IBCN   20355
INSTITUTO DE BIOLOGIA CELULAR Y NEUROCIENCIA "PROFESOR EDUARDO DE ROBERTIS"
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Deficiency of CB1 receptor produces alterations in dendritic fibers in striatum
Autor/es:
SORIANO, DELIA; CALTANA, LAURA ROMINA; MADARNAS, CATALINA; BRUSCO, ALICIA; NOVAK, LUCIANA; VILLALBA, NERINA
Lugar:
CABA
Reunión:
Congreso; IV International Congres in Translational Medicine; 2018
Institución organizadora:
IMBS-Universidad de Buenos Aires- Universidad de Freiburg
Resumen:
INTRODUCTION:The cannabinoid receptor type 1 (CB1R) is one of the most abundant G protein-coupled receptors in the central nervous system and is presynaptically located in axonal terminals, dendrites and soma. It is widely distributed in the Central Nervous System, both in neurons and glial cells and has a greater expression in areas such as hippocampus, cerebellum, cerebral cortex, striatum, among others.CB1R is involved in physiological processes such as memory, learning, motor coordination, anxiety and mood.Previous results of our group showed that hippocampal neurons presented less dendritic and axonal arborization and changes in the synaptic structure. AIMS: The aim of this work is to evaluate the axonal and dendritic neuronal cytoskeleton in the Striatum in the absence of CB1R, using cnr1 - / - knockout mice (CB1R - / -). EXPERIMENTAL PROCEDURE: Sixty-day-old female and male, CD1 CB1R wild type (CB1R+/+) and CB1R knock-out mice (CB1R-/-) were used in this study. CB1R-/- mice were generated by disruption of the cnr1 gene. Animals were fixed by intracardiac perfusion with 4% (w/v) parafolmaldehyde in 0.1M phosphate buffer (PB) pH 7.4 and post-fixed for 4h in the same solution. Coronal sections of the brains were cut with a vibratome (40µm thick) and stored in 50% (v/v) glycerol solution at -20°C until use. Immunohistochemistry was performed with primary antibodies: mouse anti-Syn (1:1000); mouse anti-MAP-2 (1:1000); mouse anti- NF160 (1:1000); mouse anti- NF200 (1:1000). In order to evaluate MAP-2, NF160+ and NF200+ fibers, the total area of the immunolabeled fibers was related to the total area of the corresponding microscopic field (20x primary magnification), rendering a relative area parameter. The intensity of Syn immunoreactivity was evaluated by means of a relative optical density (ROD).