Evidence map›Paper›PMID 30935135›Full record

ArticleNutrients2019

Polyphenols Modulate Alzheimer's Amyloid Beta Aggregation in a Structure-Dependent Manner.

Huong T T Phan, Kaouthar Samarat, Yuzuru Takamura, Auriane F Azo-Oussou, Yasutaka Nakazono, Mun'delanji C Vestergaard

Abstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Review
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  18. assessment of antioxidant, neuroprotective, anti-urease and anti-tyrosinase capacities of leaves extracts.Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan · 2023
    Article
  19. The journal of venomous animals and toxins including tropical diseases · 2023
    Article
  20. Journal of traditional and complementary medicine · 2023
    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

6 authors.

Huong T T PhanJapan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi City, Ishikawa 923-1292, Japan. huongptt@hnue.edu.vn.
Kaouthar SamaratJapan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi City, Ishikawa 923-1292, Japan. k.samarat@gmail.com.
Yuzuru TakamuraJapan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi City, Ishikawa 923-1292, Japan. takamura@jaist.ac.jp.
Auriane F Azo-OussouDepartment of Food Science and Biotechnology, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-8580, Japan. oauriane1@gmail.com.
Yasutaka NakazonoDepartment of Food Science and Biotechnology, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-8580, Japan. yasutaka33ym@gmail.com.
Mun'delanji C VestergaardDepartment of Food Science and Biotechnology, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-8580, Japan. munde@agri.kagoshima-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some polyphenols, which are common natural compounds in fruits, vegetables, seeds, and oils, have been considered as potent inhibitors of amyloid beta (Aβ) aggregation, one critical pathogenic event in Alzheimer's disease (AD). However, the mechanisms by which polyphenols affect aggregation are not fully understood. In this study, we aimed to investigate the effect of two classes of polyphenols (flavonoids and stilbenes) on the self-assembly of Aβ_42, in particular, how this relates to structure. We found that the flavonoids gallocatechin gallate (GCG) and theaflavin (TF) could completely inhibit Aβ aggregation, while two stilbenes, resveratrol and its glucoside derivative piceid, could also suppress Aβ aggregation, but to a much lesser extent. Intriguingly, resveratrol accelerated the formation of Aβ fibrils before its decreasing effect on fibrillation was detected. Atomic force microscopy (AFM) images showed a huge mass of long and thin Aβ fibrils formed in the presence of resveratrol. Although the morphology was the same in the presence of piceid, the fibrils were sparse in the presence of picead. In the presence of flavonoids, Aβ morphology was unchanged from prior to incubation (0 h), in agreement with amyloid beta kinetics analysis using thioflavin-T fluorescence assay. The electrochemical data showed a higher ability of GCG and TF to interact with Aβ than resveratrol and piceid, which could be attributed to the presence of more aromatic rings and hydroxyl groups. In addition, the two flavonoids exhibited a similar propensity for Aβ aggregation, despite having some differences in their structure. However, in the case of stilbenes, the addition of a glucoside at C-7 slightly decreased anti-Aβ aggregation property compared to resveratrol. These findings contribute to a better understanding of the essential structural features of polyphenols required for inhibiting Aβ aggregation, and the possible mechanisms for modulating aggregation.

Indexed as

Protein AggregatesAmyloidAmyloid beta-PeptidesAntioxidantsMicroscopy, Atomic ForcePolyphenolsProtein ConformationAmyloidAmyloid beta-PeptidesAntioxidantsPolyphenolsProtein Aggregatesamyloid beta aggregationbioactivityflavonoidsmodulationpolyphenolstrans-stilbenes

Identifiers

PMID30935135
PMCPMC6521010

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Registered trials

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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.