Evidence map›Paper›PMID 29555973›Full record

ArticleScientific reports2018

Analysis of the neurotoxic effects of neuropathic organophosphorus compounds in adult zebrafish.

Melissa Faria, Inmaculada Fuertes, Eva Prats, Jose Luis Abad, Francesc Padrós, Cristian Gomez-Canela, Josefina Casas, Jorge Estevez, Eugenio Vilanova, Benjamin Piña and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Ophthalmic genetics · 2023
    Review
  5. Article
  6. Article
  7. 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

11 authors at 5 institutions in 1 country.

Melissa FariaDepartment of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Inmaculada FuertesDepartment of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Eva PratsCID-CSIC, Jordi Girona 18, E-08034, Barcelona, Spain.ORCID 0000-0001-7838-2027
Jose Luis AbadDepartment of Biomedicinal Chemistry, Institute for Advanced Chemistry of Catalonia, (IQAC-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Francesc PadrósFish Diseases Diagnostic Service, Facultat de Veterinaria Universitat Autònoma de Barcelona, 08190, Bellaterra (Cerdanyola del Vallès), Spain.
Cristian Gomez-CanelaDepartment of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Josefina CasasDepartment of Biomedicinal Chemistry, Institute for Advanced Chemistry of Catalonia, (IQAC-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Jorge EstevezInstitute of Bioengineering, University "Miguel Hernandez" of Elche, Alicante, Spain.
Eugenio VilanovaInstitute of Bioengineering, University "Miguel Hernandez" of Elche, Alicante, Spain.
Benjamin PiñaDepartment of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain.
Demetrio RaldúaDepartment of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18, E-08034, Barcelona, Spain. drpqam@cid.csic.es.ORCID 0000-0001-5256-1641
Institute of Environmental Assessment and Water Research · ESInstitute of Advanced Chemistry of Catalonia · ESUniversitat de Miguel Hernández d'Elx · ESCentro de Investigación y Desarrollo · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibition and aging of neuropathy target esterase (NTE) by exposure to neuropathic organophosphorus compounds (OPs) can result in OP-induced delayed neuropathy (OPIDN). In the present study we aimed to build a model of OPIDN in adult zebrafish. First, inhibition and aging of zebrafish NTE activity were characterized in the brain by using the prototypic neuropathic compounds cresyl saligenin phosphate (CBDP) and diisopropylphosphorofluoridate (DFP). Our results show that, as in other animal models, zebrafish NTE is inhibited and aged by both neuropathic OPs. Then, a neuropathic concentration inhibiting NTE activity by at least 70% for at least 24 h was selected for each compound to analyze changes in phosphatidylcholines (PCs), lysophosphatidylcholines (LPCs) and glycerolphosphocholine (GPC) profiles. In spite to the strong inhibition of the NTE activity found for both compounds, only a mild increase in the LPCs level was found after 48 h of the exposure to DFP, and no effect were observed by CBDP. Moreover, histopathological evaluation and motor function outcome analyses failed to find any neurological abnormalities in the exposed fish. Thus, our results strongly suggest that zebrafish is not a suitable species for the development of an experimental model of human OPIDN.

Indexed as

ZebrafishAnimalsBrainCarboxylic Ester HydrolasesDose-Response Relationship, DrugLipid MetabolismLocomotionNeurotoxinsOrganophosphorus CompoundsPeripheral Nervous System DiseasesCarboxylic Ester Hydrolasesneurotoxic esteraseNeurotoxinsOrganophosphorus Compounds

Identifiers

PMID29555973
PMCPMC5859099
OpenAlexW2803122871

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.