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血清素在非快速眼动睡眠期间调节齿状回中的超慢振荡。

Serotonin modulates infraslow oscillation in the dentate gyrus during non-REM sleep.

作者信息

Turi Gergely F, Teng Sasa, Chen Xinyue, Lim Emily C Y, Dias Carla, Hu Ruining, Wang Ruizhi, Zhen Fenghua, Peng Yueqing

机构信息

New York State Psychiatric Institute, Division of Systems Neuroscience New York, New York, United States.

Department of Psychiatry, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States.

出版信息

Elife. 2025 Apr 3;13:RP100196. doi: 10.7554/eLife.100196.

DOI:10.7554/eLife.100196
PMID:40178074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11968106/
Abstract

Synchronous neuronal activity is organized into neuronal oscillations with various frequency and time domains across different brain areas and brain states. For example, hippocampal theta, gamma, and sharp wave oscillations are critical for memory formation and communication between hippocampal subareas and the cortex. In this study, we investigated the neuronal activity of the dentate gyrus (DG) with optical imaging tools during sleep-wake cycles in mice. We found that the activity of major glutamatergic cell populations in the DG is organized into infraslow oscillations (0.01-0.03 Hz) during NREM sleep. Although the DG is considered a sparsely active network during wakefulness, we found that 50% of granule cells and about 25% of mossy cells exhibit increased activity during NREM sleep, compared to that during wakefulness. Further experiments revealed that the infraslow oscillation in the DG was correlated with rhythmic serotonin release during sleep, which oscillates at the same frequency but in an opposite phase. Genetic manipulation of 5-HT receptors revealed that this neuromodulatory regulation is mediated by receptors and the knockdown of these receptors leads to memory impairment. Together, our results provide novel mechanistic insights into how the 5-HT system can influence hippocampal activity patterns during sleep.

摘要

同步神经元活动被组织成具有不同频率和时域的神经元振荡,分布于不同脑区和脑状态。例如,海马体的θ波、γ波和尖波振荡对于记忆形成以及海马体亚区与皮层之间的通讯至关重要。在本研究中,我们使用光学成像工具在小鼠的睡眠-觉醒周期中研究了齿状回(DG)的神经元活动。我们发现,在非快速眼动睡眠期间,DG中主要谷氨酸能细胞群的活动被组织成超慢振荡(0.01-0.03赫兹)。尽管DG在清醒时被认为是一个活动稀疏的网络,但我们发现,与清醒时相比,50%的颗粒细胞和约25%的苔藓细胞在非快速眼动睡眠期间活动增加。进一步的实验表明,DG中的超慢振荡与睡眠期间有节奏的血清素释放相关,血清素以相同频率但相反相位振荡。对5-羟色胺受体的基因操作表明,这种神经调节是由受体介导的,敲低这些受体会导致记忆障碍。总之,我们的结果为5-羟色胺系统如何在睡眠期间影响海马体活动模式提供了新的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/a36add1e1f5d/elife-100196-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/a89721b9f00e/elife-100196-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/ea4c95a30be1/elife-100196-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/d121b3ab107e/elife-100196-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/407898a331ab/elife-100196-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/531845195619/elife-100196-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/1ef703b3e54e/elife-100196-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/502810914519/elife-100196-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/4d8b2d870a1c/elife-100196-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/4d6b6a7634b3/elife-100196-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/3c2e16dc38b4/elife-100196-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/0c06bc9d0db8/elife-100196-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/a36add1e1f5d/elife-100196-fig6-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/a89721b9f00e/elife-100196-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/ea4c95a30be1/elife-100196-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/d121b3ab107e/elife-100196-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/407898a331ab/elife-100196-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/531845195619/elife-100196-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/1ef703b3e54e/elife-100196-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/502810914519/elife-100196-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/4d8b2d870a1c/elife-100196-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/4d6b6a7634b3/elife-100196-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/3c2e16dc38b4/elife-100196-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/0c06bc9d0db8/elife-100196-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34e0/11968106/a36add1e1f5d/elife-100196-fig6-figsupp2.jpg

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