Amygdalo-cortical dialogue underlies memory enhancement by emotional association.

IF 15 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2025-03-19 Epub Date: 2025-01-29 DOI:10.1016/j.neuron.2025.01.001
Yoshihito Saito, Yuma Osako, Maya Odagawa, Yasuhiro Oisi, Chie Matsubara, Shigeki Kato, Kazuto Kobayashi, Mitsuhiro Morita, Joshua P Johansen, Masanori Murayama
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Abstract

Emotional arousal plays a critical role in determining what is remembered from experiences. It is hypothesized that activation of the amygdala by emotional stimuli enhances memory consolidation in its downstream brain regions. However, the physiological basis of the inter-regional interaction and its functions remain unclear. Here, by adding emotional information to a perceptual recognition task that relied on a frontal-sensory cortical circuit in mice, we demonstrated that the amygdala not only associates emotional information with perceptual information but also enhances perceptual memory retention via amygdalo-frontal cortical projections. Furthermore, emotional association increased reactivation of coordinated activity across the amygdalo-cortical circuit during non-rapid eye movement (NREM) sleep but not during rapid eye movement (REM) sleep. Notably, this increased reactivation was associated with amygdala high-frequency oscillations. Silencing of amygdalo-cortical inputs during NREM sleep selectively disrupted perceptual memory enhancement. Our findings indicate that inter-regional reactivation triggered by the amygdala during NREM sleep underlies emotion-induced perceptual memory enhancement.

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杏仁核-皮层对话是通过情感联系增强记忆的基础。
情绪唤起在决定从经历中记住什么方面起着关键作用。据推测,情绪刺激激活杏仁核可以增强其下游大脑区域的记忆巩固。然而,区域间相互作用的生理基础及其功能尚不清楚。本研究通过将情感信息添加到依赖于小鼠额叶-感觉皮层回路的感知识别任务中,我们证明了杏仁核不仅将情感信息与感知信息联系起来,而且通过杏仁核-额叶皮层投射增强了感知记忆的保留。此外,在非快速眼动(NREM)睡眠期间,情绪关联增加了杏仁核-皮层回路协调活动的再激活,而在快速眼动(REM)睡眠期间则没有。值得注意的是,这种增加的再激活与杏仁核高频振荡有关。在非快速眼动睡眠期间,杏仁核皮层输入的沉默选择性地破坏了知觉记忆的增强。我们的研究结果表明,在非快速眼动睡眠期间,杏仁核触发的区域间再激活是情绪诱导的感知记忆增强的基础。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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