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Endocannabinoid neuromodulation in the neostriatum decreases the GABAergic striato-nigral disinhibitory function and increases the nigro-collicular inhibitory pathway activity

dc.contributor.authorda Silva, Juliana Almeida
dc.contributor.authorAlmada, Rafael Carvalho [UNESP]
dc.contributor.authorde Paiva, Yara Bezerra
dc.contributor.authorCoimbra, Norberto Cysne
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionBehavioural Neurosciences Institute (INeC)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T02:24:59Z
dc.date.available2020-12-12T02:24:59Z
dc.date.issued2020-08-01
dc.description.abstractWe previously reported the involvement of neostriato-nigral projections in the organisation of innate fear and panic attack-like responses organised by dorsal midbrain neurons, such as the periaqueductal grey matter and the deep layers of the superior colliculus (dlSC). In addition, several lines of evidence have demonstrated that cannabinoid receptor type 1 is found in the neostriatum (caudate nucleus and putamen; CPu). In the present study, we investigated the role of endocannabinoid neuromodulation in CPu in the expression of unconditioned fear-related behavioural responses elicited by microinjections of the γ-aminobutyric acid (GABA)A receptor selective antagonist bicuculline (BIC) in the dlSC. Wistar rats received injection of vehicle or anandamide (AEA) at 0.5, 5, 50, 100 pmol in CPu, followed by injections of BIC in a dose of 40 ng in the dlSC. The treatment of the CPu with AEA in a dose of 5 and 50 pmol attenuated the unconditioned fear-related behaviour, such as defensive alertness, defensive immobility and escape, induced by GABAA receptor blockade in dlSC. These findings suggest that endogenous cannabinoids acting on CPu neurons exert an indirect modulatory influence on the activity of superior colliculus neurons, possibly through an inhibitory activity on neostriato-nigral disinhibitory connections that modulate the nigro-collicular inhibitory GABAergic pathways.en
dc.description.affiliationLaboratório de Neuroanatomia and Neuropsicobiologia Departamento de Farmacologia Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FMRP-USP), Av. Bandeirantes, 3900
dc.description.affiliationBehavioural Neurosciences Institute (INeC), Av. do Café, 2450, Monte Alegre
dc.description.affiliationDepartment of Biological Sciences School of Sciences Humanities and Languages São Paulo State University (UNESP)
dc.description.affiliationNAP-USP-Neurobiology of Emotions Research Centre (NuPNE) Ribeirão Preto Medical School University of São Paulo (FMRP-USP), Av. Bandeirantes, 3900
dc.description.affiliationUnespDepartment of Biological Sciences School of Sciences Humanities and Languages São Paulo State University (UNESP)
dc.format.extent1199-1208
dc.identifierhttp://dx.doi.org/10.1007/s00702-020-02217-8
dc.identifier.citationJournal of Neural Transmission, v. 127, n. 8, p. 1199-1208, 2020.
dc.identifier.doi10.1007/s00702-020-02217-8
dc.identifier.issn1435-1463
dc.identifier.issn0300-9564
dc.identifier.scopus2-s2.0-85086321603
dc.identifier.urihttp://hdl.handle.net/11449/201137
dc.language.isoeng
dc.relation.ispartofJournal of Neural Transmission
dc.sourceScopus
dc.subjectAnandamide
dc.subjectCaudate nucleus
dc.subjectDeep layers of superior colliculus
dc.subjectPutamen
dc.subjectStriatonigral-nigrotectal GABAergic pathways
dc.subjectUnconditioned fear
dc.titleEndocannabinoid neuromodulation in the neostriatum decreases the GABAergic striato-nigral disinhibitory function and increases the nigro-collicular inhibitory pathway activityen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-4676-2620[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentNeurologia, Psicologia e Psiquiatria - FMBpt

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