Evidence map›Paper›PMID 27265785›Full record

ArticleBehavioural brain research2017

Hippocampal proteomics defines pathways associated with memory decline and resilience in normal aging and Alzheimer's disease mouse models.

Sarah M Neuner, Lynda A Wilmott, Brian R Hoffmann, Khyobeni Mozhui, Catherine C Kaczorowski

Open access · hybridAbstract read
In one paragraph

Article in Behavioural brain research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.3field-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

58 citing papers in PubMed, 96 citations in OpenAlex.

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  11. Whole-genome sequencing study in Koreans identifies novel loci for Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
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  20. High-Contrast PET Imaging with [Journal of medicinal chemistry · 2023
    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 2 institutions in 1 country.

Sarah M NeunerDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, United States.
Lynda A WilmottDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, United States.
Brian R HoffmannDepartment of Medicine, Division of Cardiology and Biotechnology and Bioengineering Center, Medical College of Wisconsin, Milwaukee, WI, 53226 United States.
Khyobeni MozhuiDepartment of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, United States.
Catherine C KaczorowskiDepartment of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, United States. Electronic address: ckaczoro@uthsc.edu.
University of Tennessee Health Science Center · USMedical College of Wisconsin · US

Funding

Proteomics of memory failure: unraveling the relationship between 'normal' brainR00AG039511 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KACZOROWSKI, CATHERINE COOK · 2013 to 2015
$730k
Mapping AD Memory Failure: Molecules to Connectivity of Brain NetworkR21AG048446 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KACZOROWSKI, CATHERINE COOK · 2015 to 2016
$418k
Identification of Genetic Modifiers of Neuronal Deficits and Memory Failure in Alzheimers DiseaseF31AG050357 · NIA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI NEUNER, SARAH M · 2015 to 2018
$171k
Proteomics of memory: Normal brain aging and Alzheimers DiseaseK99AG039511 · NIA · MEDICAL COLLEGE OF WISCONSIN · PI KACZOROWSKI, CATHERINE COOK · 2012 to 2013
$105k
NIA NIH HHS F31 AG050357NIA NIH HHS K99 AG039511NIA NIH HHS R00 AG039511NIA NIH HHS R21 AG048446
6 · The paper itself

Abstract

Alzheimer's disease (AD), the most common form of dementia in the elderly, has no cure. Thus, the identification of key molecular mediators of cognitive decline in AD remains a top priority. As aging is the most significant risk factor for AD, the goal of this study was to identify altered proteins and pathways associated with the development of normal aging and AD memory deficits, and identify unique proteins and pathways that may contribute to AD-specific symptoms. We used contextual fear conditioning to diagnose 8-month-old 5XFAD and non-transgenic (Ntg) mice as having either intact or impaired memory, followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) to quantify hippocampal membrane proteins across groups. Subsequent analysis detected 113 proteins differentially expressed relative to memory status (intact vs impaired) in Ntg mice and 103 proteins in 5XFAD mice. Thirty-six proteins, including several involved in neuronal excitability and synaptic plasticity (e.g., GRIA1, GRM3, and SYN1), were altered in both normal aging and AD. Pathway analysis highlighted HDAC4 as a regulator of observed protein changes in both genotypes and identified the REST epigenetic regulatory pathway and G

Indexed as

ProteomeAgingAlzheimer DiseaseAmyloid beta-Protein PrecursorAnimalsChromatography, LiquidConditioning, PsychologicalDisease Models, AnimalFearHippocampusHumansMemoryMemory DisordersMice, TransgenicPresenilin-1ProteomicsAmyloid beta-Protein PrecursorAPP protein, humanPresenilin-1ProteomePSEN1 protein, humanAgingAlzheimer’s diseaseCognitionIon channelsProteomics

Identifiers

PMID27265785
PMCPMC5135662
OpenAlexW2413377811

What OpenQuestion holds

Textmetadata
LicenceTDM
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.