IFEC   20925
INSTITUTO DE FARMACOLOGIA EXPERIMENTAL DE CORDOBA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Activation of Cannabinoid CB1 Receptor within Nucleus Accumbens Core Underlies Restraint Stress-Induced Reinstatement in Extinguished Cocaine?Conditioned Animal
Autor/es:
43. ANDREA SUSANA GUZMÁN, LAURA NOEMÍ DE GIOVANNI, MIRIAM BEATRIZ VIRGOLINI, LILIANA MARINA CANCELA.
Lugar:
Huerta Grande, Córdoba
Reunión:
Congreso; XXIX Reunión Annual. Sociedad Argentina de Neurociencias; 2014
Institución organizadora:
Sociedad Argentina de Investigación en Neurociencias
Resumen:
P118.-Activation of Cannabinoid CB1 Receptor within Nucleus Accumbens Core Underlies Restraint Stress-Induced Reinstatement in Extinguished Cocaine?Conditioned Animal Andrea Susana Guzmán1°, Laura Noemí De Giovanni1°, Miriam Beatriz Virgolini1°, Liliana Marina Cancela1° 1°IFEC ? CONICET; Departamento de Farmacología. FCQ. UNC andreasuguz@gmail.com Endocannabinoid system, primarily through their actions at CB1 receptor, is implicated in drug relapse. Moreover, the Nucleus Accumbens (NAc), a high density cannabinoid CB1 receptors brain region, is involved in cocaine and stress-induced reinstatement. Previous results from our lab demonstrated that in extinguished cocaine-conditioned animals evaluated in a conditioned place preference test (CPP), the restraint-stress reinstated the cocaine CPP and that phenomenon depends on the glutamatergic transmission within NAc. Additionally, in our lab it has been revealed that intra-Core administration of AM251, a CB1 antagonist, abrogated that restraint stress-induced reinstatement. According to the previous protocol, extinguished cocaine-conditioned Wistar rats were microinjected intra-Core with a CB1 agonist, ACEA, (0, 0.001 or 0.01 fmol/side) or vehicle, and subsequently assigned to the following treatments: 1) Stressed Animals (SA): 15 min-restraint exposure, a non-reinstatement session, and 2) Control Animals (CA). Intra-core ACEA administration facilitated the restraint stress-induced reinstatement in SA. Our results support the hypothesis of the influence of CB1 receptors in restraint stress-induced reinstatement. Future studies will focus on a possible glutamate dependent mechanism within NAc Core to explain the effect of CB1 receptor activation on restraint stress-induced reinstatement.