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dc.contributor.authorPeñasco Iglesias, Sara
dc.contributor.authorRico Barrio, Irantzu
dc.contributor.authorPuente Bustinza, Nagore ORCID
dc.contributor.authorGómez Urquijo, Sonia María ORCID
dc.contributor.authorFontaine, Christine J.
dc.contributor.authorEgaña Huguet, Jon
dc.contributor.authorAchicallende Urcaregui, Svein ORCID
dc.contributor.authorRamos Uriarte, Almudena ORCID
dc.contributor.authorReguero Acebal, Leire ORCID
dc.contributor.authorElezgarai Gabantxo, Izaskun ORCID
dc.contributor.authorNahirney, Patrick C.
dc.contributor.authorChristie, Brian R.
dc.contributor.authorGrandes Moreno, Pedro Rolando ORCID
dc.date.accessioned2020-02-25T09:15:33Z
dc.date.available2020-02-25T09:15:33Z
dc.date.issued2019-04-22
dc.identifier.citationNeuropharmacology 153 : 32-40 (2019)es_ES
dc.identifier.issn0028-3908
dc.identifier.issn1873-7064
dc.identifier.urihttp://hdl.handle.net/10810/41425
dc.description.abstractThe endocannabinoid system modulates synaptic plasticity in the hippocampus, but a link between long-term synaptic plasticity and the type 1 cannabinoid (CB1) receptor at medial perforant path (MPP) synapses remains elusive. Here, immuno-electron microscopy in adult mice showed that similar to 26% of the excitatory synaptic terminals in the middle 1/3 of the dentate molecular layer (DML) contained CB1 receptors, and field excitatory postsynaptic potentials evoked by MPP stimulation were inhibited by CB1 receptor activation. In addition, MPP stimulation at 10 Hz for 10 min triggered CB, receptor-dependent excitatory long-term depression (eCB-eLTD) at MPP synapses of wild-type mice but not on CB1-knockout mice. This eCB-eLTD was group I mGluR-dependent, required intracellular calcium influx and 2-arachydonoyl-glycerol (2-AG) synthesis but did not depend on N-methyl-d-aspartate (NMDA) receptors. Overall, these results point to a functional role for CB1 receptors with eCB-eLTD at DML MPP synapses and further involve these receptors in memory processing within the adult brain.es_ES
dc.description.sponsorshipWe thank all members of P. Grandes laboratory for their helpful comments, suggestions, and discussions during the performance of this study. The authors thank Giovanni Marsicano (INSERM, U1215 Neurocentre Magendie, Endocannabinoids and Neuroadaptation, Bordeaux, France. University de Bordeaux, France), Beat Lutz (Institute of Physiological Chemistry and German Resilience Center, University Medical Center of the Johannes Gutenberg University Mainz, Germany) and Susana Mato (Achucarro Basque Center for Neuroscience, Science Park of the UPV/EHU, Leioa, Vizcaya, Spain) for providing the CB<INF>1</INF> receptor knock-out mice. This work was supported by MINECO/FEDER, UE (grant number SAF2015-65034-R to PG); The Basque Government (grant number BCG IT764-13 to PG); Red de Trastornos Adictivos, Instituto de Salud Carlos III (ISC-III) and European Regional Development Funds-European Union (ERDF-EU; grant RD16/0017/0012 to PG); PhD contract from MINECO (BES-2013-065057 to SP); Vanier Canada Graduate Scholarship (NSERC to CJF).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2015-65034-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/BES-2013-065057es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectcbes_ES
dc.subjectreceptores_ES
dc.subject2-ages_ES
dc.subjectelectrophysiologyes_ES
dc.subjectexcitatory synapseses_ES
dc.subjectlong-term depressiones_ES
dc.subjecthippocampuses_ES
dc.subjectcannabinoid receptores_ES
dc.subjectplasticityes_ES
dc.subjectsystemes_ES
dc.subjectactivationes_ES
dc.subjectmemoryes_ES
dc.subjectnmdaes_ES
dc.subjectcb1es_ES
dc.subjectinhibitiones_ES
dc.subjectobjectes_ES
dc.titleEndocannabinoid long-term depression revealed at medial perforant path excitatory synapses in the dentate gyruses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2019 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0028390819301364?via%3Dihubes_ES
dc.identifier.doi10.1016/j.neuropharm.2019.04.020
dc.departamentoesNeurocienciases_ES
dc.departamentoeuNeurozientziakes_ES


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© 2019 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).
Except where otherwise noted, this item's license is described as © 2019 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).