Evidence map›Paper›PMID 24614170›Full record

ArticlePloS one2014

7,8-Dihydroxyflavone, a small molecule TrkB agonist, improves spatial memory and increases thin spine density in a mouse model of Alzheimer disease-like neuronal loss.

Nicholas A Castello, Michael H Nguyen, Jenny D Tran, David Cheng, Kim N Green, Frank M LaFerla

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
5.9field-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

71 citing papers in PubMed, 114 citations in OpenAlex.

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  11. Receptor-Independent Anti-Ferroptotic Activity of TrkB Modulators.International journal of molecular sciences · 2022
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  20. The TrkB agonist, 7,8-dihydroxyflavone, impairs fracture healing in mice.Journal of musculoskeletal & neuronal interactions · 2021
    Article

11 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

6 authors at 1 institution in 1 country.

Nicholas A CastelloInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
Michael H NguyenInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
Jenny D TranInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
David ChengInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
Kim N GreenInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
Frank M LaFerlaInstitute for Memory Impairments and Neurological Disorders, University of California Irvine, Irvine, California, United States of America; Department of Neurobiology and Behavior, University of California Irvine, Irvine, California, United States of America.
University of California, Irvine · US

Funding

Investigating the role of BDNF in the Stem Cell-mediated Restoration of CognitionF31AG034061 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI CASTELLO, NICHOLAS ALAN · 2009 to 2011
$103k
NIA NIH HHS F31 AG034061NIA NIH HHS F31AG034061
6 · The paper itself

Abstract

Augmenting BDNF/TrkB signaling has been demonstrated to be a promising strategy for reversing cognitive deficits in preclinical models of Alzheimer disease (AD). Although these studies highlight the potential of targeting BDNF/TrkB signaling, this strategy has not yet been tested in a model that develops the disease features that are most closely associated with cognitive decline in AD: severe synaptic and neuronal loss. In the present study, we investigated the impact of 7,8-dihydroxyflavone (DHF), a TrkB agonist, in CaM/Tet-DTA mice, an inducible model of severe neuronal loss in the hippocampus and cortex. Systemic 7,8-DHF treatment significantly improved spatial memory in lesioned mice, as measured by water maze. Analysis of GFP-labeled neurons in CaM/Tet-DTA mice revealed that 7,8-DHF induced a significant and selective increase in the density of thin spines in CA1 of lesioned mice, without affecting mushroom or stubby spines. These findings suggest chronic upregulation of TrkB signaling with 7,8-DHF may be an effective and practical strategy for improving function in AD, even after substantial neuronal loss has occurred.

Indexed as

Alzheimer DiseaseAnimalsCalmodulinDendritic SpinesDisease Models, AnimalFlavonesGreen Fluorescent ProteinsMiceNeuronsPyramidal CellsReceptor, trkBSpatial Memory6,7-dihydroxyflavoneCalmodulinFlavonesGreen Fluorescent ProteinsReceptor, trkB

Identifiers

PMID24614170
PMCPMC3948846
OpenAlexW2086492737

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.