ININFA   02677
INSTITUTO DE INVESTIGACIONES FARMACOLOGICAS
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Effects of early adverse life events on GABAergic neurons
Autor/es:
ADRIAN E SALATINO; MARIA MERCEDES ODEON; MARIA LUZ ORTA; GB ACOSTA
Lugar:
XLI Reunión Científica Anual de la Asociación Argentina de Farmacología Experimental (SAFE).
Reunión:
Congreso; XLI Reunión Científica Anual de la Asociación Argentina de Farmacología Experimental (SAFE).; 2009
Institución organizadora:
Asociacion Argentina de Farmacología Experimental
Resumen:
EFFECTS OF EARLY ADVERSE LIFE EVENTS ON GABAERGIC NEURONS Salatino AE, Odeón MM, Orta ML, Acosta GB. ININFA- (CONICET-UBA). Junín 956. 5th floor, C1113AAD, Buenos Aires. E-mail: adrian86@gmail.com Neonatal period may be an especially high risk period given the continued proliferation of neuronal cells and developmental of neuronal pathways. We investigate the consequences of repeated maternal separation and exposed to cold stress on brain development in order to determinate if the effects on GABAergic function were age-specific. Rats’ pups were separated from their mother plus cold exposure (4ºC) for 1h at postnatal (PD) 5, 7, 13 and 21 during 20 days (wash-out period: 30d). The rats were killed by decapitation and trunk blood samples were collected to measure corticosterone levels. Frontal cortex (FC) and hippocampus (HIC) were dissected in order to study GABA uptake. Also we used Western blotting to evaluate the alterations in the expression of HIC and FC GAT-1. Our results shows that the time course of repeated stress decreased GABA uptake in FC at PD5 and HIC at PD13. At PD5 we found a decreased GAT-1 level in HIC and increased in FC. Chronic stress altered the basal levels of corticosterone at the different ages studied. These results support the notion that the development of the FC is affected by stressors during early life. The findings are in agreement with the hypothesis of compensatory changes development in response to repeated stress, we would propose a FC as key in the development of adaptative mechanisms.