Evidence map›Paper›PMID 40415257›Full record

ArticleCell proliferation2025

Repetitive Transcranial Magnetic Stimulation Induces Cognitive Recovery in Alzheimer's Disease via GABAergic Neuron Activation of the Cx3cl1-Cx3cr1 Axis.

Yunxiao Kang, Jilun Liu, Yu Wang, Jiaying Wang, Jinyang Wang, Chenming Zhou, Rui Cui, Tianyun Zhang

Abstract read
In one paragraph

Article in Cell proliferation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. 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

8 authors.

Yunxiao KangLaboratory of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Jilun LiuDepartment of Oral and Maxillofacial Surgery, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Yu WangLaboratory of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Jiaying WangLaboratory of Neurobiology, Hebei Medical University, Shijiazhuang, China.
Jinyang WangDepartment of Neurology, The Third Hospital of Hebei Medical University, Shijiazhuang, China.
Chenming ZhouCore Facilities and Centers, Hebei Medical University, Shijiazhuang, China.
Rui CuiNeuroscience Research Center, Hebei Medical University, Shijiazhuang, China.
Tianyun ZhangLaboratory of Neurobiology, Hebei Medical University, Shijiazhuang, China.ORCID https://orcid.org/0009-0009-1900-534X

Funding

Hebei Medical Science Research Project Plan 20221163Hebei Medical Science Research Project Plan 20240255Hebei Medical University Chunyu Project CYCZ2023004Hebei Provincial Natural Science Foundation Precision Medicine Joint Fund Cultivation Project H2025206666Hebei Provincial Natural Science Foundation Precision Medicine Joint Fund Cultivation Project H2025206684Science Research Project of Hebei Education Department QN2024035
6 · The paper itself

Abstract

This study aimed to investigate the impact of repetitive transcranial magnetic stimulation (rTMS) on cognitive recovery in Alzheimer's disease (AD) by exploring the role of GABAergic neuron activation and modulation of the Cx3cl1-Cx3cr1 signalling axis. The 5xFAD mouse model was utilised for scRNA-seq analysis to examine changes in gene expression post-rTMS. Microglial phagocytic activity, amyloid plaque burden, cell-cell communication, microglial morphology and neuroinflammation markers were assessed. Following rTMS, upregulation of Cx3cl1 in GABAergic neurons was observed, leading to enhanced microglial phagocytosis, reduced amyloid plaque burden, improved cell-cell communication, altered microglial morphology and decreased neuroinflammation markers. This study demonstrates that rTMS promotes Aβ clearance and cognitive recovery in AD by activating GABAergic neurons and enhancing Cx3cl1-Cx3cr1 signalling, providing a novel molecular target for non-invasive AD therapy. These findings support the transition from invasive to non-invasive AD treatments, improving patient adherence and therapeutic outcomes. Furthermore, the elucidation of cellular and molecular mechanisms facilitates drug development targeting the Cx3cl1-Cx3cr1 axis, offering new opportunities for AD intervention.

Indexed as

Alzheimer DiseaseChemokine CX3CL1CognitionCX3C Chemokine Receptor 1GABAergic NeuronsTranscranial Magnetic StimulationAmyloid beta-PeptidesAnimalsDisease Models, AnimalHumansMaleMiceMice, TransgenicMicrogliaPlaque, AmyloidSignal TransductionAmyloid beta-PeptidesChemokine CX3CL1CX3C Chemokine Receptor 1Cx3cl1 protein, mouseCx3cr1 protein, mouseAlzheimer's diseasecognitive functionCx3cl1‐Cx3cr1 axisGABAergic neuronsmicrogliarTMS

Identifiers

PMID40415257
PMCPMC12686124

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Registered trials

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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.