Evidence map›Paper›PMID 37990437›Full record

ArticleCNS neuroscience & therapeutics2024

Icaritin greatly attenuates β-amyloid-induced toxicity in vivo.

Liangxian Li, Zaiwa Wei, Yafang Tang, Mingyue Jin, Hua Yao, Xia Li, Qinghua Li, Jie Tan, Bo Xiao

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Gene model for the ortholog ofmicroPublication biology · 2026
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  6. Trehalose improves the movement ability of AβTranslational neuroscience · 2024
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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

9 authors at 1 institution in 1 country.

Liangxian LiLaboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin, China.
Zaiwa WeiGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Yafang TangClinical Research Center for Neurological Diseases of Guangxi Province, Affiliated Hospital of Guilin Medical University, Guilin, China.
Mingyue JinGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Hua YaoGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Xia LiGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Qinghua LiGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Jie TanGuangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical University, Guilin, China.
Bo XiaoLaboratory of Respiratory Disease, Affiliated Hospital of Guilin Medical University, Guilin, China.ORCID 0009-0003-3512-8645
Guilin Medical University · CN

Funding

Open Project Program of Guangxi Key Laboratory of Brain and Cognitive Neuroscience GKLBCN-20190103Open Project Program of Guangxi Key Laboratory of Brain and Cognitive Neuroscience GKLBCN-20190105-04Open Project Program of Guangxi Key Laboratory of Brain and Cognitive Neuroscience GKLBCN-202106-02Young and Middle aged Teachers' Basic Research Ability Improvement Project of Universities in Guangxi 2020KY12012Young and Middle aged Teachers' Basic Research Ability Improvement Project of Universities in Guangxi 2023KY0522Young and Middle aged Teachers' Basic Research Ability Improvement Project of Universities in Guangxi 2023KY0541
6 · The paper itself

Abstract

aimsThe accumulation and deposition of β-amyloid (Aβ) has always been considered a major pathological feature of Alzheimer's disease (AD). The latest and mainstream amyloid cascade hypothesis indicates that all the main pathological changes in AD are attributed to the accumulation of soluble Aβ. However, the exploration of therapeutic drugs for Aβ toxicity has progressed slowly. This study aims to investigate the protective effects of Icaritin on the Aβ-induced Drosophila AD model and its possible mechanism.

methodsTo identify the effects of Icaritin on AD, we constructed an excellent Drosophila AD model named Aβ

resultsWe discovered that Icaritin almost completely rescues the climbing ability, flight ability, and longevity of Aβ

conclusionThis study suggested that Icaritin is a potential drug to deal with the toxicity of Aβ

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesFlavonoidsAnimalsDrosophilaHumansOxidative StressAmyloid beta-PeptidesFlavonoidsicaritinAlzheimer's diseaseenergy metabolismIcaritinmitochondriaoxidative stress

Identifiers

PMID37990437
PMCPMC11017459
OpenAlexW4388921952

What OpenQuestion 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 OpenQuestion graph.