| Literature DB >> 31543297 |
Yu Kasugai1, Elisabeth Vogel2, Heide Hörtnagl1, Sabine Schönherr1, Enrica Paradiso1, Markus Hauschild3, Georg Göbel4, Ivan Milenkovic5, Yvan Peterschmitt6, Ramon Tasan1, Günther Sperk1, Ryuichi Shigemoto7, Werner Sieghart5, Nicolas Singewald3, Andreas Lüthi8, Francesco Ferraguti9.
Abstract
Associative learning is thought to involve different forms of activity-dependent synaptic plasticity. Although previous studies have mostly focused on learning-related changes occurring at excitatory glutamatergic synapses, we found that associative learning, such as fear conditioning, also entails long-lasting functional and structural plasticity of GABAergic synapses onto pyramidal neurons of the murine basal amygdala. Fear conditioning-mediated structural remodeling of GABAergic synapses was associated with a change in mIPSC kinetics and an increase in the fraction of synaptic benzodiazepine-sensitive (BZD) GABAA receptors containing the α2 subunit without altering the intrasynaptic distribution and overall amount of BZD-GABAA receptors. These structural and functional synaptic changes were partly reversed by extinction training. These findings provide evidence that associative learning, such as Pavlovian fear conditioning and extinction, sculpts inhibitory synapses to regulate inhibition of active neuronal networks, a process that may tune amygdala circuit responses to threats.Entities:
Keywords: GABA; GABA(A) receptors; extinction; freeze-fracture; gating kinetics; inhibition; learning; plasticity; synapse
Mesh:
Year: 2019 PMID: 31543297 DOI: 10.1016/j.neuron.2019.08.013
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173