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dc.contributor.authorFlorensa Zanuy, Eva Ariadna es_ES
dc.contributor.authorGarro Martínez, Emilioes_ES
dc.contributor.authorAdell Calduch, Albertes_ES
dc.contributor.authorCastro Fernández, María Elena es_ES
dc.contributor.authorDíaz Martínez, Álvaro es_ES
dc.contributor.authorPazos Carro, Ángel es_ES
dc.contributor.authorMac-Dowell, Karina S.es_ES
dc.contributor.authorMartín-Hernández, Davides_ES
dc.contributor.authorPilar Cuéllar, María Fuencisla es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-04-04T16:00:38Z
dc.date.available2022-04-04T16:00:38Z
dc.date.issued2021-03es_ES
dc.identifier.issn0006-2952es_ES
dc.identifier.issn1873-2968es_ES
dc.identifier.otherSAF2015-67457-Res_ES
dc.identifier.urihttp://hdl.handle.net/10902/24495
dc.description.abstractMajor Depression is a severe psychiatric condition with a still poorly understood etiology. In the last years, evidence supporting the neuroinflammatory hypothesis of depression has increased. In the current clinical scenario, in which the available treatments for depression is far from optimal, there is an urgent need to develop fast-acting drugs with fewer side effects. In this regard, recent pieces of evidence suggest that cannabidiol (CBD), the major non-psychotropic component of Cannabis sativa with anti-inflammatory properties, appears as a drug with antidepressant properties. In this work, CBD 30 mg/kg was administered systemically to mice 30 min before lipopolysaccharide (LPS; 0.83 mg/kg) administration as a neuroinflammatory model, and behavioral tests for depressive-, anhedonic- and anxious-like behavior were performed. NF-?B, I?B? and PPAR? levels were analyzed by western blot in nuclear and cytosolic fractions of cortical samples. IL-6 and TNF? levels were determined in plasma and prefrontal cortex using ELISA and qPCR techniques, respectively. The precursor tryptophan (TRP), and its metabolites kynurenine (KYN) and serotonin (5-HT) were measured in hippocampus and cortex by HPLC. The ratios KYN/TRP and KYN/5-HT were used to estimate indoleamine 2,3-dioxygenase (IDO) activity and the balance of both metabolic pathways, respectively. CBD reduced the immobility time in the tail suspension test and increased sucrose preference in the LPS model, without affecting locomotion and central activity in the open-field test. CBD diminished cortical NF-?B activation, IL-6 levels in plasma and brain, and the increased KYN/TRP and KYN/5-HT ratios in hippocampus and cortex in the LPS model. Our results demonstrate that CBD produced antidepressant-like effects in the LPS neuroinflammatory model, associated to a reduction in the kynurenine pathway activation, IL-6 levels and NF-?B activation. As CBD stands out as a promising antidepressant drug, more research is needed to completely understand its mechanisms of action in depression linked to inflammation.es_ES
dc.description.sponsorshipFUNDING AND ACKNOWLEDGMENTS: This research was supported by the Ministerio de Economía y Competitividad (SAF2015-67457-R MINECO/FEDER), the Ministerio de Ciencia, Innovación y Universidades (RTI2018-097534-B-I00), the Instituto de Salud Carlos III (PI19/00170), and Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM). E F-Z was supported by a predoctoral fellowship from the Universidad de Cantabria (Spain). We acknowledge the technical assistance of Annamaria Architravo and Deborah Vasturzo, and Dr Rebeca Vidal for her scientific advice.es_ES
dc.format.extent11 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights© 2021. This manuscript version is made available under the CC-BY-NC-ND 4.0 license*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceBiochem Pharmacol . 2021 Mar;185:114433es_ES
dc.subject.othercannabidioles_ES
dc.subject.otherantidepressantes_ES
dc.subject.otherantidepressantes_ES
dc.subject.otherkynureninees_ES
dc.subject.otherIL-6es_ES
dc.subject.otherNF-ĸBes_ES
dc.titleCannabidiol antidepressant-like effect in the lipopolysaccharide model in mice: Modulation of inflammatory pathwayses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.bcp.2021.114433es_ES
dc.identifier.DOI10.1016/j.bcp.2021.114433es_ES
dc.type.versionacceptedVersiones_ES


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Attribution-NonCommercial-NoDerivatives 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 International