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CB1 and CB2 receptors in the bed nucleus of the stria terminalis differently modulate anxiety-like behaviors in rats

dc.contributor.authorGomes-de-Souza, Lucas [UNESP]
dc.contributor.authorBianchi, Paula C.
dc.contributor.authorCosta-Ferreira, Willian [UNESP]
dc.contributor.authorTomeo, Rodrigo A. [UNESP]
dc.contributor.authorCruz, Fábio C.
dc.contributor.authorCrestani, Carlos C. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionSão Paulo Federal University
dc.date.accessioned2021-06-25T10:23:09Z
dc.date.available2021-06-25T10:23:09Z
dc.date.issued2021-08-30
dc.description.abstractThe endocannabinoid system is implicated in anxiety, but the brain sites involved are not completely understood. The bed nucleus of the stria terminalis (BNST) has been related to anxiety and responses to aversive threats. Besides, endocannabinoid neurotransmission acting via CB1 receptors was identified in the BNST. However, the presence of CB2 receptors and the role of BNST endocannabinoid system in anxiety-like behaviors have never been reported. Therefore, this study investigated the presence of CB1 and CB2 receptors in the BNST and their role in anxiety-like behaviors. For this, gene expression of the endocannabinoid receptors was evaluated in samples from anterior and posterior BNST. Besides, behaviors were evaluated in the elevated plus-maze (EPM) in unstressed rats (trait anxiety-like behavior) and after exposure to restraint stress (restraint-evoked anxiety-like behavior) in rats treated with either the CB1 receptor antagonist AM251 or the CB2 receptor antagonist JTE907 into the anterior BNST. The presence of CB1 and CB2 receptors gene expression was identified in anterior and posterior divisions of the BNST. Bilateral microinjection of AM251 into the anterior BNST dose-dependently increased EPM open arms exploration in unstressed animals and inhibited the anxiety-like behavior in the EPM evoked by restraint. Conversely, intra-BNST microinjection of JTE907 decreased EPM open arms exploration in a dose-dependent manner and inhibited restraint-evoked behavioral changes in the EPM. Taken together, these results indicate that CB1 and CB2 receptors present in the BNST are involved in control of anxiety-like behaviors, and control by the latter is affected by previous stress experience.en
dc.description.affiliationLaboratory of Pharmacology School of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationJoint UFSCar-UNESP Graduate Program in Physiological Sciences
dc.description.affiliationDepartment of Pharmacology Paulista Medicine School São Paulo Federal University
dc.description.affiliationUnespLaboratory of Pharmacology School of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespJoint UFSCar-UNESP Graduate Program in Physiological Sciences
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2017/19249-0
dc.identifierhttp://dx.doi.org/10.1016/j.pnpbp.2021.110284
dc.identifier.citationProgress in Neuro-Psychopharmacology and Biological Psychiatry, v. 110.
dc.identifier.doi10.1016/j.pnpbp.2021.110284
dc.identifier.issn1878-4216
dc.identifier.issn0278-5846
dc.identifier.scopus2-s2.0-85101100155
dc.identifier.urihttp://hdl.handle.net/11449/205903
dc.language.isoeng
dc.relation.ispartofProgress in Neuro-Psychopharmacology and Biological Psychiatry
dc.sourceScopus
dc.subjectBNST
dc.subjectElevated plus maze
dc.subjectEndocannabinoid
dc.subjectGene expression
dc.subjectRestraint stress
dc.titleCB1 and CB2 receptors in the bed nucleus of the stria terminalis differently modulate anxiety-like behaviors in ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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