Evidence map›Paper›PMID 37129175›Full record

ArticleJournal of neurochemistry2024

Characterisation and automated quantification of induced seizure-related behaviours in Xenopus laevis tadpoles.

Sandesh Panthi, Phoebe A Chapman, Paul Szyszka, Caroline W Beck

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Assessing circuit function in the developingFrontiers in behavioral neuroscience · 2026
    Review
  2. Automated Behavioral Tracking and Analysis of Xenopus Tadpoles.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
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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

4 authors at 2 institutions in 1 country.

Sandesh PanthiDepartment of Zoology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-2363-0895
Phoebe A ChapmanDepartment of Zoology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-3303-9134
Paul SzyszkaDepartment of Zoology, University of Otago, Dunedin, New Zealand.ORCID 0000-0003-2043-6656
Caroline W BeckDepartment of Zoology, University of Otago, Dunedin, New Zealand.ORCID 0000-0001-6489-7425
Brain Research New Zealand · NZUniversity of Otago · NZ

Funding

Neurological Foundation of New Zealand 2025-PRG
6 · The paper itself

Abstract

Epilepsy, a clinical diagnosis characterised by paroxysmal episodes known as seizures, affects 1% of people worldwide. Safe and patient-specific treatment is vital and can be achieved by the development of rapid pre-clinical models of for identified epilepsy genes. Epilepsy can result from either brain injury or gene mutations, and can also be induced chemically. Xenopus laevis tadpoles could be a useful model for confirmation of variants of unknown significance found in epilepsy patients, and for drug re-purposing screens that could eventually lead to benefits for patients. Here, we characterise and quantify seizure-related behaviours in X. laevis tadpoles arrayed in 24-well plates. To provoke acute seizure behaviours, tadpoles were chemically induced with either pentylenetetrazole (PTZ) or 4-aminopyridine (4-AP). To test the capacity to adapt this method for drug testing, we also exposed induced tadpoles to the anti-seizure drug valproate (VPA). Four induced seizure-like behaviours were described and manually quantified, and two of these (darting, circling) could be accurately detected automatically, using the video analysis software TopScan. Additionally, we recorded swimming trajectories and mean swimming velocity. Automatic detection showed that either PTZ or 4-AP induced darting behaviour and increased mean swimming velocity compared to untreated controls. Both parameters were significantly reduced in the presence of VPA. In particular, darting behaviour was a shown to be a sensitive measure of epileptic seizure activity. While we could not automatically detect the full range of seizure behaviours, this method shows promise for future studies since X. laevis is a well-characterised and genetically tractable model organism.

Indexed as

LarvaPentylenetetrazoleSeizuresXenopus laevis4-AminopyridineAnimalsAnticonvulsantsBehavior, AnimalConvulsantsDisease Models, AnimalSwimmingValproic Acid4-AminopyridineAnticonvulsantsConvulsantsPentylenetetrazoleValproic AcidAfrican clawed frogEpilepsyseizure behaviourTopScanXenopus laevis

Identifiers

PMID37129175
PMCPMC11591405
OpenAlexW4367668982

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.