Evidence map›Paper›PMID 36142737›Full record

ArticleInternational journal of molecular sciences2022

Investigation of Anxiety- and Depressive-like Symptoms in 4- and 8-Month-Old Male Triple Transgenic Mouse Models of Alzheimer's Disease.

Dorottya Várkonyi, Bibiána Török, Eszter Sipos, Csilla Lea Fazekas, Krisztina Bánrévi, Pedro Correia, Tiago Chaves, Szidónia Farkas, Adrienn Szabó, Sergio Martínez-Bellver and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.5field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

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  8. Neural substrates for regulating self-grooming behavior in rodents.Journal of Zhejiang University. Science. B · 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

12 authors at 4 institutions in 2 countries.

Dorottya VárkonyiCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Bibiána TörökCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Eszter SiposLaboratory of Behavioral and Stress Studies, Institute of Experimental Medicine, 1083 Budapest, Hungary.
Csilla Lea FazekasCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Krisztina BánréviLaboratory of Behavioral and Stress Studies, Institute of Experimental Medicine, 1083 Budapest, Hungary.
Pedro CorreiaCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Tiago ChavesCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Szidónia FarkasCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.ORCID 0000-0003-4239-4936
Adrienn SzabóCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
Sergio Martínez-BellverLendület Laboratory of Systems Neuroscience, Institute of Experimental Medicine, 1083 Budapest, Hungary.ORCID 0000-0001-8118-1517
Balázs HangyaLendület Laboratory of Systems Neuroscience, Institute of Experimental Medicine, 1083 Budapest, Hungary.ORCID 0000-0003-2709-7407
Dóra ZelenaCenter for Neuroscience, Szentágothai Research Center, Institute of Physiology, Medical School, University of Pécs, 7624 Pécs, Hungary.
HUN-REN Institute of Experimental Medicine · HUSemmelweis University · HUUniversitat de València · ESUniversity of Pecs · HU

Funding

National Research Development and Innovation Office of Hungary K141934, K138763 and K120311Thematic Excellence Program 2021 Health Sub-program of the Ministry for Innovation and Technology in Hungary TKP2021-EGA-16
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the most common form of dementia. Approximately 50% of AD patients show anxiety and depressive symptoms, which may contribute to cognitive decline. We aimed to investigate whether the triple-transgenic mouse (3xTg-AD) is a good preclinical model of this co-morbidity. The characteristic histological hallmarks are known to appear around 6-month; thus, 4- and 8-month-old male mice were compared with age-matched controls. A behavioral test battery was used to examine anxiety- (open field (OF), elevated plus maze, light-dark box, novelty suppressed feeding, and social interaction (SI) tests), and depression-like symptoms (forced swim test, tail suspension test, sucrose preference test, splash test, and learned helplessness) as well as the cognitive decline (Morris water maze (MWM) and social discrimination (SD) tests). Acetylcholinesterase histochemistry visualized cholinergic fibers in the cortex. Dexamethasone-test evaluated the glucocorticoid non-suppression. In the MWM, the 3xTg-AD mice found the platform later than controls in the 8-month-old cohort. The SD abilities of the 3xTg-AD mice were missing at both ages. In OF, both age groups of 3xTg-AD mice moved significantly less than the controls. During SI, 8-month-old 3xTg-AD animals spent less time with friendly social behavior than the controls. In the splash test, 3xTg-AD mice groomed themselves significantly less than controls of both ages. Cortical fiber density was lower in 8-month-old 3xTg-AD mice compared to the control. Dexamethasone non-suppression was detectable in the 4-month-old group. All in all, some anxiety- and depressive-like symptoms were present in 3xTg-AD mice. Although this strain was not generally more anxious or depressed, some aspects of comorbidity might be studied in selected tests, which may help to develop new possible treatments.

Indexed as

Alzheimer DiseaseAcetylcholinesteraseAnimalsAnxietyDexamethasoneDisease Models, AnimalGlucocorticoidsHumansMaleMiceMice, Inbred C57BLMice, TransgenicSucrosetau ProteinsAcetylcholinesteraseDexamethasoneGlucocorticoidsSucrosetau Proteins3xTg-ADAlzheimer’s disorderanxietydepressionmice models

Identifiers

PMID36142737
PMCPMC9501136
OpenAlexW4296449514

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.