Evidence map›Paper›PMID 42243171›Full record

ArticleScientific reports2026

Kainic acid pig model of hippocampal epilepsy.

Filip Mivalt, Daniela Maltais, Inyong Kim, Jiwon Kim, Patrik Began, Andrea Duque Lopez, Veronika Krakorova, Bailey Winter, Cheng Yen Kuo, Shelja Sharma and 11 more

Abstract read
In one paragraph

Article in Scientific reports, 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

21 authors.

Filip Mivalt *Department of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA. mivalt.filip@mayo.edu.
Daniela Maltais *Department of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Inyong KimDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Jiwon KimDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Patrik BeganDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Andrea Duque LopezDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Veronika KrakorovaDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Bailey WinterDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Cheng Yen KuoDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Shelja SharmaDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Elizabeth S HartyDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Luke H KimDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Nicholas GreggDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Daniel R MontonyeDepartment of Comparative Medicine, Mayo Clinic, Rochester, MN, USA.
Christopher K GowDepartment of Comparative Medicine, Mayo Clinic, Rochester, MN, USA.
Kai J MillerDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.
Jamie Van GompelDepartment of Neurologic Surgery, Mayo Clinic, Rochester, MN, USA.
Kent LeydeCadence Neuroscience Inc., Seattle, WA, USA.
Vaclav KremenDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Su-Youne ChangDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA.
Gregory A WorrellDepartment of Neurology, BNEL (Bioelectronics Neurophysiology & Engineering Lab), Mayo Clinic, Rochester, MN, USA. worrell.gregory@mayo.edu.

Funding

Reliable Seizure Prediction Using Physiological Signals and Machine LearningR01NS092882 · NINDS · MAYO CLINIC ROCHESTER · PI Gregory A Worrell · 2015 to 2026
$5.7M
Cadence Neuroscience Provided devicesCadence Neuroscience Salary SupportNINDS NIH HHS R01 NS092882NINDS NIH HHS R01-NS092882
6 · The paper itself

Abstract

Translational large-animal models that can accommodate human-scale implantable devices are essential for advancing neuromodulation therapies in epilepsy. This study establishes a kainic acid (KA)-induced porcine model of mesial temporal lobe epilepsy (mTLE) using clinical imaging, stereotactic surgery, and a fully implantable neural stimulator-recorder (INSR) device designed for humans. Seven pigs (six KA-treated and one saline control) underwent MRI-guided stereotactic implantation of electrodes targeting bilateral hippocampus (HPC) and anterior thalamus (ANT), followed by intra-hippocampal KA or saline infusion. Local field potentials (LFP) were recorded continuously with synchronized video monitoring. Seizures and LFP interictal epileptiform-like discharges (IEDs) were quantified using validated automated detectors. Histology was performed in the saline control and the longest surviving KA-treated pig. Intra-hippocampal KA infusion induced acute status epilepticus in all treated pigs (6/6). Four animals survived to chronic monitoring with spontaneous seizures observed in three pigs (2,733 seizures; mean duration of 27.2 ± 17.6 s). IEDs were observed in bilateral HPC of all animals, including saline control, with higher rates in the lesioned HPC (p < 0.0001). While the IED morphology is consistent with epileptiform activity, IEDs alone are not specific for epilepsy and physiological transients (e.g. sharp-wave ripples) and injury-related hyperexcitability or strain-specific hyperexcitability cannot be excluded. Histological analysis revealed patchy neuronal loss and cytoarchitectural changes in HPC. This porcine model reproduces electrophysiological features of human mTLE. This approach provides a powerful translational bridge for developing and testing next-generation INSR and neuromodulation strategies in freely behaving large animals.

Indexed as

EpilepsyEpilepsy, Temporal LobeHippocampusKainic AcidAnimalsDisease Models, AnimalElectroencephalographyFemaleLocal Field Potential MeasurementMagnetic Resonance ImagingSeizuresSwineKainic AcidEpilepsyImplantable neurostimulatorsKainic acidPig

Identifiers

PMID42243171
PMCPMC13478606

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.