Evidence map›Paper›PMID 34958022›Full record

ArticleJournal of Alzheimer's disease : JAD2022

The Impact of the hAPP695SW Transgene and Associated Amyloid-β Accumulation on Murine Hippocampal Biochemical Pathways.

Mona Khorani, Gerd Bobe, Donald G Matthews, Armando Alcazar Magana, Maya Caruso, Nora E Gray, Joseph F Quinn, Jan F Stevens, Amala Soumyanath, Claudia S Maier

Open access · greenAbstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  5. Journal of Alzheimer's disease reports · 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

10 authors at 2 institutions in 1 country.

Mona KhoraniDepartment of Chemistry, Oregon State University, Corvallis, OR, USA.
Gerd BobeLinus Pauling Institute, Oregon State University, Corvallis, OR, USA.
Donald G MatthewsDepartment of Neurology, Oregon Health & Science University, Portland, OR, USA.
Armando Alcazar MaganaDepartment of Chemistry, Oregon State University, Corvallis, OR, USA.
Maya CarusoDepartment of Neurology, Oregon Health & Science University, Portland, OR, USA.
Nora E GrayDepartment of Neurology, Oregon Health & Science University, Portland, OR, USA.
Joseph F QuinnDepartment of Neurology, Oregon Health & Science University, Portland, OR, USA.
Jan F StevensLinus Pauling Institute, Oregon State University, Corvallis, OR, USA.
Amala SoumyanathDepartment of Neurology, Oregon Health & Science University, Portland, OR, USA.
Claudia S MaierDepartment of Chemistry, Oregon State University, Corvallis, OR, USA.
Oregon Health & Science University · USOregon State University · US

Funding

CAM Research Training in Neuroscience &StressT32AT002688 · NCCIH · OREGON HEALTH & SCIENCE UNIVERSITY · PI OKEN, BARRY S, SOUMYANATH, AMALA · 2005 to 2025
$7.2M
Mechanisms underlying the cognitive effects of Centella asiatica water extract and constituent compounds in the 5xFAD mouse model of Alzheimer's DiseaseU19AT010829 · NCCIH · OREGON HEALTH & SCIENCE UNIVERSITY · PI KRETZSCHMAR, DORIS · 2020 to 2024
$6.1M
Mechanisms and active compounds in the cognitive effects of Centella asiaticaR01AT008099 · NCCIH · OREGON HEALTH & SCIENCE UNIVERSITY · PI SOUMYANATH, AMALA · 2014 to 2018
$2.2M
Triple Quadrupole/Linear Ion Trap LC-MS/MS for LPIS10RR027878 · NCRR · OREGON STATE UNIVERSITY · PI STEVENS, JAN FREDERIK · 2010 to 2010
$484k
A novel estrogen modulator for the treatment of Alzheimer's diseaseI01BX003440 · VA · PORTLAND VA MEDICAL CENTER · PI QUINN, JOSEPH F · 2018 to 2021
–
BLRD VA I01 BX003440NCCIH NIH HHS R01 AT008099NCCIH NIH HHS T32 AT002688NCCIH NIH HHS U19 AT010829NCRR NIH HHS S10 RR027878
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a neurodegenerative disease characterized by the accumulation of amyloid-β (Aβ) peptide in the brain.

objectiveTo gain a better insight into alterations in major biochemical pathways underlying AD.

methodsWe compared metabolomic profiles of hippocampal tissue of 20-month-old female Tg2576 mice expressing the familial AD-associated hAPP695SW transgene with their 20-month-old wild type female littermates.

resultsThe hAPP695SW transgene causes overproduction and accumulation of Aβ in the brain. Out of 180 annotated metabolites, 54 metabolites differed (30 higher and 24 lower in Tg2576 versus wild-type hippocampal tissue) and were linked to the amino acid, nucleic acid, glycerophospholipid, ceramide, and fatty acid metabolism. Our results point to 1) heightened metabolic activity as indicated by higher levels of urea, enhanced fatty acid β-oxidation, and lower fatty acid levels; 2) enhanced redox regulation; and 3) an imbalance of neuro-excitatory and neuro-inhibitory metabolites in hippocampal tissue of aged hAPP695SW transgenic mice.

conclusionTaken together, our results suggest that dysregulation of multiple metabolic pathways associated with a concomitant shift to an excitatory-inhibitory imbalance are contributing mechanisms of AD-related pathology in the Tg2576 mouse.

Indexed as

MetabolomicsSignal TransductionAgedAlzheimer DiseaseAmyloid beta-PeptidesAnimalsBrainDisease Models, AnimalFemaleHippocampusHumansMiceMice, TransgenicTransgenesAmyloid beta-PeptidesAlzheimer’s diseaseexcitatory and inhibitory imbalancefatty acidshAPP695SWhippocampusmetabolomicsTg2576

Identifiers

PMID34958022
PMCPMC9584213
OpenAlexW4200037495

What Socratic 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 Socratic graph.