_ES
dc.format.volume8es_ES
dc.format.page445es_ES
dc.identifier.doi10.3389/fphys.2017.00445
dc.relation.publisherversionhttps://dx.doi.org/10.3389/fphys.2017.00445en
dc.identifier.journalFrontiers in Physiologyes_ES
dc.rights.accessRightsopen accessen
dc.identifier.scopus2-s2.0-85025443590
dc.identifier.wos405170800001
dc.identifier.puiL617388159


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