Evidence map›Paper›PMID 30469496›Full record

ArticleToxins2018

Parawixin2 Protects Hippocampal Cells in Experimental Temporal Lobe Epilepsy.

José Luiz Liberato, Lívea Dornela Godoy, Alexandra Olimpio Siqueira Cunha, Marcia Renata Mortari, Rene de Oliveira Beleboni, Andréia C K Fontana, Norberto Peporine Lopes, Wagner Ferreira Dos Santos

Open access · goldAbstract read
In one paragraph

Article in Toxins, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Neuroprotective properties of RT10, a fraction isolated fromThe journal of venomous animals and toxins including tropical diseases · 2019
    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

8 authors at 4 institutions in 2 countries.

José Luiz LiberatoNeurobiology and Venoms Laboratory (LNP), Department of Biology, College of Philosophy, Sciences and Literature of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14040-901 São Paulo, Brazil. jll@usp.br.ORCID 0000-0002-6538-8312
Lívea Dornela GodoyNeurobiology and Venoms Laboratory (LNP), Department of Biology, College of Philosophy, Sciences and Literature of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14040-901 São Paulo, Brazil. liveagodoy@usp.br.ORCID 0000-0003-4667-3553
Alexandra Olimpio Siqueira CunhaNeurobiology and Venoms Laboratory (LNP), Department of Biology, College of Philosophy, Sciences and Literature of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14040-901 São Paulo, Brazil. alecunha@usp.br.
Marcia Renata MortariLaboratory of Neuropharmacology, Department of Physiological Sciences, Institute of Biological Sciences, University of Brasília, DF 70910-900 Brasília, Brazil. mmortari@unb.br.
Rene de Oliveira BeleboniDepartment of Biotechnology/School of Medicine, University of Ribeirão Preto, Av. Costábile Romano, 2201, Ribeirão Preto, 14096-900 São Paulo, Brazil. rbeleboni@unaerp.br.
Andréia C K FontanaDepartment of Pharmacology and Physiology, Drexel University College of Medicine, 245 N. 15th Street, Philadelphia, PA 19102, USA. acm83@drexel.edu.ORCID 0000-0002-4791-8746
Norberto Peporine LopesNPPNS, Department of Physics and Chemistry, College of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, SP, Brazil, Av. do Cafe s/n, Ribeirão Preto, 14040-903 São Paulo, Brazil. npelopes@fcfrp.usp.br.ORCID 0000-0002-8159-3658
Wagner Ferreira Dos SantosNeurobiology and Venoms Laboratory (LNP), Department of Biology, College of Philosophy, Sciences and Literature of Ribeirão Preto, University of São Paulo, Av. Bandeirantes, 3900, Ribeirão Preto, 14040-901 São Paulo, Brazil. wagnerf@usp.br.
Universidade de São Paulo · BRDrexel University · USUniversidade de Brasília · BRUniversidade de Ribeirão Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is considered as one of the major disabling neuropathologies. Almost one third of adult patients with temporal lobe epilepsy (TLE) do not respond to current antiepileptic drugs (AEDs). Additionally, most AEDs do not have neuroprotective effects against the inherent neurodegenerative process underlying the hippocampal sclerosis on TLE. Dysfunctions in the GABAergic neurotransmission may contribute not only to the onset of epileptic activity but also constitute an important system for therapeutic approaches. Therefore, molecules that enhance GABA inhibitory effects could open novel avenues for the understanding of epileptic plasticity and for drug development. Parawixin2, a compound isolated from

Indexed as

AnimalsDisease Models, AnimalEpilepsy, Temporal LobeHippocampusMaleNeuronsNeuroprotective AgentsRats, WistarSpider VenomsUrea2-amino-5-ureidopentanamideNeuroprotective AgentsSpider VenomsUreaGABA uptake inhibitorhippocampal lost cellsneuroprotectionParawixia bistriataParawixin2pilocarpine modelspider toxintemporal lobe epilepsy

Identifiers

PMID30469496
PMCPMC6316435
OpenAlexW2900715364

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.