Evidence map›Paper›PMID 37507902›Full record

ArticleAntioxidants (Basel, Switzerland)2023

Inhibition of Acetylcholinesterase and Amyloid-β Aggregation by Piceatannol and Analogs: Assessing In Vitro and In Vivo Impact on a Murine Model of Scopolamine-Induced Memory Impairment.

Yi-Yan Sie, Liang-Chieh Chen, Cai-Jhen Li, Yu-Hsiang Yuan, Sheng-Hung Hsiao, Mei-Hsien Lee, Ching-Chiung Wang, Wen-Chi Hou

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

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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 at 3 institutions in 2 countries.

Yi-Yan SiePh.D. Program in Clinical Drug Development of Herbal Medicine, College of Pharmacy, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0002-2692-0556
Liang-Chieh ChenDepartment of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90089, USA.ORCID 0000-0003-4891-3848
Cai-Jhen LiGraduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.
Yu-Hsiang YuanGraduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.
Sheng-Hung HsiaoGraduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.
Mei-Hsien LeeGraduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0001-8592-9326
Ching-Chiung WangSchool of Pharmacy, Taipei Medical University, Taipei 110, Taiwan.
Wen-Chi HouGraduate Institute of Pharmacognosy, Taipei Medical University, Taipei 110, Taiwan.ORCID 0000-0002-9565-7018
Taipei Medical University · TWTaipei Medical University Hospital · TWUniversity of Southern California · US

Funding

Council of Agriculture, Executive Yuan, ROC 111AS-14.1.1-ST-a2
6 · The paper itself

Abstract

Currently, no drug is effective in delaying the cognitive impairment of Alzheimer's disease, which ranks as one of the top 10 causes of death worldwide. Hydroxylated stilbenes are active compounds that exist in fruit and herbal plants. Piceatannol (PIC) and gnetol (GNT), which have one extra hydroxyl group in comparison to resveratrol (RSV), and rhapontigenin (RHA) and isorhapontigenin (isoRHA), which were metabolized from PIC in vivo and contain the same number of hydroxyl groups as RSV, were evaluated for their effects on Alzheimer's disease-associated factors in vitro and in animal experiments. Among the five hydroxylated stilbenes, PIC was shown to be the most active in DPPH radical scavenging and in inhibitory activities against acetylcholinesterase and amyloid-β peptide aggregations, with concentrations for half-maximal inhibitions of 40.2, 271.74, and 0.48 μM. The different interactions of the five hydroxylated stilbenes with acetylcholinesterase or amyloid-β were obtained by molecular docking. The scopolamine-induced ICR mice fed with PIC (50 mg/kg) showed an improved learning behavior in the passive avoidance tests and had significant differences (

Indexed as

acetylcholinesteraseamyloid-β peptidehydroxylated stilbenesneurite outgrowthpassive avoidance testpiceatannol (PIC)scopolamine

Identifiers

PMID37507902
PMCPMC10376691
OpenAlexW4382792068

What Socratic holds

Textmetadata
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 Socratic graph.