TY - JOUR
T1 - P2X7 receptors modulate acquisition of cue fear extinction and contextual background memory generalization in male mice
AU - Domingos, Luana Barreto
AU - Silva Júnior, Antonio Furtado da
AU - Diniz, Cassiano Ricardo Alves Faria
AU - Rosa, Jessica
AU - Terzian, Ana Luisa B.
AU - Moraes Resstel, Leonardo Barbosa
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/12/15
Y1 - 2024/12/15
N2 - 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).
AB - 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).
KW - Acquisition
KW - Cued fear conditioning
KW - Extinction
KW - Generalization
KW - Memory
KW - P2X7 receptor
UR - http://www.scopus.com/inward/record.url?scp=85205488107&partnerID=8YFLogxK
U2 - 10.1016/j.neuropharm.2024.110177
DO - 10.1016/j.neuropharm.2024.110177
M3 - Journal article
C2 - 39366651
AN - SCOPUS:85205488107
SN - 0028-3908
VL - 261
JO - Neuropharmacology
JF - Neuropharmacology
M1 - 110177
ER -