Evidence map›Paper›PMID 38053575›Full record

ArticleThe journal of venomous animals and toxins including tropical diseases2023

Amanda Gomes da Silva, Mariana da Mata Alves, Admilson Aparecido da Cunha, Giovanna Arruda Caires, Irina Kerkis, Hugo Vigerelli, Juliana Mozer Sciani

Abstract read
In one paragraph

Article in The journal of venomous animals and toxins including tropical diseases, 2023. 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. Dihydropashanone Isolated fromInternational journal of molecular sciences · 2024
    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.

Amanda Gomes da SilvaIntegrated Pharmacology and Gastroenterology Unit (UNIFAG), Bragança Paulista, SP, Brazil.
Mariana da Mata AlvesLaboratory of Genetics, Butantan Institute, São Paulo, SP, Brazil.
Admilson Aparecido da CunhaLaboratory of Biochemistry and Biophysics, Butantan Institute, São Paulo, SP, Brazil.
Giovanna Arruda CairesLaboratory of Genetics, Butantan Institute, São Paulo, SP, Brazil.
Irina KerkisLaboratory of Genetics, Butantan Institute, São Paulo, SP, Brazil.
Hugo VigerelliLaboratory of Genetics, Butantan Institute, São Paulo, SP, Brazil.
Juliana Mozer ScianiLaboratory of Natural Products, Postgraduate Program in Health Sciences, São Francisco University, Bragança Paulista, SP, Brazil.ORCID 0000-0001-7213-206X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: In this study, we incubated Results: ELCF and certain fractions could prevent and treat the reduction of cell viability caused by Aβ42o in SH-SY5Y neuron-like cells. We found that one fraction (El50) reduced the oligomerized Aβ42 and the oxidative stress caused by the amyloid peptide through its antioxidant molecules, which in turn reduced cell death. Mass spectrometry analysis revealed that El50 comprises small molecules containing flavonoid antioxidants, such as phenylpyridazine and dihydroquercetin, and two peptides. Conclusion: Our results suggest that sea urchin molecules may interact with Aβ42o and oxidative stress, preventing or treating neurotoxicity, which may be useful in treating dementia.

Indexed as

Alzheimer’s diseaseamyloid peptide 42oxidative stressprotein clearancesea urchin

Identifiers

PMID38053575
PMCPMC10694836

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.