Evidence map›Paper›PMID 41600571›Full record

ArticleToxics2025

Persistently Elevated Gamma Power and Delayed Brain Damage in Aged Rats Acutely Exposed to Soman Without Status Epilepticus: Comparisons with Seizing Rats Treated with Midazolam or with Tezampanel and Caramiphen.

Taiza H Figueiredo, Vassiliki Aroniadou-Anderjaska, Marcio De Araujo Furtado, Volodymyr I Pidoplichko, Katia Rossetti, Lucille A Lumley, Maria F M Braga

Abstract read
In one paragraph

Article in Toxics, 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

7 authors.

Taiza H FigueiredoDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Vassiliki Aroniadou-AnderjaskaDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Marcio De Araujo FurtadoDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Volodymyr I PidoplichkoDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Katia RossettiDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Lucille A LumleyU.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, Aberdeen, MD 21010, USA.ORCID 0000-0003-4162-8817
Maria F M BragaDepartment of Anatomy, Physiology, and Genetics, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.

Funding

National Institutes of Health Office of the Director and the U.S. Army Medical Research Institute of Chemical Defense under the oversight of the Chemical Countermeasures Research Program within the Office of Biodefense Research at the National Institutes AOD24006-001 00000NIH HHS 1U01NS123252-01A1
6 · The paper itself

Abstract

Aged animals or humans are more susceptible to permanent brain damage from status epilepticus (SE), making the selection of antiseizure medication even more crucial. This study compared the antiseizure and neuroprotective efficacy of midazolam with that of tezampanel combined with caramiphen in treating soman-induced SE in aged rats. A substantial proportion of soman-exposed aged rats did not develop SE, allowing us to also study this noSE group. SE duration within 24 h post-exposure was significantly longer in the midazolam than the tezampanel + caramiphen group, which was reflected in the EEG power integral. Spectral density analysis showed sustained increase in gamma-band power in the noSE group. Increased delta power in the SE groups lasted longer after midazolam. Body temperature decreased substantially only in the noSE and tezampanel + caramiphen groups. The midazolam group displayed severe neuropathology in the hippocampus and the amygdala 7 days to 6 months post-exposure, whereas the noSE and tezampanel + caramiphen groups exhibited only delayed amygdala damage. Thus, tezampanel + caramiphen has far superior neuroprotective efficacy than midazolam in aged rats. Increased gamma power is associated with seizure resistance; however, even in the absence of SE, delayed neuropathology can develop after a single acute organophosphate exposure.

Indexed as

amygdalacaramiphengamma bandmidazolamnerve agentsorganophosphatesstatus epilepticustezampanel

Identifiers

PMID41600571
PMCPMC12845752

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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.