Evidence map›Paper›PMID 34578477›Full record

ArticleNanomaterials (Basel, Switzerland)2021

Tuning the Reduction of Graphene Oxide Nanoflakes Differently Affects Neuronal Networks in the Zebrafish.

Giuseppe Di Mauro, Rossana Rauti, Raffaele Casani, George Chimowa, Anne Marie Galibert, Emmanuel Flahaut, Giada Cellot, Laura Ballerini

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2021. 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
–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

7 citing papers in PubMed.

  1. Improving our understanding of the biology of aging: findings from the Age-It Research Program.The journals of gerontology. Series B, Psychological sciences and social sciences · 2025
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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.

Giuseppe Di MauroNeuron Physiology and Technology Lab, International School for Advanced Studies (SISSA), Neuroscience, Via Bonomea 265, 34136 Trieste, Italy.
Rossana RautiNeuron Physiology and Technology Lab, International School for Advanced Studies (SISSA), Neuroscience, Via Bonomea 265, 34136 Trieste, Italy.
Raffaele CasaniNeuron Physiology and Technology Lab, International School for Advanced Studies (SISSA), Neuroscience, Via Bonomea 265, 34136 Trieste, Italy.
George ChimowaCIRIMAT, UMR CNRS 5085, Université Toulouse Paul Sabatier, Bat. CIRIMAT, 118 Route de Narbonne, CEDEX 9, 31062 Toulouse, France.ORCID 0000-0002-7421-1068
Anne Marie GalibertCIRIMAT, UMR CNRS 5085, Université Toulouse Paul Sabatier, Bat. CIRIMAT, 118 Route de Narbonne, CEDEX 9, 31062 Toulouse, France.
Emmanuel FlahautCIRIMAT, UMR CNRS 5085, Université Toulouse Paul Sabatier, Bat. CIRIMAT, 118 Route de Narbonne, CEDEX 9, 31062 Toulouse, France.ORCID 0000-0001-8344-6902
Giada CellotNeuron Physiology and Technology Lab, International School for Advanced Studies (SISSA), Neuroscience, Via Bonomea 265, 34136 Trieste, Italy.ORCID 0000-0001-9198-8402
Laura BalleriniNeuron Physiology and Technology Lab, International School for Advanced Studies (SISSA), Neuroscience, Via Bonomea 265, 34136 Trieste, Italy.ORCID 0000-0001-8420-0787

Funding

Horizon 2020 881603
6 · The paper itself

Abstract

The increasing engineering of biomedical devices and the design of drug-delivery platforms enriched by graphene-based components demand careful investigations of the impact of graphene-related materials (GRMs) on the nervous system. In addition, the enhanced diffusion of GRM-based products and technologies that might favor the dispersion in the environment of GRMs nanoparticles urgently requires the potential neurotoxicity of these compounds to be addressed. One of the challenges in providing definite evidence supporting the harmful or safe use of GRMs is addressing the variety of this family of materials, with GRMs differing for size and chemistry. Such a diversity impairs reaching a unique and predictive picture of the effects of GRMs on the nervous system. Here, by exploiting the thermal reduction of graphene oxide nanoflakes (GO) to generate materials with different oxygen/carbon ratios, we used a high-throughput analysis of early-stage zebrafish locomotor behavior to investigate if modifications of a specific GRM chemical property influenced how these nanomaterials affect vertebrate sensory-motor neurophysiology-exposing zebrafish to GO downregulated their swimming performance. Conversely, reduced GO (rGO) treatments boosted locomotor activity. We concluded that the tuning of single GRM chemical properties is sufficient to produce differential effects on nervous system physiology, likely interfering with different signaling pathways.

Indexed as

graphene oxidereduced graphene oxidesensory-motor nervous systemsynapseszebrafish larvae

Identifiers

PMID34578477
PMCPMC8468975

What OpenQuestion holds

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LicenceCC BY
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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.