Evidence map›Paper›PMID 24121970›Full record

ArticleJournal of Alzheimer's disease : JAD2014

Experimental induction of type 2 diabetes in aging-accelerated mice triggered Alzheimer-like pathology and memory deficits.

Jogender Mehla, Balwantsinh C Chauhan, Neelima B Chauhan

Open access · greenAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.7field-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

48 citing papers in PubMed, 92 citations in OpenAlex.

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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

3 authors at 3 institutions in 1 country.

Jogender MehlaNeuroscience Research, Jesse Brown VA Medical Center, Chicago, IL, USA Department of Pediatrics, University of Illinois Hospital & Health Science System-Children's Hospital, University of Illinois at Chicago, Chicago, IL, USA.
Balwantsinh C ChauhanDepartment of Biopharmaceutical Sciences, Roosevelt University, Schaumburg, IL, USA.
Neelima B ChauhanNeuroscience Research, Jesse Brown VA Medical Center, Chicago, IL, USA Department of Pediatrics, University of Illinois Hospital & Health Science System-Children's Hospital, University of Illinois at Chicago, Chicago, IL, USA.
Jesse Brown VA Medical Center · USRoosevelt University · USUniversity of Illinois Chicago · US

Funding

Therapeutic Efficacy of Intranasal WGA-GLP1 in ADR21NS079614 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHAUHAN, NEELIMA · 2013 to 2014
$437k
WGA as a Novel Vehicle for Intranasal Delivery of an Anti-A-beta Antibody in ADR21AG039625 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHAUHAN, NEELIMA · 2011 to 2012
$373k
Neuroregenerative Effects of Simvastatin in TBII01RX000880 · VA · JESSE BROWN VA MEDICAL CENTER · PI CHAUHAN, NEELIMA · 2015 to 2016
–
NIA NIH HHS AG039625NIA NIH HHS R21 AG039625NINDS NIH HHS NS079614NINDS NIH HHS R21 NS079614RRD VA I01 RX000880
6 · The paper itself

Abstract

Alzheimer's disease (AD) is an age-dependent neurodegenerative disease constituting ~95% of late-onset non-familial/sporadic AD, and only ~5% accounting for early-onset familial AD. Availability of a pertinent model representing sporadic AD is essential for testing candidate therapies. Emerging evidence indicates a causal link between diabetes and AD. People with diabetes are >1.5-fold more likely to develop AD. Senescence-accelerated mouse model (SAMP8) of accelerated aging displays many features occurring early in AD. Given the role played by diabetes in the pre-disposition of AD, and the utility of SAMP8 non-transgenic mouse model of accelerated aging, we examined if high fat diet-induced experimental type 2 diabetes in SAMP8 mice will trigger pathological aging of the brain. Results showed that compared to non-diabetic SAMP8 mice, diabetic SAMP8 mice exhibited increased cerebral amyloid-β, dysregulated tau-phosphorylating glycogen synthase kinase 3β, reduced synaptophysin immunoreactivity, and displayed memory deficits, indicating Alzheimer-like changes. High fat diet-induced type 2 diabetic SAMP8 mice may represent the metabolic model of AD.

Indexed as

AgingAlzheimer DiseaseAnimalsBrainDiabetes Mellitus, Type 2Dietary FatsDisease Models, AnimalMemory DisordersMiceMice, TransgenicSynaptophysintau ProteinsDietary FatsSynaptophysintau ProteinsAlzheimer's diseaseamyloid-βdiabetesglycogen synthase kinase-3βlearning and memorypathological aging of the brainsenescence-accelerated micesynaptophysintau

Identifiers

PMID24121970
PMCPMC3941701
OpenAlexW1657419816

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.