Volume 10 Supplement 1
Fear learning triggers structural changes at GABAergic synapses in the basal amygdala
© Ferraguti et al; licensee BioMed Central Ltd. 2010
Published: 16 November 2010
In Pavlovian fear conditioning, in which initially a conditioned stimulus (CS) is repeatedly paired with an aversive stimulus (US), animals learn to associate CS with US, hence attaching emotional significance to sensory stimuli. Conditioned fear can be suppressed when the CS is repeatedly presented alone, a phenomenon known as fear extinction. Previous studies suggest that the mechanisms underlying fear conditioning involve inhibitory neurotransmission through GABAA receptors. GABAA receptors are generally composed of two α, two β and one γ subunits. Sixteen GABAA receptor subunits have been identified in mammals, which indicates that these receptors may have multiple biophysical and pharmacological properties. Recent work showed that fear conditioning induces a dramatic downregulation of benzodiazepine binding sites and transcripts for gephyrin and some GABAA receptor subunits in the basal nucleus of the amygdala (BA), which were restored to control levels after fear extinction.
In this work, we analysed by means of the freeze-fracture replica immunolabelling technique (SDS-FRL) the synaptic and extrasynaptic content of the GABAA-γ2 subunit in the BA of C57BL/6 mice that underwent fear conditioning as well as extinction. Using this technique, we could also measure the full synaptic area of GABAergic synapses. Immunogold particles for GABAA subunits tend to concentrate in clusters of intramembrane particles (IMP) on the protoplasmic face of the plasma membrane, indicating that labelled IMP clusters represent GABAergic synapses.
The average size of GABAergic synapses in control mice was 0.030 ± 0.019 μm2 (n = 223). The mean synaptic size (0.040 ± 0.025 μm2, n = 198) in fear conditioned animals was significantly (p < 0.0001, one-way ANOVA) increased, whereas in mice that underwent extinction it returned to values similar to those of controls (0.032 ± 0.021 μm2, n = 154). The distribution frequency of the area of GABAergic synapses was also found to be significantly different between fear conditioned and control mice (p < 0.01). The labelling density for the GABAA-γ2 subunit was significantly lower in both synaptic (p < 0.05, Kruskal-Wallis) and extrasynaptic (p < 0.05, Kruskal-Wallis) areas in fear conditioned animals. However, the decrease in synaptic density appears to be a consequence of the increased synaptic area.
These results suggest that in normal animals fear conditioning produces an enlargement of GABAergic synapses maintaining the number of GABAA receptors substantially unaltered.
This article is published under license to BioMed Central Ltd.