Evidence map›Paper›PMID 31960628›Full record

ArticleBrain and behavior2020

Intranasal deferoxamine can improve memory in healthy C57 mice, suggesting a partially non-disease-specific pathway of functional neurologic improvement.

Jared M Fine, Jacob Kosyakovsky, Amanda M Baillargeon, Julian V Tokarev, Jacob M Cooner, Aleta L Svitak, Katherine A Faltesek, William H Frey, Leah R Hanson

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  5. The Contribution of Type 2 Diabetes to Parkinson's Disease Aetiology.International journal of molecular sciences · 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.

Jared M FineNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.ORCID 0000-0002-0271-9065
Jacob KosyakovskyNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
Amanda M BaillargeonNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
Julian V TokarevNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
Jacob M CoonerNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
Aleta L SvitakNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
Katherine A FaltesekNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.
William H FreyNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.ORCID 0000-0002-6373-0794
Leah R HansonNeuroscience Research at HealthPartners Institute, Saint Paul, MN, USA.ORCID 0000-0002-2847-7949
HealthPartners · US

Funding

Center for Memory & Aging at HealthPartners Institute
6 · The paper itself

Abstract

introductionIntranasal deferoxamine (IN DFO) has been shown to decrease memory loss and have beneficial impacts across several models of neurologic disease and injury, including rodent models of Alzheimer's and Parkinson's disease.

methodsIn order to assess the mechanism of DFO, determine its ability to improve memory from baseline in the absence of a diseased state, and assess targeting ability of intranasal delivery, we treated healthy mice with IN DFO (2.4 mg) or intraperitoneal (IP) DFO and compared behavioral and biochemical changes with saline-treated controls. Mice were treated 5 days/week for 4 weeks and subjected to behavioral tests 30 min after dosing.

resultsWe found that IN DFO, but not IP DFO, significantly enhanced working memory in the radial arm water maze, suggesting that IN administration is more efficacious as a targeted delivery route to the brain. Moreover, the ability of DFO to improve memory from baseline in healthy mice suggests a non-disease-specific mechanism of memory improvement. IN DFO treatment was accompanied by decreased GSK-3β activity and increased HIF-1α activity.

conclusionsThese pathways are suspected in DFO's ability to improve memory and perhaps represent a component of the common mechanism through which DFO enacts beneficial change in models of neurologic disease and injury.

Indexed as

Administration, IntranasalAnimalsBrainDeferoxamineGlycogen Synthase Kinase 3 betaHypoxia-Inducible Factor 1, alpha SubunitMaleMemory, Short-TermMiceSiderophoresDeferoxamineGlycogen Synthase Kinase 3 betaHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitSiderophoresdeferoxamineglycogen synthase kinase 3βhypoxia-inducible factor 1αintranasalmemory enhancementradial arm water maze

Identifiers

PMID31960628
PMCPMC7066355
OpenAlexW3001604987

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.