Evidence map›Paper›PMID 39887927›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Temporal Association Cortex Gates Sound-Evoked Arousal from NREM Sleep.

Haipeng Yu, Jincheng Wang, Ruiqi Pang, Penghui Chen, Tiantian Luo, Xuan Zhang, Yatao Liao, Chao Hu, Miaoqing Gu, Bingmin Luo and 11 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Temporal Association Cortex Gates Sound-Evoked Arousal from NREM Sleep.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. Review
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

21 authors.

Haipeng YuAdvanced Institute for Brain and Intelligence, School of Physical Science and Technology, Guangxi University, Nanning, 530004, China.
Jincheng WangDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Ruiqi PangGuangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning, 530004, China.
Penghui ChenDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Tiantian LuoDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Xuan ZhangDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Yatao LiaoDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Chao HuDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Miaoqing GuAdvanced Institute for Brain and Intelligence, School of Physical Science and Technology, Guangxi University, Nanning, 530004, China.
Bingmin LuoDepartment of Neurosciences, Case Western Reserve University School of Medicine, Cleveland, OH, 44106, USA.
Zhiyue ShiDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Mengyao LiGuangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning, 530004, China.
Yueting ZhangGuangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning, 530004, China.
Qiaoqian WeiGuangxi Key Laboratory of Special Biomedicine, School of Medicine, Guangxi University, Nanning, 530004, China.
Wei YuanDepartment of Otolaryngology, Chongqing General Hospital, Chongqing University, Chongqing, 400038, China.
Hui XieSchool of Architecture and Urban Planning, Chongqing University, Chongqing, 400044, China.
Zhiyi ChenExperimental Research Center for Medical and Psychological Science, School of Psychology, Army Medical University, Chongqing, 400038, China.
Hongbang LiuAdvanced Institute for Brain and Intelligence, School of Physical Science and Technology, Guangxi University, Nanning, 530004, China.
Shuancheng RenDepartment of Physiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Xiaowei ChenBrain Research Center and State Key Laboratory of Trauma and Chemical Poisoning, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.
Yi ZhouDepartment of Neurobiology, College of Basic Medicine, Army Medical University, Chongqing, 400038, China.ORCID https://orcid.org/0000-0002-2623-8960

Funding

Guangxi Science and Technology Base & Talents Fund GUIKE AD22035948National Major Science and Technology Projects of China 2022ZD0205600National Natural Science Foundation of China 32171050 to YZNational Natural Science Foundation of China 32371001
6 · The paper itself

Abstract

Sound-evoked wakefulness from sleep is crucial in daily life, yet its neural mechanisms remain poorly understood. It is found that CaMKIIα+ neurons in the temporal association cortex (TeA) of mice are not essential for natural awakening from sleep. However, optogenetic activation of these neurons reliably induces wakefulness from non-rapid eye movement (NREM) sleep but not from rapid eye movement (REM) sleep. In vivo electrophysiological and calcium recordings further demonstrated that TeA neurons are monotonically tuned to sound intensity but not frequency. More importantly, it is found that the activity of CaMKIIα+ neurons in TeA can gate sound-evoked arousal from NREM sleep, which is further confirmed by optogenetic manipulations. Further investigation reveals that the baseline excitability of TeA CaMKIIα+ neurons and the delta oscillations in the electroencephalogram are particularly important in regulating the evoked activity of TeA neurons. Anatomical and functional screening of downstream targets of TeA reveals that excitatory projections from TeA glutamatergic neurons to glutamatergic neurons in the basolateral/lateral amygdala are critical for modulating sound-evoked arousal from NREM sleep. These findings uncover a top-down regulatory circuit that selectively governs sound-evoked arousal from NREM sleep, with the TeA functioning as a key connecting cortex to subcortical regions.

Indexed as

ArousalSleep, Slow-WaveAnimalsElectroencephalographyMaleMiceMice, Inbred C57BLNeuronsOptogeneticsSleepWakefulnessarousalbasolateral amygdalalateral amygdalaNREM sleepsoundtemporal association cortex

Identifiers

PMID39887927
PMCPMC11948000

What Socratic holds

Textmetadata
LicenceCC BY
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.