Literature DB >> 29656024

Protein synthesis in the basolateral amygdala complex is required for consolidation of a first-order fear memory, but not for consolidation of a higher-order fear memory.

Dana M Leidl1, Belinda P P Lay1, Cassandra Chakouch1, R Frederick Westbrook1, Nathan M Holmes2.   

Abstract

The present series of experiments pursued our recent findings that consolidation of a second-order fear memory requires neuronal activity, but not de novo protein synthesis, in the basolateral amygdala complex (BLA). It used a modified second-order conditioning protocol in which rats were exposed to S1-shock pairings in stage 1 and pairings of the serial S2-S1 compound and shock in stage 2. Experiment 1 showed that responding (freezing) to S2 in this protocol is conditional on its compounding with S1 in stage 2 (Experiment 1), and therefore, the result of associative formation. The remaining experiments then showed that the protein synthesis requirement for consolidation of new learning about S2 varied with the training afforded S1. When S1 was trained in stage 1 and present in stage 2, consolidation of the new S2 fear memory was unaffected by pre- or post-stage 2 infusions of the protein synthesis inhibitor, cycloheximide, into the BLA (Experiments 2 and 5). This result was observed independently of the number of S1-shock pairings in stage 1 (even a single pairing produced the result), and alongside demonstrations that cycloheximide infusions disrupt consolidation of a first-order fear memory (Experiments 2 and 5). However, when S1 was not conditioned in stage 1 (Experiment 3) or was omitted from conditioning in stage 2 (Experiment 4), consolidation of the new S2 fear memory was disrupted by post-stage 2 cycloheximide infusions into the BLA. These results were taken to imply that the consolidation of a higher-order fear memory exploits molecular events associated with consolidation of a reactivated first-order fear memory; hence it occurs independently of de novo protein synthesis in the BLA. Alternatively, the nature of the association formed in higher-order conditioning may be such as to not require de novo protein synthesis for its consolidation.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Basolateral amygdala; Consolidation; Fear conditioning; Higher-order conditioning; Protein synthesis

Mesh:

Substances:

Year:  2018        PMID: 29656024     DOI: 10.1016/j.nlm.2018.04.001

Source DB:  PubMed          Journal:  Neurobiol Learn Mem        ISSN: 1074-7427            Impact factor:   2.877


  4 in total

1.  The Conditions under Which Consolidation of Serial-Order Conditioned Fear Requires De Novo Protein Synthesis in the Basolateral Amygdala Complex.

Authors:  Matthew J Williams-Spooner; R Frederick Westbrook; Nathan M Holmes
Journal:  J Neurosci       Date:  2019-07-24       Impact factor: 6.167

2.  Prediction Error Determines Whether NMDA Receptors in the Basolateral Amygdala Complex Are Involved in Pavlovian Fear Conditioning.

Authors:  Matthew J Williams-Spooner; Andrew J Delaney; R Frederick Westbrook; Nathan M Holmes
Journal:  J Neurosci       Date:  2022-04-11       Impact factor: 6.709

Review 3.  Understanding Associative Learning Through Higher-Order Conditioning.

Authors:  Dilara Gostolupce; Belinda P P Lay; Etienne J P Maes; Mihaela D Iordanova
Journal:  Front Behav Neurosci       Date:  2022-04-18       Impact factor: 3.617

4.  'Online' integration of sensory and fear memories in the rat medial temporal lobe.

Authors:  Francesca S Wong; R Fred Westbrook; Nathan M Holmes
Journal:  Elife       Date:  2019-06-10       Impact factor: 8.140

  4 in total

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