Gulmez Karaca Kubra, Bahtiyar Sevgi, van Dongen Linde, Wolf Oliver T, Hermans Erno J, Henckens Marloes J A G, Roozendaal Benno
Department of Medical Neuroscience, Radboud university medical center, 6500 HB, Nijmegen, The Netherlands.
Donders Institute for Brain, Cognition and Behaviour, Radboud University, 6525 EN, Nijmegen, The Netherlands.
Neuropsychopharmacology. 2025 May 8. doi: 10.1038/s41386-025-02122-2.
Recent findings indicate that noradrenergic arousal maintains long-term episodic-like specificity of memory. However, the neural mechanism of how norepinephrine can alter the temporal dynamics of systems consolidation to maintain hippocampus dependency of remote memory is currently unknown. Memories are stored within ensembles of neurons that become activated during learning and display strengthened mutual plasticity and connectivity. This strengthened connectivity is believed to guide the coordinated reactivation of these neurons upon subsequent memory recall. Here, we used male transgenic FosTRAP2xtdTomato mice to investigate whether the noradrenergic stimulant yohimbine administered systemically immediately after an episodic-like object-in-context training experience maintained long-term memory specificity which was joined by an enhanced reactivation of training-activated cells within the hippocampus during remote retention testing. We found that saline-treated control mice time-dependently lost their episodic-like specificity of memory, which was associated with a shift in neuronal reactivation from the dorsal hippocampus to the prelimbic cortex at a 14-day retention test. Importantly, yohimbine-treated mice maintained episodic-like specificity of remote memory and retained high neuronal reactivation within the dorsal hippocampus, without a time-dependent increase in prelimbic cortex reactivation. These findings suggest that noradrenergic arousal shortly after training maintains episodic-like specificity of remote memory by strengthening the connectivity between training-activated hippocampal cells during consolidation, and provide a cellular model of how emotional memories remain vivid and detailed.
最近的研究结果表明,去甲肾上腺素能唤醒维持记忆的长期情景样特异性。然而,去甲肾上腺素如何改变系统巩固的时间动态以维持远程记忆对海马体的依赖性,其神经机制目前尚不清楚。记忆存储在学习过程中被激活的神经元集合中,并表现出增强的相互可塑性和连接性。这种增强的连接性被认为在随后的记忆回忆时引导这些神经元的协同再激活。在这里,我们使用雄性转基因FosTRAP2xtdTomato小鼠来研究,在进行情景样的情境中物体训练后立即全身给予去甲肾上腺素能兴奋剂育亨宾,是否能维持长期记忆特异性,以及在远程保留测试期间海马体内训练激活细胞的再激活增强是否与之相关。我们发现,生理盐水处理的对照小鼠随时间推移失去了它们的情景样记忆特异性,这与在14天的保留测试中神经元再激活从背侧海马体转移到前边缘皮层有关。重要的是,育亨宾处理的小鼠维持了远程记忆的情景样特异性,并在背侧海马体内保持了较高的神经元再激活,而前边缘皮层的再激活没有随时间增加。这些发现表明,训练后不久的去甲肾上腺素能唤醒通过在巩固过程中加强训练激活的海马体细胞之间的连接性,维持了远程记忆的情景样特异性,并提供了一个关于情感记忆如何保持生动和详细的细胞模型。