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.