P2X7 receptors modulate acquisition of cue fear extinction and contextual background memory generalization in male mice

The purinergic P2X7 receptors (P2X7R) are activated by adenosine triphosphate (ATP) in several brain regions, particularly those involved with emotional control and the regulation of fear-related memories. Here, we investigate the role of P2X7R in fear learning memory, specifically in the acquisition and consolidation phases of the cued fear conditioning paradigm. C57Bl/6 wildtype (WT) male mice that received a single i.p. injection of the selective P2X7R antagonist A438079 prior the conditioning session showed generalization of cued fear memory and impaired fear extinction recall in the test session, while those treated prior the extinction session exhibited a similar behavior profile accompanied by resistance in the extinction learning. However, no effects were observed when this drug was administered immediately after the conditioning, extinction, or before the test session. Our results with P2X7R knockout (P2X7 KO) mice showed a behavioral profile that mirrored the collective effects observed across all pharmacological treatment conditions. This suggests that the P2X7R KO model effectively replicates the behavioral changes induced by the pharmacological interventions, demonstrating that we have successfully isolated the role of P2X7R in the fear and extinction phases of memory. These findings highlight the role of P2X7R in the acquisition and recall of extinction memory and supports P2X7R as a promising candidate for controlling abnormal fear processing, with potential applications for stress exposure-related disorders such as post-traumatic stress disorder (PTSD).

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Publication Details

Journal
Neuropharmacology
Published
2024-10-02
DOI
https://doi.org/10.1016/j.neuropharm.2024.110177
Citations
6
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
1.61

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article

P2X7 receptors modulate acquisition of cue fear extinction and contextual background memory generalization in male mice

Jéssica Rosa, Ana Luisa B. Terzian, Leonardo B.M. Resstel, Cassiano R.A.F. Diniz et al.
6 citations
Neuropharmacology
Neuroscience and Neuropharmacology Research
1.61
article

P2X7 receptors modulate acquisition of cue fear extinction and contextual background memory generalization in male mice

Jéssica Rosa, Ana Luisa B. Terzian, Leonardo B.M. Resstel, Cassiano R.A.F. Diniz, Luana B. Domingos, Antonio Furtado da Silva Júnior
article en
6 citations

Abstract

The purinergic P2X7 receptors (P2X7R) are activated by adenosine triphosphate (ATP) in several brain regions, particularly those involved with emotional control and the regulation of fear-related memories. Here, we investigate the role of P2X7R in fear learning memory, specifically in the acquisition and consolidation phases of the cued fear conditioning paradigm. C57Bl/6 wildtype (WT) male mice that received a single i.p. injection of the selective P2X7R antagonist A438079 prior the conditioning session showed generalization of cued fear memory and impaired fear extinction recall in the test session, while those treated prior the extinction session exhibited a similar behavior profile accompanied by resistance in the extinction learning. However, no effects were observed when this drug was administered immediately after the conditioning, extinction, or before the test session. Our results with P2X7R knockout (P2X7 KO) mice showed a behavioral profile that mirrored the collective effects observed across all pharmacological treatment conditions. This suggests that the P2X7R KO model effectively replicates the behavioral changes induced by the pharmacological interventions, demonstrating that we have successfully isolated the role of P2X7R in the fear and extinction phases of memory. These findings highlight the role of P2X7R in the acquisition and recall of extinction memory and supports P2X7R as a promising candidate for controlling abnormal fear processing, with potential applications for stress exposure-related disorders such as post-traumatic stress disorder (PTSD).

NeuropharmacologyVol. 261
Universidade de Ribeirão Preto (BR), University of Eastern Finland (FI), Universidade de São Paulo (BR), Aarhus University (DK)
Fundação de Amparo à Pesquisa do Estado de São Paulo
Openalex Percentile: Top 17%
Neuroscience and Neuropharmacology Research
1.61
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