Evidence map›Paper›PMID 28282918›Full record

ArticleInternational journal of molecular sciences2017

Zebrafish Embryo as an In Vivo Model for Behavioral and Pharmacological Characterization of Methylxanthine Drugs.

Ram Manohar Basnet, Michela Guarienti, Maurizio Memo

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. International journal of molecular sciences · 2024
    Article
  7. Article
  8. Article
  9. Bi-Allelic Mutations in ZebrafishInternational journal of molecular sciences · 2022
    Article
  10. Article
  11. Article
  12. Caffeine Inhibits Direct and Indirect Angiogenesis in Zebrafish Embryos.International journal of molecular sciences · 2021
    Article
  13. Article
  14. Cells · 2020
    Article
  15. The Downregulation ofFrontiers in cell and developmental biology · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Zebrafish as a Model to Evaluate Nanoparticle Toxicity.Nanomaterials (Basel, Switzerland) · 2018
    Review
  20. 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

3 authors at 1 institution in 1 country.

Ram Manohar BasnetDepartment of Molecular and Translational Medicine, University of Brescia, Viale Europa, 11, 25123 Brescia, Italy. r.basnet@unibs.it.
Michela GuarientiDepartment of Molecular and Translational Medicine, University of Brescia, Viale Europa, 11, 25123 Brescia, Italy. michela.guarienti@unibs.it.
Maurizio MemoDepartment of Molecular and Translational Medicine, University of Brescia, Viale Europa, 11, 25123 Brescia, Italy. maurizio.memo@unibs.it.
University of Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Zebrafish embryo is emerging as an important tool for behavior analysis as well as toxicity testing. In this study, we compared the effect of nine different methylxanthine drugs using zebrafish embryo as a model. We performed behavioral analysis, biochemical assay and Fish Embryo Toxicity (FET) test in zebrafish embryos after treatment with methylxanthines. Each drug appeared to behave in different ways and showed a distinct pattern of results. Embryos treated with seven out of nine methylxanthines exhibited epileptic-like pattern of movements, the severity of which varied with drugs and doses used. Cyclic AMP measurement showed that, despite of a significant increase in cAMP with some compounds, it was unrelated to the observed movement behavior changes. FET test showed a different pattern of toxicity with different methylxanthines. Each drug could be distinguished from the other based on its effect on mortality, morphological defects and teratogenic effects. In addition, there was a strong positive correlation between the toxic doses (TC

Indexed as

AnimalsCyclic AMPEmbryo, NonmammalianLocomotionTeratogensToxicity TestsXanthinesZebrafishCyclic AMPmethylxanthineTeratogensXanthinesbehaviorcyclic AMPFish Embryo Toxicity testmethylxanthinemovementzebrafish embryos

Identifiers

PMID28282918
PMCPMC5372612
OpenAlexW2594287301

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.