Evidence map›Paper›PMID 40072098›Full record

ArticleCells2025

THz Waves Improve Spatial Working Memory by Increasing the Activity of Glutamatergic Neurons in Mice.

Lequan Song, Zhiwei He, Ji Dong, Haoyu Wang, Jing Zhang, Binwei Yao, Xinping Xu, Hui Wang, Li Zhao, Ruiyun Peng

Abstract read
In one paragraph

Article in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Lequan SongBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Zhiwei HeBeijing Institute of Radiation Medicine, 100850 Beijing, China.ORCID 0000-0002-1197-1203
Ji DongBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Haoyu WangBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Jing ZhangBeijing Institute of Radiation Medicine, 100850 Beijing, China.ORCID 0000-0002-6677-3941
Binwei YaoBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Xinping XuBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Hui WangBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Li ZhaoBeijing Institute of Radiation Medicine, 100850 Beijing, China.
Ruiyun PengBeijing Institute of Radiation Medicine, 100850 Beijing, China.

Funding

National Natural Science Foundation of China U2130104
6 · The paper itself

Abstract

Terahertz (THz) waves, a novel type of radiation with quantum and electronic properties, have attracted increasing attention for their effects on the nervous system. Spatial working memory, a critical component of higher cognitive function, is coordinated by brain regions such as the infralimbic cortex (IL) region of the medial prefrontal cortex and the ventral cornu ammonis 1 (vCA1) of hippocampus. However, the regulatory effects of THz waves on spatial working memory and the underlying mechanisms remain unclear. In this study, the effects of 0.152 THz waves on glutamatergic neuronal activity and spatial working memory and the related mechanisms were investigated in cell, brain slice, and mouse models. Cellular experiments revealed that THz waves exposure for 60 min significantly increased the intrinsic excitability of primary hippocampal neurons, enhanced glutamatergic neuron activity, and upregulated the expression of molecules involved in glutamate metabolism. In brain slice experiments, THz waves markedly elevated neuronal activity, promoted synaptic plasticity, and increased glutamatergic synaptic transmission within the IL and vCA1 regions. Molecular dynamics simulations found that THz waves could inhibit the ion transport function of glutamate receptors. Moreover, Y-maze tests demonstrated that mice exposed to THz waves exhibited significantly improved spatial working memory. Multiomics analyses indicated that THz waves could induce changes in chromatin accessibility and increase the proportion of excitatory neurons. These findings suggested that exposure to 0.152 THz waves increased glutamatergic neuronal activity, promoted synaptic plasticity, and improved spatial working memory, potentially through modifications in chromatin accessibility and excitatory neuron proportions.

Indexed as

Glutamic AcidMemory, Short-TermNeuronsSpatial MemoryTerahertz RadiationAnimalsHippocampusMaleMaze LearningMiceMice, Inbred C57BLNeuronal PlasticityGlutamic Acidglutamatergic neuronsmultiomicssynaptic plasticitysynaptic transmissionterahertz wavesworking memory

Identifiers

PMID40072098
PMCPMC11898596

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.