Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/32923

TitleDifferential and converging molecular mechanisms of antidepressants' action in the hippocampal dentate gyrus
Author(s)Patrício, P.
Pinheiro, António Mateus
Irmler, Martin
Alves, Nuno D.
Santos, Ana R. Machado
Morais, Mónica
Silva-Correia, Joana
Korostynski, Michal
Piechota, Marcin
Stoffel, Rainer
Beckers, Johannes
Bessa, J. M.
Almeida, O. F. X.
Sousa, Nuno
Pinto, Luísa
Issue date2015
PublisherPalgrave Macmillan
JournalNeuropsychopharmacology
CitationPatricio, P., Mateus-Pinheiro, A., Irmler, M., Alves, N. D., Machado-Santos, A. R., Morais, M., . . . Pinto, L. (2015). Differential and Converging Molecular Mechanisms of Antidepressants' Action in the Hippocampal Dentate Gyrus. Neuropsychopharmacology, 40(2), 338-349. doi: 10.1038/npp.2014.176
Abstract(s)Major depression is a highly prevalent, multidimensional disorder. Although several classes of antidepressants (ADs) are currently available, treatment efficacy is limited, and relapse rates are high; thus, there is a need to find better therapeutic strategies. Neuroplastic changes in brain regions such as the hippocampal dentate gyrus (DG) accompany depression and its amelioration with ADs. In this study, the unpredictable chronic mild stress (uCMS) rat model of depression was used to determine the molecular mediators of chronic stress and the targets of four ADs with different pharmacological profiles (fluoxetine, imipramine, tianeptine, and agomelatine) in the hippocampal DG. All ADs, except agomelatine, reversed the depression-like behavior and neuroplastic changes produced by uCMS. Chronic stress induced significant molecular changes that were generally reversed by fluoxetine, imipramine, and tianeptine. Fluoxetine primarily acted on neurons to reduce the expression of pro-inflammatory response genes and increased a set of genes involved in cell metabolism. Similarities were found between the molecular actions and targets of imipramine and tianeptine that activated pathways related to cellular protection. Agomelatine presented a unique profile, with pronounced effects on genes related to Rho-GTPase-related pathways in oligodendrocytes and neurons. These differential molecular signatures of ADs studied contribute to our understanding of the processes implicated in the onset and treatment of depression-like symptoms.
TypeArticle
URIhttp://hdl.handle.net/1822/32923
DOI10.1038/npp.2014.176
ISSN0893-133X
Publisher versionhttp://www.nature.com
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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