Evidence map›Paper›PMID 41432569›Full record

ArticleEpilepsia2026

Synchrotron-generated microbeams as a radiosurgical alternative for drug-resistant epilepsies: Proof of concept in a mouse model of mesiotemporal lobe epilepsy.

Loan Samalens, Camille Beets, Clothilde Courivaud, Sarvenaz Keshmiri, Jean-François Adam, Paolo Pellicioli, Emmanuel Luc Barbier, Raphaël Serduc, Antoine Depaulis

Abstract read
In one paragraph

Article in Epilepsia, 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

9 authors.

Loan SamalensU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0000-0002-3596-231X
Camille BeetsU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0009-0000-8440-3007
Clothilde CourivaudU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0000-0002-2826-0192
Sarvenaz KeshmiriU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0000-0002-1810-4217
Jean-François AdamSynchrotron Radiation for Biomedecine (STROBE), Inserm UA7, Saint Martin d'Hères, France.ORCID https://orcid.org/0000-0001-5608-3616
Paolo PellicioliEuropean Synchrotron Radiation Facility (ESRF), Grenoble, France.ORCID https://orcid.org/0000-0003-3590-116X
Emmanuel Luc BarbierU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0000-0002-4952-1240
Raphaël SerducSynchrotron Radiation for Biomedecine (STROBE), Inserm UA7, Saint Martin d'Hères, France.ORCID https://orcid.org/0000-0003-3294-8544
Antoine DepaulisU1216, Grenoble Institut Neurosciences, Université Grenoble Alpes, Inserm, Grenoble, France.ORCID https://orcid.org/0000-0001-6543-6700

Funding

Agence Nationale de la Recherche ANR-20-CE17-0025-01
6 · The paper itself

Abstract

objectiveOne-third of patients with epilepsy, particularly those with mesial temporal lobe epilepsy (MTLE), remain resistant to medication. Resective surgery, the gold standard, is highly invasive and carries significant risks. Here, using a mouse model, we explored the potential of microbeam radiation therapy (MRT), a new technique based on the spatial microfractionation of high-flux X-rays, as a non-invasive alternative for treating MTLE.

methodsMTLE was modeled in male C57BL6/J mice via unilateral kainate injection in the dorsal hippocampus. Mice with magnetic resonance imaging (MRI)-validated hippocampal sclerosis (HS) were irradiated at the European Synchrotron Radiation Facility (ESRF) using MRT with either a single trajectory (peak doses = 125-500 Gy) or multiple trajectories (2 or 5 ports at a cumulated peak dose of 125 Gy at the target). Their focal seizures were then monitored with use of electroencephalography (EEG) during 8 weeks, upon which immunochemistry was performed to assess potential tissular toxicity.

resultsAnteroposterior 1-port MRT significantly reduced EEG-recorded focal seizures at 125 and 250 Gy, in a dose-dependent manner. However, increased mortality was observed at 500 Gy. Immunohistolabeling revealed neuronal loss (revealed by NeuN staining), microgliosis (revealed by Iba1 straining), and astrogliosis (revealed by GFAP staining) limited to the microbeam tracks at all doses in the injected hippocampus and adjacent brain structures (e.g., cortex). Five-port MRT with a peak dose of 125 Gy at the target improved the antiepileptic effect, whereas no significant tissue alterations outside the microbeam tracks were detected by histological assessment. SIGNIFICANCE: This proof-of-concept study highlights MRT as a promising non-invasive therapy for drug-resistant focal epilepsies with optimal peak doses of 125-250 Gy, and it suggests that distributing the dose through multiple angles optimizes the therapeutic effect. MRT could provide a safer alternative to surgery, warranting further investigations.

Indexed as

Drug Resistant EpilepsyEpilepsy, Temporal LobeRadiosurgerySynchrotronsAnimalsDisease Models, AnimalElectroencephalographyHippocampusKainic AcidMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLProof of Concept StudySclerosisKainic Acidepilepsyhippocampusmouse modelradiotherapyX‐ray

Identifiers

PMID41432569
PMCPMC13075611

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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.