Evidence map›Paper›PMID 32997672›Full record

ArticlePloS one2020

Allium roseum L. extract inhibits amyloid beta aggregation and toxicity involved in Alzheimer's disease.

Abdelbasset Boubakri, Manuela Leri, Monica Bucciantini, Hanen Najjaa, Abdelkarim Ben Arfa, Massimo Stefani, Mohamed Neffati

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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  13. Effects of the Bark Resin Extract ofMolecules (Basel, Switzerland) · 2022
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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

7 authors.

Abdelbasset BoubakriLaboratoire des Ecosystèmes Pastoraux et Valorisation des Plantes Spontanées et des Micro-organismes Associés, Institut des Régions Arides, Médenine, Tunisia.ORCID 0000-0001-8755-8362
Manuela LeriDepartment of Clinical and Experimental Biomedical Sciences "Mario Serio", University of Florence, Viale Morgagni, Florence, Italy.
Monica BucciantiniDepartment of Clinical and Experimental Biomedical Sciences "Mario Serio", University of Florence, Viale Morgagni, Florence, Italy.
Hanen NajjaaLaboratoire des Ecosystèmes Pastoraux et Valorisation des Plantes Spontanées et des Micro-organismes Associés, Institut des Régions Arides, Médenine, Tunisia.
Abdelkarim Ben ArfaLaboratoire des Ecosystèmes Pastoraux et Valorisation des Plantes Spontanées et des Micro-organismes Associés, Institut des Régions Arides, Médenine, Tunisia.
Massimo StefaniDepartment of Clinical and Experimental Biomedical Sciences "Mario Serio", University of Florence, Viale Morgagni, Florence, Italy.
Mohamed NeffatiLaboratoire des Ecosystèmes Pastoraux et Valorisation des Plantes Spontanées et des Micro-organismes Associés, Institut des Régions Arides, Médenine, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allium roseum is an important medicinal and aromatic plant, specific to the North African flora and a rich source of important nutrients and bioactive molecules including flavonoids and organosulfur compounds whose biological activities and pharmacological properties are well known. In the present study, the inhibition of amyloid beta protein toxicity by the ethanolic extract of this plant is investigated for the first time. Preliminary biochemical analyses identified kæmpferol and luteolin-7-o-glucoside as the more abundant phenolic compounds. The effects of A. roseum extract (ARE) on aggregation and aggregate cytotoxicity of amyloid beta-42 (Aβ42), whose brain aggregates are a hallmark of Alzheimer's disease, were investigated by biophysical (ThT assay, Dynamic light scattering and transmission electron microscopy) and cellular assays (cytotoxicity, aggregate immunolocalization, ROS measurement and intracellular Ca2+ imaging). The biophysical data suggest that ARE affects the structure of the Aβ42 peptide, inhibits its polymerization, and interferes with the path of fibrillogenesis. The data with cultured cells shows that ARE reduces Aß42 aggregate toxicity by inhibiting aggregate binding to the cell membrane and by decreasing both oxidative stress and intracellular Ca2+. Accordingly, ARE could act as a neuroprotective factor against Aβ aggregate toxicity in Alzheimer's disease.

Indexed as

AlliumAlzheimer DiseaseAmyloid beta-PeptidesCalciumCell Line, TumorCell MembraneCytosolDrug Evaluation, PreclinicalDynamic Light ScatteringEthanolHumansMicroscopy, Electron, TransmissionNeuroprotective AgentsOxidative StressPeptide FragmentsPlant ExtractsAmyloid beta-Peptidesamyloid beta-protein (1-42)CalciumEthanolNeuroprotective AgentsPeptide FragmentsPlant ExtractsReactive Oxygen Species

Identifiers

PMID32997672
PMCPMC7526880

What OpenQuestion holds

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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.