Evidence map›Paper›PMID 36272414›Full record

ArticleNeuron2022

REM sleep-active hypothalamic neurons may contribute to hippocampal social-memory consolidation.

Han Qin, Ling Fu, Tingliang Jian, Wenjun Jin, Mengru Liang, Jin Li, Qianwei Chen, Xinyu Yang, Haoran Du, Xiang Liao and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in Neuron, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

40 citing papers in PubMed.

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  5. Caffeine reverses sleep deprivation-induced synaptic and social memory deficits via adenosine receptor modulation in the male mouse hippocampal CA2 region.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors.

Han QinCenter for Neurointelligence, School of Medicine, Chongqing University, Chongqing 400044, China; Brain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China. Electronic address: qinhan@cqu.edu.cn.
Ling FuBritton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Key Laboratory for Biomedical Photonics of Ministry of Education, School of Engineering Sciences, Huazhong University of Science and Technology, Wuhan 430074, China.
Tingliang JianBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China; Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu 611130, China.
Wenjun JinBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Mengru LiangBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China; Department of Anatomy, School of Basic Medical Sciences, Anhui Medical University, Hefei 230032, China.
Jin LiBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Qianwei ChenBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Xinyu YangCenter for Neurointelligence, School of Medicine, Chongqing University, Chongqing 400044, China.
Haoran DuCenter for Neurointelligence, School of Medicine, Chongqing University, Chongqing 400044, China.
Xiang LiaoCenter for Neurointelligence, School of Medicine, Chongqing University, Chongqing 400044, China.
Kuan ZhangBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Rui WangBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Shanshan LiangBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China.
Jiwei YaoCenter for Neurointelligence, School of Medicine, Chongqing University, Chongqing 400044, China.
Bo HuInstitute of Brain and Intelligence, Third Military Medical University, Chongqing 400038, China.
Shuancheng RenInstitute of Brain and Intelligence, Third Military Medical University, Chongqing 400038, China.
Chunqing ZhangInstitute of Brain and Intelligence, Third Military Medical University, Chongqing 400038, China.
Yanjiang WangInstitute of Brain and Intelligence, Third Military Medical University, Chongqing 400038, China.
Zhian HuInstitute of Brain and Intelligence, Third Military Medical University, Chongqing 400038, China.
Hongbo JiaAdvanced Institute for Brain and Intelligence, Guangxi University, Nanning 530004, China; Institute of Neuroscience and the Munich Cluster for Systems Neurology, Technical University of Munich, 80802 Munich, Germany; Brain Research Instrument Innovation Center, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou 215163, China; Combinatorial NeuroImaging Core Facility, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany.
Arthur KonnerthAdvanced Institute for Brain and Intelligence, Guangxi University, Nanning 530004, China; Institute of Neuroscience and the Munich Cluster for Systems Neurology, Technical University of Munich, 80802 Munich, Germany.
Xiaowei ChenBrain Research Center and State Key Laboratory of Trauma, Burns, and Combined Injury, Third Military Medical University, Chongqing 400038, China; Chongqing Institute for Brain and Intelligence, Guangyang Bay Laboratory, Chongqing 400064, China. Electronic address: xiaowei_chen@tmmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hippocampal CA2 region plays a key role in social memory. The encoding of such memory involves afferent activity from the hypothalamic supramammillary nucleus (SuM) to CA2. However, the neuronal circuits required for consolidation of freshly encoded social memory remain unknown. Here, we used circuit-specific optical and single-cell electrophysiological recordings in mice to explore the role of sleep in social memory consolidation and its underlying circuit mechanism. We found that SuM neurons projecting to CA2 were highly active during rapid-eye-movement (REM) sleep but not during non-REM sleep or quiet wakefulness. REM-sleep-selective optogenetic silencing of these neurons impaired social memory. By contrast, the silencing of another group of REM sleep-active SuM neurons that projects to the dentate gyrus had no effect on social memory. Therefore, we provide causal evidence that the REM sleep-active hypothalamic neurons that project to CA2 are specifically required for the consolidation of social memory.

Indexed as

Memory ConsolidationAnimalsMiceSleephippocampal CA2hypothalamusmemory consolidationrapid-eye-movement sleepsocial memoryspatial memorysupramammillary nucleus

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.