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AdipoRon as a Novel Therapeutic Agent for Depression: A Comprehensive Review of Preclinical Evidence

dc.contributor.authorLaurindo, Lucas Fornari
dc.contributor.authorRodrigues, Victória Dogani
dc.contributor.authorMellen, Rodrigo Haber
dc.contributor.authorde Argollo Haber, Rafael Santos
dc.contributor.authorValenti, Vitor Engrácia [UNESP]
dc.contributor.authorLaurindo, Lívia Fornari
dc.contributor.authorChagas, Eduardo Federighi Baisi
dc.contributor.authorde Oliveira, Camila Marcondes
dc.contributor.authorDireito, Rosa
dc.contributor.authorMiglino, Maria Angélica
dc.contributor.authorBarbalho, Sandra Maria
dc.date.accessioned2026-04-27T12:18:22Z
dc.date.issued2025-07-31
dc.description.abstractBackground/Objectives: Depression is a mood disorder that causes persistent sadness and loss of interest, and its etiology involves a condition known as hypoadiponectinemia, which is prevalent in depressive individuals compared with healthy individuals and causes neuroinflammation. The use of intact adiponectin protein to target neuroinflammation in depressive moods is complex due to the difficulties associated with using the intact protein. AdipoRon, a synthetic oral adiponectin receptor agonist that targets the AdipoR1 and AdipoR2 receptors for adiponectin, has emerged in this context. Its most prominent effects include reduced inflammation and the attenuation of oxidative stress. To the best of our knowledge, no comprehensive review has addressed these results so far. To fill this literature gap, we present a comprehensive review examining the effectiveness of AdipoRon in treating depression. Methods: Only preclinical models are included due to the absence of clinical studies. Results: Analyzing the included studies shows that AdipoRon demonstrates contrasting effects against depression. However, most of the evidence underscores AdipoRon-based adiponectin replacement therapies as potential candidates for future treatment against this critical psychiatric condition due to their anti-neuroinflammatory potential, ultimately inhibiting several neuroinflammatory pathways. Conclusions: Future research endeavors must address several limitations due to the heterogeneity of the studies' methodologies and results.en
dc.description.affiliationPostgraduate Program in Structural and Functional Interactions in Rehabilitation, School of Medicine, Universidade de Marília (UNIMAR), Marília 17525-902, São Paulo, Brazil
dc.description.affiliationDepartment of Biochemistry and Pharmacology, School of Medicine, Universidade de Marília (UNIMAR), Marília 17525-902, São Paulo, Brazil
dc.description.affiliationDepartment of Biochemistry and Pharmacology, School of Medicine, Faculdade de Medicina de Marília (FAMEMA), Marília 17519-030, São Paulo, Brazil
dc.description.affiliationAutonomic Nervous System Center, School of Philosophy and Sciences, São Paulo State University, Marília 17525-902, São Paulo, Brazil
dc.description.affiliationDepartment of Biochemistry and Pharmacology, School of Medicine, Faculdade de Medicina de São José do Rio Preto (FAMERP), São José do Rio Preto 15090-000, São Paulo, Brazil
dc.description.affiliationLaboratory of Systems Integration Pharmacology, Clinical and Regulatory Science, Research Institute for Medicines, Universidade de Lisboa (iMed.ULisboa), Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal
dc.description.affiliationDepartment of Biochemistry and Nutrition, School of Food and Technology of Marília (FATEC), Marília 17500-000, São Paulo, Brazil
dc.description.affiliationDepartment of Research, Research Coordination Center, UNIMAR Charitable Hospital, Universidade de Marília (UNIMAR), Marília 17525-902, São Paulo, Brazil
dc.description.affiliationUnespAutonomic Nervous System Center, School of Philosophy and Sciences, São Paulo State University, Marília 17525-902, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1191400222
dc.identifier.dimensionspub.1191400222
dc.identifier.doi10.3390/biomedicines13081867
dc.identifier.issn2227-9059
dc.identifier.orcid0000-0003-3159-0982
dc.identifier.orcid0000-0001-7477-3805
dc.identifier.orcid0000-0003-4715-6160
dc.identifier.orcid0000-0002-4143-4302
dc.identifier.orcid0000-0003-4979-115X
dc.identifier.orcid0000-0002-5035-876X
dc.identifier.pmcidPMC12383995
dc.identifier.pmid40868122
dc.identifier.urihttps://hdl.handle.net/11449/322677
dc.publisherMDPI
dc.relation.ispartofBiomedicines; n. 8; v. 13; p. 1867
dc.rights.accessRightsAcesso abertopt
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dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleAdipoRon as a Novel Therapeutic Agent for Depression: A Comprehensive Review of Preclinical Evidence
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicatione22ddca4-2c85-4153-8a3a-3aae2af14eaa
relation.isOrgUnitOfPublication.latestForDiscoverye22ddca4-2c85-4153-8a3a-3aae2af14eaa
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Filosofia e Ciências, Maríliapt

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