Evidence map›Paper›PMID 28441758›Full record

ArticleInternational journal of molecular sciences2017

Acteoside and Isoacteoside Protect Amyloid β Peptide Induced Cytotoxicity, Cognitive Deficit and Neurochemical Disturbances In Vitro and In Vivo.

Young-Ji Shiao, Muh-Hwan Su, Hang-Ching Lin, Chi-Rei Wu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Potential ofFood science & nutrition · 2026
    Article
  3. Review
  4. Acteoside exerts neuroprotective effects by preventing α-synuclein aggregation and oxidative stress in models of Parkinson's disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. The pharmacokinetic property and pharmacological activity of acteoside: A review.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Review
  16. Article
  17. Article
  18. Review
  19. Neuroprotective Potential of Verbascoside Isolated fromAntioxidants (Basel, Switzerland) · 2020
    Article
  20. 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 1 country.

Young-Ji ShiaoNational Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei 11490, Taiwan. yshiao@nricm.edu.tw.
Muh-Hwan SuSchool of Pharmacy, National Defense Medical Center, Taipei 11490, Taiwan. smh1027@syncorebio.com.
Hang-Ching LinSchool of Pharmacy, National Defense Medical Center, Taipei 11490, Taiwan. lhc@sinphar.com.tw.
Chi-Rei WuDepartment of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, College of Pharmacy, China Medical University, Taichung 40402, Taiwan. crw@mail.cmu.edu.tw.
National Defense Medical Center · TWChina Medical University · TWNational Research Institute of Chinese Medicine · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acteoside and isoacteoside, two phenylethanoid glycosides, coexist in some plants. This study investigates the memory-improving and cytoprotective effects of acteoside and isoacteoside in amyloid β peptide 1-42 (Aβ 1-42)-infused rats and Aβ 1-42-treated SH-SY5Y cells. It further elucidates the role of amyloid cascade and central neuronal function in these effects. Acteoside and isoacteoside ameliorated cognitive deficits, decreased amyloid deposition, and reversed central cholinergic dysfunction that were caused by Aβ 1-42 in rats. Acteoside and isoacteoside further decreased extracellular Aβ 1-40 production and restored the cell viability that was decreased by Aβ 1-42 in SH-SY5Y cells. Acteoside and isoacteoside also promoted Aβ 1-40 degradation and inhibited Aβ 1-42 oligomerization in vitro. However, the memory-improving and cytoprotective effects of isoacteoside exceeded those of acteoside. Isoacteoside promoted exploratory behavior and restored cortical and hippocampal dopamine levels, but acteoside did not. We suggest that acteoside and isoacteoside ameliorated the cognitive dysfunction that was caused by Aβ 1-42 by blocking amyloid deposition via preventing amyloid oligomerization, and reversing central neuronal function via counteracting amyloid cytotoxicity.

Indexed as

AcetylcholinesteraseAmyloid beta-PeptidesAnimalsBehavior, AnimalCell Line, TumorCell SurvivalCholineDopamineGlucosidesHippocampusHumansMaleMonoamine OxidaseNeuronsNorepinephrinePeptide FragmentsAcetylcholinesteraseacteosideAmyloid beta-Peptidesamyloid beta-protein (1-40)amyloid beta-protein (1-42)CholineDopamineGlucosidesisoacteosideMonoamine OxidaseNorepinephrinePeptide FragmentsPhenolsPolyphenolsProtective Agentsacetylcholineacteosideamyloid cascadeamyloid β peptideisoacetosideMorris water maze

Identifiers

PMID28441758
PMCPMC5412474
OpenAlexW2608430149

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.