Evidence map›Paper›PMID 41439706›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Synchrony of neuromodulatory systems during NREM sleep.

Sasa Teng, Angie N Maldonado Rodriguez, Ruizhi Wang, Xinyue Chen, Yueqing Peng

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. A molecular integrator of sleep duration and interruption.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Sasa TengDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032.
Angie N Maldonado RodriguezDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032.ORCID 0009-0009-3277-1858
Ruizhi WangDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032.ORCID 0009-0008-8976-8230
Xinyue ChenDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032.ORCID 0000-0003-0264-1488
Yueqing PengDepartment of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY 10032.ORCID 0000-0002-3488-0670

Funding

Neural Control of NREM Sleep in the MedullaR01NS129997 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Yueqing Peng · 2023 to 2026
$1.6M
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS129997NINDS NIH HHS R01 NS129997
6 · The paper itself

Abstract

Neuromodulatory systems play an essential role in regulating brain states and functions. The canonical view is that the release of monoamines including norepinephrine (NE) and serotonin (5-HT) is high during wakefulness and attenuated during sleep, particularly during rapid eye movement (REM) sleep, whereas the cholinergic system is active during both wakefulness and REM sleep and quiescent during non-REM (NREM) sleep. Recent studies have revealed a slow and rhythmic release pattern of neuromodulators during NREM sleep that drives infraslow oscillation (ISO) (0.02 to 0.03 Hz) in the brain. A key question is whether/how the release of different neuromodulators during sleep is coordinated. In this study, we combined 2-site fiber photometry with electroencephalogram/electromyography recording to monitor the release of NE, 5-HT, and acetylcholine in the cortex and hippocampus during sleep and wake cycles. We found that the ISO of these neuromodulators is synchronized during NREM sleep. The synchrony between neuromodulatory systems increases in the oscillatory cycles leading to arousal. Furthermore, pharmacological inhibition of either the 5-HT or NE system eliminates the oscillation of other neuromodulators during NREM sleep. Optogenetic activation of 5-HT or NE neurons during NREM sleep induces the release of other neuromodulators in the absence of sleep-to-wake transitions. These results suggest that the rhythmic neuromodulator releases are highly coordinated in the brain. The synchrony among multiple neuromodulatory systems across brain regions provides a powerful neural mechanism to orchestrate sleep architecture and sleep-related neural processes.

Indexed as

Neurotransmitter AgentsSleep, Slow-WaveAcetylcholineAnimalsElectroencephalographyElectromyographyHippocampusMaleMiceNorepinephrineOptogeneticsSerotoninSleep, REMWakefulnessAcetylcholineNeurotransmitter AgentsNorepinephrineSerotonininfraslow oscillationneuromodulatornorepinephrineNREM sleepserotonin

Identifiers

PMID41439706
PMCPMC12772183

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.