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dc.contributor.authorPopovic, Miroljub-
dc.contributor.authorCaballero Bleda, María-
dc.contributor.authorBenavente-García, Obdulio-
dc.contributor.authorCastillo, Julián-
dc.contributor.otherResearch Institute of Aging, University of Murcia,es
dc.contributor.otherResearch & Development Department of Nutrafur S.A., Alcantarilla (Murcia),es
dc.contributor.otherFacultades, Departamentos, Servicios y Escuelas::Departamentos de la UMU::Anatomía Humana y Psicobiología-
dc.date.accessioned2024-06-19T08:12:54Z-
dc.date.available2024-06-19T08:12:54Z-
dc.date.issued2013-11-27-
dc.identifier.citationJournal of Psychopharmacology, 2014, Vol. 28, N. 5, pp. 498-501.es
dc.identifier.issnPrint: 0269-8811-
dc.identifier.issnElectronic: 1461-7285-
dc.identifier.urihttp://hdl.handle.net/10201/142423-
dc.description© The Author(s) 2013. © 2014 SAGE Publications. This document is the Published version of a Published Work that appeared in final form in Journal of Psychopharmacology. To access the final edited and published work see https://doi.org/10.1177/0269881113512040-
dc.description.abstractThe present experiments were performed to study the effect of the flavonoid apigenin (20 mg/kg intraperitoneally (i.p.), 1 h before acquisition), on 24 h retention performance and forgetting of a step-through passive avoidance task, in young male Wistar rats. There were no differences between saline- and apigenin-treated groups in the 24 h retention trial. Furthermore, apigenin did not prevent the amnesia induced by scopolamine (1mg/kg, i.p., 30 min before the acquisition). The saline- and apigenin-treated rats that did not step through into the dark compartment during the cut-off time (540 s) were retested weekly for up to eight weeks. In the saline treated group, the first significant decline in passive avoidance response was observed at four weeks, and complete memory loss was found five weeks after the acquisition of the passive avoidance task. At the end of the experimental period, 60% of the animals treated with apigenin still did not step through. These data suggest that 1) apigenin delays the long-term forgetting but did not modulate the 24 h retention of fear memory and 2) the obtained beneficial effect of apigenin on the passive avoidance conditioning is mediated by mechanisms that do not implicate its action on the muscarinic cholinergic system.es
dc.formatapplication/pdfes
dc.format.extent4es
dc.languageenges
dc.publisherSAGE Publicationses
dc.relationThis work was supported by Nutrafur S.A. and the Spanish Centre for the Development of Industrial Technology (CDTI), as part of a SENIFOOD project, which belongs to the CENIT subvention program.es
dc.rightsinfo:eu-repo/semantics/embargoedAccesses
dc.subjectApigenines
dc.subjectFlavonoidses
dc.subjectMemory retentiones
dc.subjectForgettinges
dc.subjectPassive avoidancees
dc.subjectScopolaminees
dc.subject.otherCDU::6 - Ciencias aplicadases
dc.titleThe flavonoid apigenin delays forgetting of passive avoidance conditioning in ratses
dc.typeinfo:eu-repo/semantics/articlees
dc.relation.publisherversionhttps://journals.sagepub.com/doi/abs/10.1177/0269881113512040es
dc.embargo.termsSI-
dc.identifier.doihttps://doi.org/10.1177/0269881113512040-
Aparece en las colecciones:Artículos: Anatomía Humana y Psicobiología

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