Synaptic expression of glutamate receptor after encoding of fear memory in the rat amygdala.
- Authors
- Yeh, Shiu-Hwa; Mao, Sheng-Chun; Lin, Hui-Ching; Gean, Po-Wu
- Year
- 2006
- Journal
- Molecular pharmacology
- PMID
- 16219906
- DOI
- 10.1124/mol.105.017194
Fear conditioning has been ascribed to presynaptic mechanisms, particularly presynaptic facilitation of transmission at thalamo- and cortico-amygdala synapses. Here, by labeling surface receptors with biotin or using membrane fractionation approaches, we report that fear conditioning resulted in an increase in surface expression of GluR1 subunit of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors in the amygdala, whereas total GluR1 mRNA and protein levels were unchanged. The control group that received conditioned stimulus (CS) and unconditioned stimulus in an unpaired fashion did not present any increase, indicating that GluR1 increase was specific to the learning component of the task. Conditioning-induced increase in surface expression of GluR1 depended on the activation of N-methyl-d-aspartate receptors and protein kinases and required the synthesis of new proteins. CS-alone trials applied 24 h before training attenuated fear-potentiated startle and prevented conditioning-induced increase in surface expression of GluR1. Increase in GluR1 was also observed in the amygdala slices after delivery of tetanic stimulation that elicited long-term potentiation of synaptic transmission. Proteasome inhibitor increased surface expression of GluR1 in a time- and dose-dependent manner. Furthermore, pretraining administration of proteasome inhibitor into the amygdala facilitated the fear-potentiated startle. These results suggest that long-term memory formation is correlated with the change in synaptic expression of GluR1, and trafficking of GluR1 to the synaptic sites contributes at least in part to the expression of fear memory.
No figures extracted from this document.
No chunks β full text not yet ingested.
No entities extracted from this document yet.
No uploaded files.
No citations found.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Fear Learning: An Evolving Picture for Plasticity at Synaptic Afferents to the Amygdala. | Palchaudhuri S et al. | β | 2024 | β |
| Amygdala Intercalated Cells: Gate Keepers and Conveyors of Internal State to the Circuits of Emotion. | Asede D et al. | β | 2022 | β |
| Fear learning-induced changes in AMPAR and NMDAR expression in the fear circuit. | Shultz B et al. | β | 2022 | β |
| Know thy SEFL: Fear sensitization and its relevance to stressor-related disorders. | Nishimura KJ et al. | β | 2022 | β |
| Sex differences in training-induced activity of the ubiquitin proteasome system in the dorsal hippocampus and medial prefrontal cortex of male and female mice. | Beamish SB et al. | β | 2022 | β |
| Fear Memory Retrieval Is Associated With a Reduction in AMPA Receptor Density at Thalamic to Amygdala Intercalated Cell Synapses. | Seewald A et al. | β | 2021 | β |
| Lack of Parkinsonian Pathology and Neurodegeneration in Mice After Long-Term Injections of a Proteasome Inhibitor in Olfactory Bulb and Amygdala. | Del Rey NL et al. | β | 2021 | β |
| Males and females differ in the regulation and engagement of, but not requirement for, protein degradation in the amygdala during fear memory formation. | Devulapalli R et al. | β | 2021 | β |
| Ubiquitin and Ubiquitin-Like Proteins in the Critical Equilibrium between Synapse Physiology and Intellectual Disability. | Folci A et al. | β | 2020 | β |
| Chronic over-expression of ubiquitin impairs learning, reduces synaptic plasticity, and enhances GRIA receptor turnover in mice. | Vaden JH et al. | β | 2019 | β |
| GluR2 endocytosis-dependent protein degradation in the amygdala mediates memory updating. | Ferrara NC et al. | β | 2019 | β |
| Danger Changes the Way the Mammalian Brain Stores Information About Innocuous Events: A Study of Sensory Preconditioning in Rats. | Holmes NM et al. | β | 2018 | β |
| The dynamic nature of fear engrams in the basolateral amygdala. | Davis P et al. | β | 2018 | β |
| The Role of Actin Cytoskeleton in Dendritic Spines in the Maintenance of Long-Term Memory. | Basu S et al. | β | 2018 | β |
| Histone deacetylase inhibition induces odor preference memory extension and maintains enhanced AMPA receptor expression in the rat pup model. | Bhattacharya S et al. | β | 2017 | β |
| Input from the medial geniculate nucleus modulates amygdala encoding of fear memory discrimination. | Ferrara NC et al. | β | 2017 | β |
| Dynamics of Hippocampal Protein Expression During Long-term Spatial Memory Formation. | Borovok N et al. | β | 2016 | β |
| Evidence of CNIH3 involvement in opioid dependence. | Nelson EC et al. | β | 2016 | β |
| Fear potentiated startle increases phospholipase D (PLD) expression/activity and PLD-linked metabotropic glutamate receptor mediated post-tetanic potentiation in rat amygdala. | Krishnan B et al. | β | 2016 | β |
| The Role of Actin Cytoskeleton in Memory Formation in Amygdala. | Lamprecht R | β | 2016 | β |
| The Role of Ephs and Ephrins in Memory Formation. | Dines M et al. | β | 2016 | β |
| Acquisition of conditioned fear is followed by region-specific changes in RNA editing of glutamate receptors. | Brande-Eilat N et al. | β | 2015 | β |
| Brain sites involved in fear memory reconsolidation and extinction of rodents. | Baldi E et al. | β | 2015 | β |
| Differences in long-term memory stability and AmCREB level between forward and backward conditioned honeybees (Apis mellifera). | Felsenberg J et al. | β | 2015 | β |
| Memory retrieval requires ongoing protein synthesis and NMDA receptor activity-mediated AMPA receptor trafficking. | Lopez J et al. | β | 2015 | β |
| The Membrane Proximal Region of AMPA Receptors in Lateral Amygdala is Essential for Fear Memory Formation. | Ganea DA et al. | β | 2015 | β |
| Hippocampal biomarkers of fear memory in an animal model of generalized anxiety disorder. | Dias GP et al. | β | 2014 | β |
| Impact of combined prenatal ethanol and prenatal stress exposures on markers of activity-dependent synaptic plasticity in rat dentate gyrus. | Staples MC et al. | β | 2014 | β |
| Protein degradation and protein synthesis in long-term memory formation. | Jarome TJ et al. | β | 2014 | β |
| The actin cytoskeleton in memory formation. | Lamprecht R | β | 2014 | β |
| CaMKII, but not protein kinase A, regulates Rpt6 phosphorylation and proteasome activity during the formation of long-term memories. | Jarome TJ et al. | β | 2013 | β |
| Depletion of serotonin in the basolateral amygdala elevates glutamate receptors and facilitates fear-potentiated startle. | Tran L et al. | β | 2013 | β |
| Inhibition of spontaneous recovery of fear by mGluR5 after prolonged extinction training. | Mao SC et al. | β | 2013 | β |
| Scaffolding proteins of the post-synaptic density contribute to synaptic plasticity by regulating receptor localization and distribution: relevance for neuropsychiatric diseases. | Iasevoli F et al. | β | 2013 | β |
| The beneficial effects of leptin on REM sleep deprivation-induced cognitive deficits in mice. | Chang HF et al. | β | 2013 | β |
| The ubiquitin-proteasome system as a critical regulator of synaptic plasticity and long-term memory formation. | Jarome TJ et al. | β | 2013 | β |
| The ubiquitin-specific protease 14 (USP14) is a critical regulator of long-term memory formation. | Jarome TJ et al. | β | 2013 | β |
| A role of protein degradation in memory consolidation after initial learning and extinction learning in the honeybee (Apis mellifera). | Felsenberg J et al. | β | 2012 | β |
| Postsynaptic BDNF signalling regulates long-term potentiation at thalamo-amygdala afferents. | Meis S et al. | β | 2012 | β |
| Re-exposure and environmental enrichment reveal NPY-Y1 as a possible target for post-traumatic stress disorder. | Hendriksen H et al. | β | 2012 | β |
| Stability of presynaptic vesicle pools and changes in synapse morphology in the amygdala following fear learning in adult rats. | Ostroff LE et al. | β | 2012 | β |
| The E3 ligase APC/C-Cdh1 is required for associative fear memory and long-term potentiation in the amygdala of adult mice. | Pick JE et al. | β | 2012 | β |
| Basolateral amygdala inactivation impairs learned (but not innate) fear response in rats. | Ribeiro AM et al. | β | 2011 | β |
| Dysregulated postsynaptic density and endocytic zone in the amygdala of human heroin and cocaine abusers. | Okvist A et al. | β | 2011 | β |
| Modulation of fear memory by retrieval and extinction: a clue for memory deconsolidation. | Hong I et al. | β | 2011 | β |
| Molecular mechanisms of fear learning and memory. | Johansen JP et al. | β | 2011 | β |
| Protein degradation and memory formation. | Fioravante D et al. | β | 2011 | β |
| Reversible plasticity of fear memory-encoding amygdala synaptic circuits even after fear memory consolidation. | Hong I et al. | β | 2011 | β |
| The roles of the actin cytoskeleton in fear memory formation. | Lamprecht R | β | 2011 | β |
| Alterations of excitatory transmission in the lateral amygdala during expression and extinction of fear memory. | Lin HC et al. | β | 2010 | β |
| AMPA receptor trafficking and learning. | Keifer J et al. | β | 2010 | β |
| Endogenous GluR1-containing AMPA receptors translocate to asymmetric synapses in the lateral amygdala during the early phase of fear memory formation: an electron microscopic immunocytochemical study. | Nedelescu H et al. | β | 2010 | β |
| Evidence for the persistence of contextual fear memories following immediate extinction. | Archbold GE et al. | β | 2010 | β |
| Interaction between N-ethylmaleimide-sensitive factor and GluR2 is essential for fear memory formation in lateral amygdala. | Joels G et al. | β | 2010 | β |
| Plastic synaptic networks of the amygdala for the acquisition, expression, and extinction of conditioned fear. | Pape HC et al. | β | 2010 | β |
| Synaptic plasticity and NO-cGMP-PKG signaling regulate pre- and postsynaptic alterations at rat lateral amygdala synapses following fear conditioning. | Ota KT et al. | β | 2010 | β |
| Ubiquitination in postsynaptic function and plasticity. | Mabb AM et al. | β | 2010 | β |
| Evaluation of the pro-cognitive effects of the AMPA receptor positive modulator, 5-(1-piperidinylcarbonyl)-2,1,3-benzoxadiazole (CX691), in the rat. | Woolley ML et al. | β | 2009 | β |
| Reduced expression of the NMDA receptor-interacting protein SynGAP causes behavioral abnormalities that model symptoms of Schizophrenia. | Guo X et al. | β | 2009 | β |
| Synaptic AMPA receptor plasticity and behavior. | Kessels HW et al. | β | 2009 | β |
| Augmentation of fear extinction by D-cycloserine is blocked by proteasome inhibitors. | Mao SC et al. | β | 2008 | β |
| Decreased AMPA GluR2, but not GluR3, mRNA expression in rat amygdala and dorsal hippocampus following morphine-induced behavioural sensitization. | Sepehrizadeh Z et al. | β | 2008 | β |
| Disruption of AMPA receptor endocytosis impairs the extinction, but not acquisition of learned fear. | Dalton GL et al. | β | 2008 | β |
| Amygdala depotentiation and fear extinction. | Kim J et al. | β | 2007 | β |
| A pathway-specific function for different AMPA receptor subunits in amygdala long-term potentiation and fear conditioning. | Humeau Y et al. | β | 2007 | β |
| Chronic ethanol and withdrawal differentially modulate pre- and postsynaptic function at glutamatergic synapses in rat basolateral amygdala. | LΓ€ck AK et al. | β | 2007 | β |
| Impaired associative fear learning in mice with complete loss or haploinsufficiency of AMPA GluR1 receptors. | Feyder M et al. | β | 2007 | β |
| Long-term memory consolidation depends on proteasome activity in the crab Chasmagnathus. | Merlo E et al. | β | 2007 | β |
| Long-term potentiation in the amygdala: a cellular mechanism of fear learning and memory. | Sigurdsson T et al. | β | 2007 | β |
| NAC1 regulates the recruitment of the proteasome complex into dendritic spines. | Shen H et al. | β | 2007 | β |
| Training-induced changes in the expression of GABAA-associated genes in the amygdala after the acquisition and extinction of Pavlovian fear. | Heldt SA et al. | β | 2007 | β |
| Extinction training in conjunction with a partial agonist of the glycine site on the NMDA receptor erases memory trace. | Mao SC et al. | β | 2006 | β |