Evidence map›Paper›PMID 39165716›Full record

ArticleFrontiers in molecular neuroscience2024

Induction of seizures and initiation of epileptogenesis by pilocarpine in zebrafish larvae.

Kinga Gawel, Monika Hulas-Stasiak, Marta Marszalek-Grabska, Anna Grenda, Aleksandra Siekierska, Nataliia Kosheva, Wietske van der Ent, Camila V Esguerra, Pawel Krawczyk, Waldemar A Turski

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

10 authors.

Kinga GawelDepartment of Experimental and Clinical Pharmacology, Medical University of Lublin, Lublin, Poland.
Monika Hulas-StasiakDepartment of Functional Anatomy and Cytobiology, Maria Curie-Sklodowska University, Lublin, Poland.
Marta Marszalek-GrabskaDepartment of Experimental and Clinical Pharmacology, Medical University of Lublin, Lublin, Poland.
Anna GrendaDepartment of Pneumology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Aleksandra SiekierskaVirusBank Platform, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Nataliia KoshevaDepartment of Experimental and Clinical Pharmacology, Medical University of Lublin, Lublin, Poland.
Wietske van der EntChemical Neuroscience Group, Centre for Molecular Medicine Norway, University of Oslo, Forskningsparken, Oslo, Norway.
Camila V EsguerraChemical Neuroscience Group, Centre for Molecular Medicine Norway, University of Oslo, Forskningsparken, Oslo, Norway.
Pawel KrawczykDepartment of Pneumology, Oncology and Allergology, Medical University of Lublin, Lublin, Poland.
Waldemar A TurskiDepartment of Experimental and Clinical Pharmacology, Medical University of Lublin, Lublin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Preclinical models of seizures and epilepsy in rodents contributed substantially to the discovery of currently available antiseizure medications. These were also broadly used for investigation of processes of epileptogenesis. Nevertheless, rodent models pose some limitations, thus, new models using alternative species are in high demand. The aim of this study was to describe a new model of seizures/epilepsy induced by the cholinomimetic agent, pilocarpine (PILO), in larval zebrafish. Methods: Local field potential (LFP) recordings were conducted to analyze electroencephalographic discharges and correlate it with larval behavior. Hematoxylin and eosin (H&E) staining, as well as TUNEL staining were performed to analyze morphology and apoptosis, respectively. Real-time quantitative polymerase chain reaction (qRT-PCR) was undertaken for gene expression analysis. Results: Acute exposure to PILO, in a concentration-dependent manner, induces electroencephalographic discharges in larval zebrafish, which behaviorally manifest as decreased locomotion and moving time, but enhanced movement velocity. The PILO-induced seizure-like activity is behaviorally distinct from this induced by the application of chemoconvulsant pentylenetetrazole (PTZ). Zebrafish larvae previously exposed to PILO (2 h), after a washing out period, exhibit spontaneous, unprovoked discharges and apoptotic changes in their brains. Significance: Here, we comprehensively investigated a new model of PILO-induced seizures/epilepsy in larval zebrafish. We propose that this model may be used to study epileptogenesis and for antiseizure drug screening purposes.

Indexed as

epileptogenesislocal field potential recordingslocomotor activitypilocarpineseizurezebrafish

Identifiers

PMID39165716
PMCPMC11333333

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