Evidence map›Paper›PMID 28575152›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2018

Fisetin Reduces the Impact of Aging on Behavior and Physiology in the Rapidly Aging SAMP8 Mouse.

Antonio Currais, Catherine Farrokhi, Richard Dargusch, Aaron Armando, Oswald Quehenberger, David Schubert, Pamela Maher

Open access · bronzeAbstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.2field-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

66 citing papers in PubMed, 131 citations in OpenAlex.

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  3. Fisetin Mitigates Ferroptosis and Promotes Remyelination in a Cuprizone Model of Multiple Sclerosis.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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  15. A plant flavonol and genetic suppressors rescue a pathogenic mutation associated with kinesin in neurons.Proceedings of the National Academy of Sciences of the United States of America · 2024
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6 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Antonio CurraisDepartment of Cellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, California.
Catherine FarrokhiDepartment of Cellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, California.
Richard DarguschDepartment of Cellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, California.
Aaron ArmandoDepartment of Medicine, University of California San Diego, La Jolla.
Oswald QuehenbergerDepartment of Medicine, University of California San Diego, La Jolla.
David SchubertDepartment of Cellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, California.
Pamela MaherDepartment of Cellular Neurobiology, The Salk Institute for Biological Studies, La Jolla, California.
Salk Institute for Biological Studies · USUniversity of California, San Diego · US

Funding

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
Pan-Lipoxygenase Inhibitors for CNS DiseaseR01AG035055 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SCHUBERT, DAVID R · 2010 to 2014
$1.9M
Modulation of the Innate Immune Response by Fisetin Derivatives for the Treatment of ADR42AI104034 · NIAID · VIROGENICS, INC. · PI MAHER, PAMELA ANNE · 2016 to 2017
$1.5M
NIAID NIH HHS R42 AI104034NIA NIH HHS R01 AG035055NIA NIH HHS R01 AG046153
6 · The paper itself

Abstract

Alzheimer's disease (AD) is rarely addressed in the context of aging even though there is an overlap in pathology. We previously used a phenotypic screening platform based on old age-associated brain toxicities to identify the flavonol fisetin as a potential therapeutic for AD and other age-related neurodegenerative diseases. Based on earlier results with fisetin in transgenic AD mice, we hypothesized that fisetin would be effective against brain aging and cognitive dysfunction in rapidly aging senescence-accelerated prone 8 (SAMP8) mice, a model for sporadic AD and dementia. An integrative approach was used to correlate protein expression and metabolite levels in the brain with cognition. It was found that fisetin reduced cognitive deficits in old SAMP8 mice while restoring multiple markers associated with impaired synaptic function, stress, and inflammation. These results provide further evidence for the potential benefits of fisetin for the treatment of age-related neurodegenerative diseases.

Indexed as

AgingAlzheimer DiseaseAnimalsBehavior, AnimalBlotting, WesternDisease Models, AnimalEicosanoidsFlavonoidsFlavonolsImmunohistochemistryMaze LearningMetabolomicsMiceMice, TransgenicVisual PerceptionEicosanoidsfisetinFlavonoidsFlavonols

Identifiers

PMID28575152
PMCPMC5861950
OpenAlexW2621143613

What OpenQuestion holds

Textmetadata
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.