Back to Search
Start Over
Targeting fear memories: Examining pharmacological disruption in a generalized fear framework.
- Source :
-
Neurobiology of learning and memory [Neurobiol Learn Mem] 2024 Sep; Vol. 213, pp. 107960. Date of Electronic Publication: 2024 Jul 14. - Publication Year :
- 2024
-
Abstract
- Labilization-reconsolidation, which relies on retrieval, has been considered an opportunity to attenuate the negative aspects of traumatic memories. A therapeutic strategy based on reconsolidation blockade is deemed more effective than current therapies relying on memory extinction. Nevertheless, extremely stressful memories frequently prove resistant to this process. Here, after inducing robust fear memory in mice through strong fear conditioning, we examined the possibility of rendering it susceptible to pharmacological modulation based on the degree of generalized fear (GF). To achieve this, we established an ordered gradient of GF, determined by the perceptual similarity between the associated context (CA) and non-associated contexts (CB, CC, CD, and CE) to the aversive event. We observed that as the exposure context became less similar to CA, the defensive pattern shifted from passive to active behaviors in both male and female mice. Subsequently, in conditioned animals, we administered propranolol after exposure to the different contexts (CA, CB, CC, CD or CE). In males, propranolol treatment resulted in reduced freezing time and enhanced risk assessment behaviors when administered following exposure to CA or CB, but not after CC, CD, or CE, compared to the control group. In females, a similar change in behavioral pattern was observed with propranolol administered after exposure to CC, but not after the other contexts. These results highlight the possibility of indirectly manipulating a robust contextual fear memory by controlling the level of generalization during recall. Additionally, it was demonstrated that the effect of propranolol on reconsolidation would not lead to a reduction in fear memory per se, but rather to its reorganization resulting in greater behavioral flexibility (from passive to active behaviors). Finally, from a clinical viewpoint, this would be of considerable relevance since following this strategy could make the treatment of psychiatric disorders associated with traumatic memory formation more effective and less stressful.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Stress Disorders, Post-Traumatic psychology
Stress Disorders, Post-Traumatic rehabilitation
Stress Disorders, Post-Traumatic therapy
Male
Female
Mice
Conditioning, Classical drug effects
Avoidance Learning drug effects
Memory Consolidation drug effects
Generalization, Response drug effects
Behavior, Animal drug effects
Arousal drug effects
Freezing Reaction, Cataleptic drug effects
Electroshock
Fear drug effects
Fear physiology
Fear psychology
Memory drug effects
Memory physiology
Propranolol administration & dosage
Propranolol pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9564
- Volume :
- 213
- Database :
- MEDLINE
- Journal :
- Neurobiology of learning and memory
- Publication Type :
- Academic Journal
- Accession number :
- 39004160
- Full Text :
- https://doi.org/10.1016/j.nlm.2024.107960