AI Article Synopsis

  • - Auditory fear conditioning in rodents pairs a neutral sound with an unpleasant experience to create a fear memory, relying on long-term potentiation (LTP) in the lateral amygdala and the creation of new proteins.
  • - While many past studies have looked at specific proteins' roles in LTP and fear learning, recent genome-wide studies have limitations in measuring protein level changes.
  • - This study used quantitative proteomics to analyze the protein expression in the lateral amygdala during auditory fear conditioning and identified numerous proteins related to LTP and learning, including many that haven't been previously linked to these processes.

Article Abstract

Auditory fear conditioning is a well-characterized rodent learning model where a neutral auditory cue is paired with an aversive outcome to induce associative fear memory. The storage of long-term auditory fear memory requires long-term potentiation (LTP) in the lateral amygdala and de novo protein synthesis. Although many studies focused on individual proteins have shown their contribution to LTP and fear conditioning, non-biased genome-wide studies have only recently been possible with microarrays, which nevertheless fall short of measuring changes at the level of proteins. Here we employed quantitative proteomics to examine the expression of hundreds of proteins in the lateral amygdala in response to auditory fear conditioning. We found that various proteins previously implicated in LTP, learning and axon/dendrite growth were regulated by fear conditioning. A substantial number of proteins that were regulated by fear conditioning have not yet been studied specifically in learning or synaptic plasticity.

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Source
http://dx.doi.org/10.1016/j.bbrc.2013.03.060DOI Listing

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