Evidence map›Paper›PMID 30303965›Full record

ArticlePloS one2018

Atomic force microscopy reveals new biophysical markers for monitoring subcellular changes in oxidative injury: Neuroprotective effects of quercetin at the nanoscale.

Maja Jazvinšćak Jembrek, Josipa Vlainić, Vida Čadež, Suzana Šegota

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 20 citations in OpenAlex.

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  16. Neuroprotective Potential of Secondary Metabolites fromMolecules (Basel, Switzerland) · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Maja Jazvinšćak JembrekDivision of Molecular Medicine, Ruđer Bošković Institute, Zagreb, Croatia.
Josipa VlainićDivision of Molecular Medicine, Ruđer Bošković Institute, Zagreb, Croatia.
Vida ČadežDivision of Physical Chemistry, Ruđer Bošković Institute, Zagreb, Croatia.
Suzana ŠegotaDivision of Physical Chemistry, Ruđer Bošković Institute, Zagreb, Croatia.ORCID 0000-0001-6416-3835
Ruđer Bošković Institute · HRCatholic University of Croatia · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress has been recognised as an important pathological mechanism underlying the development of neurodegenerative diseases. The biomarkers for assessing the degree of oxidative stress have been attracting much interest because of their potential clinical relevance in understanding the cellular effects of free radicals and evaluation of the efficacy of drug treatment. Here, an interdisciplinary approach using atomic force microscopy (AFM) and cellular and biological molecular methods were used to investigate oxidative damage in P19 neurons and to reveal the underlying mechanism of protective action of quercetin. Biological methods demonstrated the oxidative damage of P19 neurons and showed that quercetin improved neuronal survival by preventing H2O2-induced p53 and Bcl-2 down-regulation and modulated Akt and ERK1/2 signalling pathways. For the first time, AFM was employed to evaluate morphologically (roughness, height, Feret dimension) and nanomechanical (elasticity) properties in H2O2-induced neuronal damage. The AFM analysis revealed that quercetin suppressed H2O2-provoked changes in cell membrane elasticity and morphological properties, thus confirming its neuroprotective activity. The obtained results indicate the potential of AFM-measured parameters as a biophysical markers of oxidative stress-induced neurodegeneration. In general, our study suggests that AFM can be used as a highly valuable tool in other biomedical applications aimed at screening and monitoring of drug-induced effects at cellular level.

Indexed as

Microscopy, Atomic ForceOxidative StressAnimalsAntioxidantsBiomarkersCell Line, TumorElasticityGlutathioneHydrogen PeroxideMembrane Potential, MitochondrialMiceNanomedicineNeuronsNeuroprotective AgentsPolymerase Chain ReactionProto-Oncogene Proteins c-bcl-2AntioxidantsBiomarkersGlutathioneHydrogen PeroxideNeuroprotective AgentsProto-Oncogene Proteins c-bcl-2QuercetinReactive Oxygen SpeciesTumor Suppressor Protein p53

Identifiers

PMID30303965
PMCPMC6179194
OpenAlexW2809522062

What OpenQuestion holds

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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.