Evidence map›Paper›PMID 32456274›Full record

ReviewMolecules (Basel, Switzerland)2020

Anti-aggregation Effects of Phenolic Compounds on α-synuclein.

Kenjiro Ono, Mayumi Tsuji, Tritia R Yamasaki, Giulio M Pasinetti

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  9. Article
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  12. Phytochemical and Pharmacological Research inPlants (Basel, Switzerland) · 2022
    Article
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  14. Review
  15. Review
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

4 authors at 3 institutions in 2 countries.

Kenjiro OnoDivision of Neurology, Department of Internal Medicine, School of Medicine, Showa University, Tokyo 142-8666, Japan.ORCID 0000-0001-8454-6155
Mayumi TsujiPharmacological Research Center, Showa University, Tokyo 142-8666, Japan.
Tritia R YamasakiDepartment of Neurology, University of Kentucky, Lexington, KY 40536, USA.ORCID 0000-0002-4046-274X
Giulio M PasinettiDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York City, NY 10029, USA.ORCID 0000-0002-1524-5196
Showa University · JPIcahn School of Medicine at Mount Sinai · USUniversity of Kentucky · US

Funding

Institutional Career Development CoreKL2TR001996 · NCATS · UNIVERSITY OF KENTUCKY · PI BUSH, MATTHEW LEE, KELLY, THOMAS H. · 2016 to 2025
$7.1M
Testing Culturally Tailored Peer Groups for HIV Prevention for Couples in MalawiR01TW007965 · FIC · UNIVERSITY OF MALAWI · PI MBWEZA, ELLEN · 2007 to 2011
$253k
Grants-in-Aid for Scientific Research (Kakenhi) from the Japan Society for the Promotion of Science (JSPS) JP19K07965Grants-in-Aid for Scientific Research (Kakenhi) from the Japan Society for the Promotion of Science (JSPS) JP19K11698Japan Agency for Medical Research and Development 16dk0207021h0001NCATS NIH HHS KL2 TR001996NCCIH NIH HHS P50Office of Dietary Supplements AT008661-01
6 · The paper itself

Abstract

The aggregation and deposition of α-synuclein (αS) are major pathologic features of Parkinson's disease, dementia with Lewy bodies, and other α-synucleinopathies. The propagation of αS pathology in the brain plays a key role in the onset and progression of clinical phenotypes. Thus, there is increasing interest in developing strategies that attenuate αS aggregation and propagation. Based on cumulative evidence that αS oligomers are neurotoxic and critical species in the pathogenesis of α-synucleinopathies, we and other groups reported that phenolic compounds inhibit αS aggregation including oligomerization, thereby ameliorating αS oligomer-induced cellular and synaptic toxicities. Heterogeneity in gut microbiota may influence the efficacy of dietary polyphenol metabolism. Our recent studies on the brain-penetrating polyphenolic acids 3-hydroxybenzoic acid (3-HBA), 3,4-dihydroxybenzoic acid (3,4-diHBA), and 3-hydroxyphenylacetic acid (3-HPPA), which are derived from gut microbiota-based metabolism of dietary polyphenols, demonstrated an in vitro ability to inhibit αS oligomerization and mediate aggregated αS-induced neurotoxicity. Additionally, 3-HPPA, 3,4-diHBA, 3-HBA, and 4-hydroxybenzoic acid significantly attenuated intracellular αS seeding aggregation in a cell-based system. This review focuses on recent research developments regarding neuroprotective properties, especially anti-αS aggregation effects, of phenolic compounds and their metabolites by the gut microbiome, including our findings in the pathogenesis of α-synucleinopathies.

Indexed as

alpha-SynucleinBrainHumansLewy Body DiseaseParkinson DiseasePhenolsProtein Aggregation, PathologicalSynucleinopathiesalpha-SynucleinPhenolsgut microbiomeParkinson’s diseasephenolic compoundsα-synuclein

Identifiers

PMID32456274
PMCPMC7288075
OpenAlexW3027550282

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.