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Delta9-tetrahydrocannabinol decreases somatic and motivational manifestations of nicotine withdrawal in mice

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dc.contributor.author Aso Pérez, Ester
dc.contributor.author Maldonado, Rafael, 1961-
dc.contributor.author Murtra, Patricia
dc.contributor.author Balerio, Graciela N.
dc.contributor.author Berrendero Díaz, Fernando, 1971-
dc.date.accessioned 2011-07-27T08:27:41Z
dc.date.available 2011-07-27T08:27:41Z
dc.date.issued 2004
dc.identifier.citation Balerio GN, Aso E, Berrendero F, Murtra P, Maldonado R. Δ9-tetrahydrocannabinol decreases somatic and motivational manifestations of nicotine withdrawal in mice. Eur J Neurosci. 2004;20:2737-48. DOI: 10.1111/j.1460-9568.2004.03714.x
dc.identifier.issn 0953-816X
dc.identifier.uri http://hdl.handle.net/10230/12416
dc.description.abstract The possible interactions between Delta9-tetrahydrocannabinol (THC) and nicotine remain unclear in spite of the current association of cannabis and tobacco in humans. The aim of the present study was to explore the interactions between these two drugs of abuse by evaluating the consequences of THC administration on the somatic manifestations and the aversive motivational state associated to nicotine withdrawal in mice. Acute THC administration significantly decreased the incidence of several nicotine withdrawal signs precipitated by mecamylamine or naloxone, such as wet-dog-shakes, paw tremor and scratches. In both experimental conditions, the global withdrawal score was also significantly attenuated by acute THC administration. THC also reversed conditioned place aversion associated to naloxone precipitated nicotine withdrawal. We have then evaluated whether this effect of THC was due to possible adaptive changes induced by chronic nicotine on CB1 cannabinoid receptors. The stimulation of GTPS-binding proteins by the cannabinoid agonist WIN 55,212-2 and the density of CB1 cannabinoid receptor binding labelled with [3H] CP-55,940 were not modified by chronic nicotine treatment in the different brain structures investigated. Finally, we evaluated the consequences of THC administration on c-Fos expression in several brain structures after chronic nicotine administration and withdrawal. c-Fos was decreased in the caudate putamen and the dentate gyrus after mecamylamine precipitated nicotine withdrawal. However, acute THC administration did not modify c-Fos expression under these experimental conditions. Taken together, these results indicate that THC administration attenuated somatic signs of nicotine withdrawal and this effect was not associated to compensatory changes on CB1 cannabinoid receptors during chronic nicotine administration. In addition, THC also ameliorated the aversive motivational consequences of nicotine withdrawal.
dc.description.sponsorship This work has been supported by grants from Human Frontier Science Program Organization (RG0077/2000-B), Plan Nacional sobre Drogas, Generalitat de Catalunya (Research Distinction), 2002 SGR00193 and the European Comission “Quality of Life and Management of Living Resources QLRT-2001-01691. Graciela Balerio is a postdoctoral fellow supported by “Fundación Carolina”. Fernando Berrendero is a researcher supported by “Ramón y Cajal” research program of the Ministery of Science and Technology.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Wiley-Blackwell
dc.relation.ispartof European Journal of Neuroscience. 2004;20:2737-48
dc.rights © 2004 Federation of European Neuroscience Societies
dc.subject.other Cannabinoides -- Efectes fisiològics
dc.subject.other Nicotina -- Receptors
dc.subject.other Cannabinoides -- Receptors
dc.subject.other Nicotina -- Efectes fisiològics
dc.title Delta9-tetrahydrocannabinol decreases somatic and motivational manifestations of nicotine withdrawal in mice
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1111/j.1460-9568.2004.03714.x
dc.subject.keyword THC
dc.subject.keyword Nicotine withdrawal
dc.subject.keyword Place aversion
dc.subject.keyword Cannabinoid receptor
dc.subject.keyword c-Fos
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/submittedVersion

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