Evidence map›Paper›PMID 39537765›Full record

ArticleScientific reports2024

Unraveling neuroprotection with Kv1.3 potassium channel blockade by a scorpion venom peptide.

Emidio Beraldo-Neto, Vanessa Florentino Ferreira, Hugo Vigerelli, Karolina Rosa Fernandes, Maria Aparecida Juliano, Ana Leonor Abrahao Nencioni, Daniel Carvalho Pimenta

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Peptide Fraction fromAntioxidants (Basel, Switzerland) · 2025
    Article
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.

Emidio Beraldo-NetoBiochemistry Laboratory, Butantan Institute, São Paulo, Brazil. emidio.beraldo@butantan.gov.br.ORCID 0000-0002-4735-5162
Vanessa Florentino FerreiraPharmacology Laboratory, Butantan Institute, São Paulo, Brazil.ORCID 0009-0002-0326-1647
Hugo VigerelliGenetics Laboratory, Butantan Institute, São Paulo, Brazil.ORCID 0000-0002-8197-2260
Karolina Rosa FernandesDepartment of Biophysics, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.ORCID 0000-0003-0462-5254
Maria Aparecida JulianoDepartment of Biophysics, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.ORCID 0000-0003-2994-0947
Ana Leonor Abrahao NencioniPharmacology Laboratory, Butantan Institute, São Paulo, Brazil.ORCID 0000-0002-1162-4201
Daniel Carvalho PimentaBiochemistry Laboratory, Butantan Institute, São Paulo, Brazil. dcpimenta@butantan.gov.br.ORCID 0000-0003-2406-0860

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 305525/2023-9Conselho Nacional de Desenvolvimento Científico e Tecnológico PIBICFinanciadora de Estudos e Projetos 01.09.0278.04Financiadora de Estudos e Projetos 01.12.0450.03Fundação de Amparo à Pesquisa do Estado de São Paulo 2018-13588-0Fundação de Amparo à Pesquisa do Estado de São Paulo 22/10148-4
6 · The paper itself

Abstract

Voltage-gated potassium channels play a crucial role in cellular repolarization and are potential therapeutic targets in neuroinflammatory disorders and neurodegenerative diseases. This study explores Tityus bahiensis scorpion venom for neuroactive peptides. We identified the αKtx12 peptide as a potent neuroprotective agent. In SH-SY5Y cells, αKtx12 significantly enhances viability, validating its pharmacological potential. And in the animal model, we elucidate central nervous system (CNS) mechanism of αKtx12 through neuroproteomic analyses highlighting αKtx12 as a valuable tool for characterizing neuroplasticity and neurotropism, revealing its ability to elicit more physiological responses. The peptide's potential to promote cell proliferation and neuroprotection suggests a role in functional recovery from nervous system injury or disease. This research unveils the neuroactive potential of scorpion venom-derived αKtx12's, offering insights into its pharmacological utility. The peptide's impact on neuronal processes suggests a promising avenue for therapeutic development, particularly in neurodegenerative conditions.

Indexed as

Kv1.3 Potassium ChannelNeuroprotective AgentsScorpion VenomsAnimalsCell Line, TumorCell ProliferationCell SurvivalHumansMiceNeuronsNeuroprotectionPeptidesPotassium Channel BlockersRatsKv1.3 Potassium ChannelNeuroprotective AgentsPeptidesPotassium Channel BlockersScorpion VenomsHippocampusKv1.3NeurotoxinPeptideScorpion toxinVoltage-gated potassium channelαKtx12

Identifiers

PMID39537765
PMCPMC11561340

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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.