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

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Luana Barreto Domingos , Antonio Furtado da Silva Júnior , Cassiano Ricardo Alves Faria Diniz , Jessica Rosa , Ana Luisa B. Terzian , Leonardo Barbosa Moraes Resstel
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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).
P2X7受体调节雄性小鼠对线索恐惧消退和背景记忆泛化的获得。
嘌呤能 P2X7 受体(P2X7R)在多个脑区被三磷酸腺苷(ATP)激活,尤其是那些参与情绪控制和恐惧相关记忆调节的脑区。在这里,我们研究了 P2X7R 在恐惧学习记忆中的作用,特别是在诱导恐惧条件反射范式的获得和巩固阶段。C57Bl/6野生型(WT)雄性小鼠在条件反射前接受一次选择性P2X7R拮抗剂A438079的静脉注射后,在测试环节中表现出诱导恐惧记忆的泛化和恐惧消退回忆的受损,而在消退环节前接受治疗的小鼠则表现出类似的行为特征,并在消退学习中表现出抵抗。然而,如果在条件反射、消退后或测试前立即给药,则没有观察到任何影响。我们对 P2X7R 基因敲除(P2X7 KO)小鼠的研究结果显示,其行为特征与在所有药物治疗条件下观察到的集体效应一致。这表明 P2X7R KO 模型有效地复制了药理学干预所诱导的行为变化,证明我们已经成功地分离出 P2X7R 在记忆的恐惧和消退阶段的作用。这些发现强调了 P2X7R 在消减记忆的获得和回忆中的作用,并支持 P2X7R 成为控制异常恐惧处理的候选药物,有望应用于创伤后应激障碍(PTSD)等应激暴露相关疾病。
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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