Izquierdo I, Bianchin M, Silva M B, Zanatta M S, Walz R, Ruschel A C, Da Silva R C, Paczko N, Medina J H
Departamento de Bioquimica, Instituto de Biociencias, U.F.R.G.S., Porto Alegre, RS, Brazil.
Behav Neural Biol. 1993 Jan;59(1):1-4. doi: 10.1016/0163-1047(93)91061-q.
The bilateral infusion of CNQX (0.5 or 1.25 micrograms) into the amygdala or dorsal hippocampus 10 min prior to a retention test partially blocked the expression of stepdown inhibitory avoidance in rats 24 h after training. When infused into both the amygdala and the hippocampus at a dose of 0.5 microgram. CNQX caused a complete blockade of the expression of that task. Retention test performance recovered 2 h after the infusions. In rats trained for habituation to a novel environment and tested 24 h later, pretest intrahippocampal CNQX (0.5 microgram) blocked the expression of retention at a dose of 0.5 microgram, and intra-amygdala CNQX (0.5 or 1.25 micrograms) had no effect. The data suggest that, up to at least 1 day after training, memory of the avoidance task depends on glutamate acting on non-NMDA receptors in both the hippocampus and the amygdala, whereas memory of the habituation task depends on non-NMDA receptor activity in the hippocampus but not the amygdala.