Evidence map›Paper›PMID 41278939›Full record

ArticlebioRxiv : the preprint server for biology2025

Behavioral unresponsiveness and impaired auditory event-related potentials in the anterior insula during rat absence seizures.

Stefan Sumsky, Rory Ashmeade, Jiayang Liu, Yang Zheng, Samiksha Chopra, Ben F Gruenbaum, Cian McCafferty, Hal Blumenfeld

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

8 authors.

Stefan SumskyDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.ORCID 0000-0002-9450-5004
Rory AshmeadeDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.
Jiayang LiuDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.
Yang ZhengDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.
Samiksha ChopraDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.ORCID 0000-0003-3458-3219
Ben F GruenbaumDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.ORCID 0000-0002-3120-5709
Cian McCaffertyDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.ORCID 0000-0001-5206-4450
Hal BlumenfeldDepartment of Neurology, Yale University School of Medicine, 333 Cedar Street, New Haven, Connecticut 06520, USA.ORCID 0000-0003-0812-8132

Funding

Remote effects of focal hippocampal seizures on neocortical functionR01NS066974 · NINDS · YALE UNIVERSITY · PI HAL BLUMENFELD · 2011 to 2026
$5.5M
Neuroimaging, neuronal firing and behavior in spike-wave seizuresR37NS100901 · NINDS · YALE UNIVERSITY · PI BLUMENFELD, HAL · 2017 to 2023
$3.0M
NINDS NIH HHS R01 NS066974NINDS NIH HHS R37 NS100901
6 · The paper itself

Abstract

Absence epilepsy is marked by sudden lapses in consciousness accompanied by spike-wave discharges (SWDs), yet the neural mechanisms underlying impaired sensorimotor processing in these episodes remain unresolved. Prior work has shown that normal-appearing signals can persist in primary sensory cortical areas during seizures, suggesting that impaired behavioral responsiveness may arise from disruptions in higher-order association cortex. To investigate this hypothesis, we combined behavioral testing with simultaneous local field potential recordings in Genetic Absence Epilepsy Rats from Strasbourg (GAERS). Rats were trained in an auditory conditioned response task, allowing comparison of tone-evoked responses during interictal baseline and ictal SWDs. We found that behavioral performance collapsed during SWDs, with correct responses falling from ~88% at baseline to <1% during SWDs (p < 0.001). Nevertheless, auditory event-related potentials in primary auditory cortex (Au1) during SWDs were not significantly decreased. In contrast, we identified a novel oscillatory evoked potential in the anterior insular cortex (AIC) that was robust in controls, attenuated in GAERS at baseline, and markedly reduced during SWDs. Notably, reductions in AIC response magnitude also occurred during satiated, unmotivated states, but waveform structure was preserved, distinguishing motivational modulation from seizure-related disruption. These results demonstrate that absence seizures selectively impair signals in the anterior insula rather than in primary auditory cortex, identifying the AIC as a potentially critical hub for gating auditory conscious awareness. Beyond refining models of seizure-related unconsciousness, the discovery of an insular oscillatory potential highlights a candidate biomarker and intervention target for absence epilepsy, with broader implications for understanding impaired consciousness in anesthesia, sleep, and brain injury.

Indexed as

absence epilepsyanterior insulaConsciousnesscortexelectroencephalography (EEG)Genetic absence epilepsy rats of Strasbourg (GAERS)seizuressensorimotor processing

Identifiers

PMID41278939
PMCPMC12632520

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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.