Evidence map›Paper›PMID 38893448›Full record

ArticleMolecules (Basel, Switzerland)2024

Assessment of the Novel Anti-Seizure Potential of Validamycin A Using Zebrafish Epilepsy Model.

Eunhye Lee, Amit Banik, Ki-Baek Lee, Seung Min Sim, Ah Hyun Kil, Byung Joon Hwang, Yun Kee

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Eunhye LeeDepartment of Biomedical Science, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
Amit BanikInterdisciplinary Graduate Program in Environmental and Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.ORCID 0009-0005-3795-9383
Ki-Baek LeeZefit Inc., Daegu 43017, Republic of Korea.
Seung Min SimDepartment of Biomedical Science, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
Ah Hyun KilDepartment of Molecular Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
Byung Joon HwangDepartment of Molecular Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
Yun KeeDepartment of Molecular Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.ORCID 0000-0003-2764-1468

Funding

Korea Disease Control and Prevention Agency 2020-ER6902-01Ministry of Education NRF-2020R1I1A3063583Ministry of Science and ICT NRF-2019M3C7A1031836
6 · The paper itself

Abstract

Epilepsy is a prevalent neurological disorder characterized by recurrent seizures. Validamycin A (VA) is an antibiotic fungicide that inhibits trehalase activity and is widely used for crop protection in agriculture. In this study, we identified a novel function of VA as a potential anti-seizure medication in a zebrafish epilepsy model. Electroencephalogram (EEG) analysis demonstrated that VA reduced pentylenetetrazol (PTZ)-induced seizures in the brains of larval and adult zebrafish. Moreover, VA reduced PTZ-induced irregular movement in a behavioral assessment of adult zebrafish. The developmental toxicity test showed no observable anatomical alteration when the zebrafish larvae were treated with VA up to 10 µM within the effective range. The median lethal dose of VA in adult zebrafish was > 14,000 mg/kg. These results imply that VA does not demonstrate observable toxicity in zebrafish at concentrations effective for generating anti-seizure activity in the EEG and alleviating abnormal behavior in the PTZ-induced epileptic model. Furthermore, the effectiveness of VA was comparable to that of valproic acid. These results indicate that VA may have a potentially safer anti-seizure profile than valproic acid, thus offering promising prospects for its application in agriculture and medicine.

Indexed as

AnticonvulsantsDisease Models, AnimalEpilepsyPentylenetetrazoleZebrafishAnimalsBrainElectroencephalographyInositolLarvaSeizuresValproic AcidAnticonvulsantsInositolPentylenetetrazolevalidamycin AValproic Acidangular velocityantibiotic fungicideanti-seizure activityelectroencephalogramvalidamycin Azebrafish epilepsy model

Identifiers

PMID38893448
PMCPMC11173475

What OpenQuestion holds

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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.