Evidence map›Paper›PMID 30594901›Full record

ArticleRedox biology2019

Old age-associated phenotypic screening for Alzheimer's disease drug candidates identifies sterubin as a potent neuroprotective compound from Yerba santa.

Wolfgang Fischer, Antonio Currais, Zhibin Liang, Antonio Pinto, Pamela Maher

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

47 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Chemical Composition ofMolecules (Basel, Switzerland) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Evidence of Oxytosis/Ferroptosis in Niemann-Pick Disease Type C.International journal of molecular sciences · 2025
    Article
  9. Article
  10. Review
  11. Neuroprotective and anti-inflammatory activity ofFrontiers in pharmacology · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. The role of ferroptosis in neurodegenerative diseases.Frontiers in cellular neuroscience · 2024
    Review
  19. Review
  20. Protective effect of sterubin against neurochemical and behavioral impairments in rotenone-induced Parkinson's disease.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    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

5 authors at 1 institution in 1 country.

Wolfgang FischerThe Salk Institute for Biological Studies, 10010 North Torrey Pines Rd., La Jolla, CA 92037, United States.
Antonio CurraisThe Salk Institute for Biological Studies, 10010 North Torrey Pines Rd., La Jolla, CA 92037, United States.
Zhibin LiangThe Salk Institute for Biological Studies, 10010 North Torrey Pines Rd., La Jolla, CA 92037, United States.
Antonio PintoThe Salk Institute for Biological Studies, 10010 North Torrey Pines Rd., La Jolla, CA 92037, United States.
Pamela MaherThe Salk Institute for Biological Studies, 10010 North Torrey Pines Rd., La Jolla, CA 92037, United States. Electronic address: pmaher@salk.edu.
Salk Institute for Biological Studies · US

Funding

The Contribution of Old Age-Associated Proteotoxicity to Inflammation and DementiaRF1AG054714 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI FISCHER, WOLFGANG H, MAHER, PAMELA ANNE · 2017 to 2017
$3.6M
Identification of Old-Age-Associated Alzheimer's Disease Drug TargetsR01AG046153 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI MAHER, PAMELA ANNE, SCHUBERT, DAVID R · 2014 to 2018
$2.9M
A Hybrid Quadrupole-Orbitrap LC/MSS10OD021815 · OD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SAGHATELIAN, ALAN · 2016 to 2016
$580k
NIA NIH HHS R01 AG046153NIA NIH HHS RF1 AG054714NIH HHS S10 OD021815
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most frequent age-associated dementia with no treatments that can prevent or slow its progression. Since age is by far the major risk factor for AD, there is a strong rationale for an alternative approach to drug discovery based upon the biology of aging. Phenotypic screening assays that reflect multiple, age-associated neurotoxicity pathways rather than single molecular targets can identify compounds that have therapeutic efficacy by targeting aspects of aging that contribute to AD pathology. And, while the suitability of any single assay can be questioned, a combination of assays can make reliable predictions about the neuroprotective effects of compounds in vivo. Therefore, our lab has developed a combination of phenotypic screening assays that are ideally suited not only to identify novel neuroprotective compounds for the treatment of AD but also their target pathways, thereby potentially providing new therapeutic targets for disease treatment. Using these assays, we screened a large library of extracts from plants with identified pharmacological uses. Analysis of one of these extracts from the plant Yerba santa (Eriodictyon californicum) identified the flavanone sterubin as the active component and further studies showed it to be a potent neuroprotective and anti-inflammatory compound.

Indexed as

PhenotypeAnimalsChromatography, High Pressure LiquidDrug Evaluation, PreclinicalEriodictyonHumansMass SpectrometryMiceNeuroprotectionNeuroprotective AgentsPC12 CellsPlant ExtractsRatsReactive Oxygen SpeciesReproducibility of ResultsNeuroprotective AgentsPlant ExtractsReactive Oxygen SpeciesATF4FerroptosisGlutathioneInflammationNrf2Oxidative stress

Identifiers

PMID30594901
PMCPMC6309122
OpenAlexW2905974310

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.