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dc.contributor.authorViudez-Martínez, Adriánes_ES
dc.contributor.authorGarcía-Gutiérrez, María Saludes_ES
dc.contributor.authorMedrano-Relinque, Juanes_ES
dc.contributor.authorNavarrón, Carmen M.es_ES
dc.contributor.authorNavarrete, Franciscoes_ES
dc.contributor.authorManzanares, Jorgees_ES
dc.date.accessioned2020-08-11T07:06:04Z-
dc.date.available2020-08-11T07:06:04Z-
dc.date.issued2019-
dc.identifier.citationActa Pharmacologica Sinica 40: 358–364 (2019)es_ES
dc.identifier.issn1671-4083-
dc.identifier.urihttp://hdl.handle.net/10261/217697-
dc.description.abstractRecent evidence suggests that cannabidiol (CBD) may be useful for the treatment of different neuropsychiatric disorders. However, some controversy regarding its profile as a drug of abuse hampers the further development of basic and clinical studies. In this study, the behavioral profile of CBD as a potential drug of abuse was evaluated in C57BL/6J mice. Reinforcing properties of CBD (15, 30, and 60 mg/kg; i.p.) were assessed using the conditioned place preference (CPP) paradigm. Spontaneous withdrawal symptoms and motor activity in the open field were examined 12 h after the last CBD administration (30 mg/kg/12 h, i.p., 6 days). CBD plasma concentrations were measured at 2, 4, 8, 12, and 24 h after the administration of CBD (30 mg/kg, i.p.). Furthermore, an oral CBD self-administration paradigm (50 mg/kg; CBD water-soluble 1.2 mg/mL) was performed to evaluate whether this drug produced any effects on motivation compared with a non-reinforcing substance (water). We found that CBD failed to induce CPP, withdrawal symptoms, or altered motor behavior 12 h after its administration. At that time, only traces of CBD were detected, ensuring that the lack of alterations in somatic signs and locomotor activity was not due to residual drug in plasma. Interestingly, mice displayed similar motivation and consumption of CBD and water. Taken together, these results show that CBD lacks activity as a drug of abuse and should stimulate the development of the basic and clinical studies needed to elucidate its potential therapeutic use for the treatment of neuropsychiatric and drug use disorders.es_ES
dc.description.sponsorshipThis work was supported by the “Instituto de Salud Carlos III” (RETICS, RD12/0028/0019), “Plan Nacional Sobre Drogas” (PNSD 2016/016), and “Ministerio de Economía y Competitividad” (FIS, PI14/00438) to JM. AVM is a predoctoral fellow supported by “Plan Nacional Sobre Drogas” (PNSD 2016/016).es_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.rightsclosedAccesses_ES
dc.titleCannabidiol does not display drug abuse potential in mice behaviores_ES
dc.typeartículoes_ES
dc.identifier.doi10.1038/s41401-018-0032-8-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41401-018-0032-8es_ES
dc.identifier.e-issn1745-7254-
dc.contributor.funderMinisterio de Economía y Competitividad (España)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
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