Evidence map›Paper›PMID 41878311›Full record

ArticleFrontiers in aging neuroscience2026

Prolonged intermittent theta burst stimulation enhances hippocampal plasticity via GluN2A-mediated signaling.

Danica Popovic, Marina Zaric Kontic, Milica Zeljkovic Jovanovic, Milena Milosevic, Teodora Martic, Tamara Radukic, Andjela Stekic, Emilija Glavonic, Ana Jakovljevic, Katarina Mihajlovic and 3 more

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Danica PopovicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Marina Zaric KonticDepartment of Molecular Biology and Endocrinology, VINČA Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Milica Zeljkovic JovanovicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Milena MilosevicCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Teodora MarticCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Tamara RadukicDepartment of Molecular Biology and Endocrinology, VINČA Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Andjela StekicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Emilija GlavonicDepartment of Molecular Biology and Endocrinology, VINČA Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Ana JakovljevicCenter for Laser Microscopy, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Katarina MihajlovicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Marija Adzic BukvicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.
Ivana StevanovicMedical Faculty of Military Medical Academy, University of Defence, Belgrade, Serbia.
Milorad DragicCenter for Translational Neuroscience, Faculty of Biology, University of Belgrade, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Intermittent theta burst stimulation (iTBS) is increasingly explored as a non-invasive neuromodulatory approach capable of inducing long-lasting plasticity with potential therapeutic value in age-related neurological and psychiatric conditions. However, the cellular and molecular mechanisms underlying iTBS protocols remain largely unknown, limiting its further therapeutic development. Methods: Here, we investigated the behavioral, structural, synaptic, and calcium-dependent effects of a 7-day iTBS600 protocol using a combination of Results: Prolonged iTBS did not alter general locomotor activity, anxiety-like behavior, or short-term recognition memory, indicating preserved baseline behavioral function. Despite the absence of behavioral changes, prolonged iTBS induced robust structural plasticity in hippocampal CA1 neurons, increasing total spine density and selectively enhancing the proportion of thin, learning spines. Synaptosomal analysis revealed upregulation of GluN1 and GluN2A, elevated BDNF levels, and activation of downstream Akt, ERK1/2, and mTOR pathways. Prolonged iTBS also enhanced perineuronal net formation around PV Conclusion: Together, these findings indicate that prolonged iTBS drives coordinated structural, synaptic, and Ca

Indexed as

dendritic spinesGluN2A subunithippocampusiTBSNMDA signalingrepetitive transcranial magnetic stimulationsynaptic plasticity

Identifiers

PMID41878311
PMCPMC13006673

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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.