Evidence map›Paper›PMID 37248899›Full record

ArticleJournal of Alzheimer's disease : JAD2023

Prodromal Glutamatergic Modulation with Riluzole Impacts Glucose Homeostasis and Spatial Cognition in Alzheimer's Disease Mice.

Caleigh A Findley, Samuel A McFadden, MaKayla F Cox, Lindsey N Sime, Mackenzie R Peck, Kathleen Quinn, Andrzej Bartke, Kevin N Hascup, Erin R Hascup

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2023. 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
1.2field-weighted citation impact, top 24% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Lifespan of male and female APP/PS1 and APPJournal of Alzheimer's disease : JAD · 2025
    Article
  5. Article
  6. Lifespan of male and female APP/PS1 and APPbioRxiv : the preprint server for biology · 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

9 authors at 1 institution in 1 country.

Caleigh A FindleyNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Samuel A McFaddenNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
MaKayla F CoxNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Lindsey N SimeNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Mackenzie R PeckNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Kathleen QuinnNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Andrzej BartkeDepartment of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Kevin N HascupNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Erin R HascupNeuroscience Institute, Dale and Deborah Smith Center for Alzheimer's Research and Treatment, Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.
Southern Illinois University School of Medicine · US

Funding

Sequelae of SARS-CoV-2 Infection in Alzheimer's DiseaseR01AG061937 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI HASCUP, ERIN R · 2018 to 2022
$4.0M
Glutamate neurotransmission in Alzheimer's disease progressionR01AG057767 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI HASCUP, ERIN R · 2018 to 2022
$3.2M
Developmental Programming of Mammalian AgingR21AG062985 · NIA · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI BARTKE, ANDRZEJ · 2020 to 2021
$418k
NIA NIH HHS R01 AG057767NIA NIH HHS R01 AG061937NIA NIH HHS R21 AG062985
6 · The paper itself

Abstract

backgroundPrior research supports a strong link between Alzheimer's disease (AD) and metabolic dysfunction that involves a multi-directional interaction between glucose, glutamatergic homeostasis, and amyloid pathology. Elevated soluble amyloid-β (Aβ) is an early biomarker for AD-associated cognitive decline that contributes to concurrent glutamatergic and metabolic dyshomeostasis in humans and male transgenic AD mice. Yet, it remains unclear how primary time-sensitive targeting of hippocampal glutamatergic activity may impact glucose regulation in an amyloidogenic mouse model. Previous studies have illustrated increased glucose uptake and metabolism using a neuroprotective glutamate modulator (riluzole), supporting the link between glucose and glutamatergic homeostasis.

objectiveWe hypothesized that targeting early glutamatergic hyperexcitation through riluzole treatment could aid in attenuating co-occurring metabolic and amyloidogenic pathologies with the intent of ameliorating cognitive decline.

methodsWe conducted an early intervention study in male and female transgenic (AβPP/PS1) and knock-in (APPNL - F/NL - F) AD mice to assess the on- and off-treatment effects of prodromal glutamatergic modulation (2-6 months of age) on glucose homeostasis and spatial cognition through riluzole treatment.

resultsResults indicated a sex- and genotype-specific effect on glucose homeostasis and spatial cognition with riluzole intervention that evolved with disease progression and time since treatment.

conclusionThese findings support the interconnected nature of glucose and glutamatergic homeostasis with amyloid pathology and petition for further investigation into the targeting of this relationship to improve cognitive performance.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsCognitionDisease Models, AnimalFemaleGlucoseHomeostasisHumansMaleMiceMice, Inbred C57BLMice, TransgenicRiluzoleAmyloid beta-PeptidesAmyloid beta-Protein PrecursorGlucoseRiluzoleAlzheimer’s diseaseamyloidhippocampusinsulinlearningmemorymetabolism

Identifiers

PMID37248899
PMCPMC10357216
OpenAlexW4378363978

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.