Evidence map›Paper›PMID 41648455›Full record

ArticlebioRxiv : the preprint server for biology2026

Dose-dependent power and connectivity modulation of low frequency oscillations through transcranial magnetic stimulation in non-human primates.

Malte R Güth, Nipun D Perera, Gary Linn, Kurt Masiello, Brent Butler, Brian E Russ, Charles E Schroeder, Arnaud Falchier, Alexander Opitz

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Malte R GüthDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455.ORCID 0000-0001-7374-9870
Nipun D PereraDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455.ORCID 0000-0002-8173-4529
Gary LinnTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Kurt MasielloTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Brent ButlerTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Brian E RussTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Charles E SchroederTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Arnaud FalchierTranslational Neuroscience Lab Division, Center, Center for Biomedical Imaging and Neuromodulation, Nathan S. Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Alexander OpitzDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota 55455.

Funding

Investigating the molecular, cellular and circuit effects of transcranial magnetic stimulationR01NS109498 · NINDS · UNIVERSITY OF MINNESOTA · PI FALCHIER, ARNAUD Y, OPITZ, ALEXANDER · 2019 to 2022
$3.2M
Validation of Closed-Loop Prefrontal Transcranial Magnetic Stimulation in a Non-Human Primate ModelR01MH136053 · NIMH · UNIVERSITY OF MINNESOTA · PI Arnaud Y Falchier, Alexander Opitz · 2024 to 2026
$2.4M
NIMH NIH HHS R01 MH136053NINDS NIH HHS R01 NS109498
6 · The paper itself

Abstract

Transcranial magnetic stimulation (TMS) is a powerful non-invasive tool for safely modulating neural activity in humans. In particular, the left dorsolateral prefrontal cortex (DLPFC) is a common target site for clinical interventions in disorders such as treatment-resistant depression. Yet, clinical trials investigating the efficacy of TMS often lack neural markers of target engagement of the DLPFC. Local field potentials (LFPs), such as prefrontal theta oscillations, have been implicated in the clinical symptoms of these disorders. However, non-invasive electroencephalography (EEG) recordings in humans are limited by their spatial resolution and challenges of interpreting EEG signals. In this study, we investigate the effects of single-pulse TMS applied to the left prefrontal cortex in non-human primates on LFPs recorded through intracranial EEG. Compared to sham TMS, the intensity of active TMS pulses scaled with LFP power changes in a 1-13 Hz range at contacts close to the stimulation site in the prefrontal cortex (e.g., caudate nucleus, anterior cingulate cortex, insular cortex) as well as contacts that were more distal (e.g., posterior cingulate cortex, temporal lobe). To test how TMS modulates connectivity between these regions, we conducted a phase-based connectivity analysis. TMS pulses initially enhanced and then disrupted connectivity at 1-13 Hz between the stimulation site and other contacts. Connectivity rebounded approximately 1500 ms post-stimulation. Only the initial enhancement in connectivity scaled with TMS intensity. Our results demonstrate a dose-dependent power modulation of low frequency LFPs across prefrontal, parietal and temporal cortical regions by single pulses. Furthermore, they show that TMS applied over the left prefrontal cortex can enhance and interrupt short- and long-range connectivity. Our study advances the understanding of the effects of TMS on brain oscillations and connectivity with direct relevance for clinical applications in neuromodulation therapies.

Identifiers

PMID41648455
PMCPMC12871326

What Socratic holds

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LicenceCC BY
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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 Socratic graph.