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Lycopene in Combination with Insulin Triggers Antioxidant Defenses and Increases the Expression of Components That Detoxify Advanced Glycation Products in Kidneys of Diabetic Rats

dc.contributor.authorFigueiredo, Ingrid Delbone [UNESP]
dc.contributor.authorLima, Tayra Ferreira Oliveira [UNESP]
dc.contributor.authorCarlstrom, Paulo Fernando [UNESP]
dc.contributor.authorAssis, Renata Pires [UNESP]
dc.contributor.authorBrunetti, Iguatemy Lourenço [UNESP]
dc.contributor.authorBaviera, Amanda Martins [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionPaulista University (Unip)
dc.date.accessioned2025-04-29T18:41:59Z
dc.date.issued2024-05-23
dc.description.abstractBACKGROUND: Biochemical events provoked by oxidative stress and advanced glycation may be inhibited by combining natural bioactives with classic therapeutic agents, which arise as strategies to mitigate diabetic complications. The aim of this study was to investigate whether lycopene combined with a reduced insulin dose is able to control glycemia and to oppose glycoxidative stress in kidneys of diabetic rats. METHODS: Streptozotocin-induced diabetic rats were treated with 45 mg/kg lycopene + 1 U/day insulin for 30 days. The study assessed glycemia, insulin sensitivity, lipid profile and paraoxonase 1 (PON-1) activity in plasma. Superoxide dismutase (SOD) and catalase (CAT) activities and the protein levels of advanced glycation end-product receptor 1 (AGE-R1) and glyoxalase-1 (GLO-1) in the kidneys were also investigated. RESULTS: An effective glycemic control was achieved with lycopene plus insulin, which may be attributed to improvements in insulin sensitivity. The combined therapy decreased the dyslipidemia and increased the PON-1 activity. In the kidneys, lycopene plus insulin increased the activities of SOD and CAT and the levels of AGE-R1 and GLO-1, which may be contributing to the antialbuminuric effect. CONCLUSIONS: These findings demonstrate that lycopene may aggregate favorable effects to insulin against diabetic complications resulting from glycoxidative stress.en
dc.description.affiliationDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University (Unesp)
dc.description.affiliationInstitute of Health Sciences Paulista University (Unip)
dc.description.affiliationUnespDepartment of Clinical Analysis School of Pharmaceutical Sciences São Paulo State University (Unesp)
dc.identifierhttp://dx.doi.org/10.3390/nu16111580
dc.identifier.citationNutrients, v. 16, n. 11, 2024.
dc.identifier.dimensionspub.1172038499
dc.identifier.doi10.3390/nu16111580
dc.identifier.issn2072-6643
dc.identifier.orcid0000-0003-0987-5295
dc.identifier.orcid0000-0002-2218-3616
dc.identifier.orcid0000-0003-1558-2894
dc.identifier.orcid0000-0003-4927-7599
dc.identifier.orcid0000-0003-1408-2724
dc.identifier.pmcidPMC11173891
dc.identifier.pmid38892513
dc.identifier.scopus2-s2.0-85196611363
dc.identifier.urihttps://hdl.handle.net/11449/299300
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofNutrients
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceScopus
dc.sourceDimensions
dc.subjectantidiabetic activity
dc.subjectdiabetic complications
dc.subjectglycoxidative stress
dc.subjectglyoxalase
dc.subjectnatural bioactives
dc.subjectparaoxonase
dc.titleLycopene in Combination with Insulin Triggers Antioxidant Defenses and Increases the Expression of Components That Detoxify Advanced Glycation Products in Kidneys of Diabetic Ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0002-2218-3616[3]
unesp.author.orcid0000-0003-0987-5295[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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