Evidence map›Paper›PMID 33883658›Full record

ArticleScientific reports2021

Behavioral characteristics as potential biomarkers of the development and phenotype of epilepsy in a rat model of temporal lobe epilepsy.

Karolina Nizinska, Kinga Szydlowska, Avgoustinos Vouros, Anna Kiryk, Aleksandra Stepniak, Eleni Vasilaki, Katarzyna Lukasiuk

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

14 citing papers in PubMed, 26 citations in OpenAlex.

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  11. Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
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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 at 2 institutions in 2 countries.

Karolina NizinskaLaboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland. k.nizinska@nencki.edu.pl.
Kinga SzydlowskaLaboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland.
Avgoustinos VourosDepartment of Computer Science, Faculty of Engineering, University of Sheffield, Sheffield, Great Britain.
Anna KirykLaboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland.
Aleksandra StepniakLaboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland.
Eleni VasilakiDepartment of Computer Science, Faculty of Engineering, University of Sheffield, Sheffield, Great Britain.
Katarzyna LukasiukLaboratory of Epileptogenesis, Nencki Institute of Experimental Biology, Warsaw, Poland.
Instytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study performed a detailed analysis of behavior in a rat model of epilepsy using both established and novel methodologies to identify behavioral impairments that may differentiate between animals with a short versus long latency to spontaneous seizures and animals with a low versus high number of seizures. Temporal lobe epilepsy was induced by electrical stimulation of the amygdala. Rats were stimulated for 25 min with 100-ms trains of 1-ms biphasic square-wave pluses that were delivered every 0.5 s. Electroencephalographic recordings were performed to classify rats into groups with a short latency (< 20 days, n = 7) and long latency (> 20 days, n = 8) to the first spontaneous seizure and into groups with a low number of seizures (62 ± 64.5, n = 8) and high number of seizures (456 ± 185, n = 7). To examine behavioral impairments, we applied the following behavioral tests during early and late stages of epilepsy: behavioral hyperexcitability, open field, novel object exploration, elevated plus maze, and Morris water maze. No differences in stress levels (e.g., touch response in the behavioral hyperexcitability test), activity (e.g., number of entries into the open arms of the elevated plus maze), or learning (e.g., latency to find the platform in the Morris water maze test during training days) were observed between animals with a short versus long latency to develop spontaneous seizures or between animals with a low versus high number of seizures. However, we found a higher motor activity measured by higher number of entries into the closed arms of the elevated plus maze at week 26 post-stimulation in animals with a high number of seizures compared with animals with a low number of seizures. The analysis of the Morris water maze data categorized the strategies that the animals used to locate the platform showing that the intensity of epilepsy and duration of epileptogenesis influenced swimming strategies. These findings indicate that behavioral impairments were relatively mild in the present model, but some learning strategies may be useful biomarkers in preclinical studies.

Indexed as

Behavior, AnimalAnimalsBiomarkersDisease Models, AnimalElectroencephalographyEpilepsy, Temporal LobeExploratory BehaviorMaleMorris Water Maze TestOpen Field TestPhenotypeRatsRats, Sprague-DawleySeizuresBiomarkers

Identifiers

PMID33883658
PMCPMC8060252
OpenAlexW3153943348

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.