Reactivation-dependent transfer of fear memory between contexts requires M1 muscarinic receptor stimulation in dorsal hippocampus of male rats.

IF 1.8 4区 医学 Q4 NEUROSCIENCES Learning & memory Pub Date : 2024-10-09 Print Date: 2024-09-01 DOI:10.1101/lm.054039.124
Karim H Abouelnaga, Andrew E Huff, Kristen H Jardine, Olivia S O'Neill, Boyer D Winters
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Abstract

Memory updating is essential for integrating new information into existing representations. However, this process could become maladaptive in conditions like post-traumatic stress disorder (PTSD), when fear memories generalize to neutral contexts. Previously, we have shown that contextual fear memory malleability in rats requires activation of M1 muscarinic acetylcholine receptors in the dorsal hippocampus. Here, we investigated the involvement of this mechanism in the transfer of contextual fear memories to other contexts using a novel fear memory updating paradigm. Following brief reexposure to a previously fear conditioned context, male rats (n = 8-10/group) were placed into a neutral context to evaluate the transfer of fear memory. We also infused the selective M1 receptor antagonist pirenzepine into the dorsal hippocampus before memory reactivation to try to block this effect. Results support the hypothesis that fear memory can be updated with novel contextual information, but only if rats are reexposed to the originally trained context relatively recently before the neutral context; evidence for transfer was not seen if the fear memory reactivation was omitted or if it occurred 6 h before neutral context exposure. The transferred fear persisted for 4 weeks, and the effect was blocked by M1 antagonism. These findings strongly suggest that fear transfer requires reactivation and destabilization of the original fear memory. The novel preclinical model introduced here, and its implication of muscarinic receptors in this process, could therefore inform therapeutic strategies for PTSD and similar conditions.

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雄性大鼠海马背侧的恐惧记忆在不同情境间的转移需要M1毒蕈碱受体的刺激。
记忆更新对于将新信息整合到现有表征中至关重要。然而,在创伤后应激障碍(PTSD)等情况下,当恐惧记忆泛化到中性情境时,这一过程可能会变得不适应。此前,我们已经证明,大鼠的情境恐惧记忆延展性需要激活海马背侧的M1毒蕈碱乙酰胆碱受体。在这里,我们使用一种新的恐惧记忆更新范式研究了这种机制在将情境恐惧记忆转移到其他情境时的参与作用。雄性大鼠(n = 8-10只/组)在短暂重新暴露于先前的恐惧条件情境后,会被置于中性情境中,以评估恐惧记忆的转移。我们还在记忆重新激活前将选择性 M1 受体拮抗剂哌仑西平注入背侧海马,试图阻断这种效应。结果支持这样的假设,即恐惧记忆可以通过新的情境信息得到更新,但前提是大鼠在中性情境暴露之前相对较近的时间内重新暴露于原先训练过的情境;如果省略恐惧记忆的重新激活或在中性情境暴露之前 6 小时重新激活,则看不到转移的证据。转移的恐惧持续了 4 周,这种效应被 M1 拮抗剂阻断。这些发现有力地表明,恐惧转移需要原始恐惧记忆的重新激活和不稳定。因此,本文介绍的新型临床前模型及其对这一过程中毒蕈碱受体的影响,可以为创伤后应激障碍和类似疾病的治疗策略提供参考。
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来源期刊
Learning & memory
Learning & memory 医学-神经科学
CiteScore
3.60
自引率
5.00%
发文量
45
审稿时长
6-12 weeks
期刊介绍: The neurobiology of learning and memory is entering a new interdisciplinary era. Advances in neuropsychology have identified regions of brain tissue that are critical for certain types of function. Electrophysiological techniques have revealed behavioral correlates of neuronal activity. Studies of synaptic plasticity suggest that some mechanisms of memory formation may resemble those of neural development. And molecular approaches have identified genes with patterns of expression that influence behavior. It is clear that future progress depends on interdisciplinary investigations. The current literature of learning and memory is large but fragmented. Until now, there has been no single journal devoted to this area of study and no dominant journal that demands attention by serious workers in the area, regardless of specialty. Learning & Memory provides a forum for these investigations in the form of research papers and review articles.
期刊最新文献
The influence of categorical stimuli on relational memory binding. Dysregulating mTORC1-4E-BP2 signaling in GABAergic interneurons impairs hippocampus-dependent learning and memory. Reactivation-dependent transfer of fear memory between contexts requires M1 muscarinic receptor stimulation in dorsal hippocampus of male rats. Domain-selective and sex-dependent regulation of learning and memory in mice by GIRK channel activity in CA1 pyramidal neurons of the dorsal hippocampus. Sex and the facilitation of cued fear by prior contextual fear conditioning in rats.
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