Evidence map›Paper›PMID 42014476›Full record

ArticleCommunications medicine2026

Non-vectorial integration of intersectional short-pulse stimulation enables enhanced deep brain modulation and effective seizure control.

Tamás Földi, Miklos Szoboszlay, Zoltán Chadaide, Bence Radics, Bálint Horváth, Endre Vecsernyés, István Langó, Péter Ráfi, Andrea Pejin, Lívia Barcsai and 10 more

Abstract read
In one paragraph

Article in Communications medicine, 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

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

20 authors.

Tamás Földi *MTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0001-8364-508X
Miklos Szoboszlay *Neunos ZRt, Szeged, Hungary.ORCID http://orcid.org/0000-0001-5736-2967
Zoltán ChadaideMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.
Bence RadicsDepartment of Pathology, University of Szeged, Szeged, Hungary.
Bálint HorváthNeunos ZRt, Szeged, Hungary.ORCID http://orcid.org/0009-0004-6913-6667
Endre VecsernyésNeunos ZRt, Szeged, Hungary.
István LangóNeunos ZRt, Szeged, Hungary.
Péter RáfiMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.
Andrea PejinMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.
Lívia BarcsaiMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0002-5646-8265
Gábor KozákMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0002-3473-9351
Nóra ForgóMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.
Kristóf FuruglyásNeunos ZRt, Szeged, Hungary.
Olivér NagyDepartment of Physiology, Anatomy and Neuroscience, Faculty of Sciences University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0002-6599-6799
Anett J NagyMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.
Tamás LaszlovszkyNeunos ZRt, Szeged, Hungary.
Zoltán SomogyváriNeunos ZRt, Szeged, Hungary.
Magor L LőrinczMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0001-5240-1904
Orrin DevinskyDepartment of Neurology, NYU Langone Comprehensive Epilepsy Center, NYU Grossman School of Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0003-0044-4632
Antal BerényiMTA-SZTE 'Momentum' Oscillatory Neuronal Networks Research Group, Department of Physiology, University of Szeged, Szeged, Hungary. drberenyi@gmail.com.ORCID http://orcid.org/0000-0003-0084-8530

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTranscranial electrical stimulation (TES) has limited spatial focus and depth penetration, constraining its therapeutic efficacy. Intersectional Short-Pulse (ISP) stimulation was developed to overcome these limitations by delivering rapidly switching pulses that can be temporally integrated by neuronal membranes. Here, we aimed to establish the biophysical basis of ISP-induced temporal summation and to test whether this mechanism enables effective brain modulation in vivo.

methodsWe combined finite-element modeling, cadaver measurements (n = 2 human cadavers), and biophysically realistic NEURON simulations to characterize the spatial and temporal properties of ISP-induced electric fields. In vivo whole-cell patch-clamp recordings were performed in the rat somatosensory cortex (female Wistar rat) to test the membrane-level integration of sequential electric field pulses. Functional efficacy was evaluated using closed-loop ISP stimulation in a hippocampal kindling model of temporal lobe epilepsy in male Long-Evans rats (n = 11 animals, >500 induced seizures analyzed across conditions).

resultsHere we show that neurons integrate sequential ISP pulses in a non-vectorial, temporally accumulative manner, consistent with membrane-level charge integration rather than extracellular field superposition. ISP and conventional TES simulations produced similar instantaneous field magnitudes, but ISP stimulation resulted in more uniform neuronal excitability across brain depths. Closed-loop ISP stimulation significantly outperformed conventional TES in reducing seizure duration and severity. ISP reduced hippocampal seizure duration by 45% and 35% compared to SHAM stimulation and conventional TES, and significantly reduced motor seizure severity.

conclusionsISP stimulation provides a non-invasive neuromodulation approach that enhances deep brain engagement through rapid, temporally structured pulse sequences. These findings demonstrate effective seizure suppression in a rodent model and support the translational potential of ISP for disorders involving pathological neural dynamics.

Identifiers

PMID42014476
PMCPMC13287739

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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.