Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/4500
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dc.contributor.authorDakić, Tamaraen_US
dc.contributor.authorLakić, Ivaen_US
dc.contributor.authorZec, Manjaen_US
dc.contributor.authorTakic, Marijaen_US
dc.contributor.authorStojiljkovic, Mojcaen_US
dc.contributor.authorJevđović, Tanjaen_US
dc.date.accessioned2021-10-29T16:14:29Z-
dc.date.available2021-10-29T16:14:29Z-
dc.date.issued2021-11-01-
dc.identifier.issn0022-5142-
dc.identifier.issn1097-0010-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/4500-
dc.description.abstractBackground: Nutritional modulations may be considered a strategy to protect mental health. Neuronal homeostasis is highly dependent on the availability of glucose, which represents the primary energy source for the brain. In this study, we evaluated the effects of walnut intake and fructose-rich diet on the expression of glucose transporters (GLUTs) in two rat brain regions: hypothalamus and hippocampus. Results: Our results show that walnut supplementation of fructose-fed animals restored the hypothalamic content of GLUT1 and GLUT3 protein. Furthermore, walnut intake did not affect increased hypothalamic GLUT2 content upon fructose consumption. These effects were accompanied by distinctive alterations of hippocampal GLUTs levels. Specifically, walnut intake increased GLUT1 content, whereas GLUT2 protein was decreased within the rat hippocampus after both individual and combined treatments. Conclusion: Overall, our study suggests that walnut supplementation exerted modulatory effects on the glucose transporters within specific brain regions in the presence of developed metabolic disorder. © 2021 Society of Chemical Industry.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of the Science of Food and Agricultureen_US
dc.subjectfructoseen_US
dc.subjectglucose transportersen_US
dc.subjecthippocampusen_US
dc.subjecthypothalamusen_US
dc.subjectwalnuten_US
dc.titleFructose‐rich diet and walnut supplementation differently regulate rat hypothalamic and hippocampal glucose transporters expressionen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/jsfa.11252-
dc.description.rankM21en_US
dc.description.impact3,638en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Comparative Physiology and Ecophysiology-
crisitem.author.deptChair of Comparative Physiology and Ecophysiology-
crisitem.author.deptChair of Comparative Physiology and Ecophysiology-
crisitem.author.orcid0000-0002-7238-2728-
crisitem.author.orcid0000-0001-8894-7300-
crisitem.author.orcid0000-0001-6047-9365-
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