Evidence map›Paper›PMID 26868479›Full record

ArticleNeurobiology of learning and memory2016

Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory.

Jessica H Hall, Frances K Wiseman, Elizabeth M C Fisher, Victor L J Tybulewicz, John L Harwood, Mark A Good

Open access · hybridAbstract read
In one paragraph

Article in Neurobiology of learning and memory, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Mouse models of aneuploidy to understand chromosome disorders.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Review
  4. Article
  5. Article
  6. Activation of the miR-34a-Mediated SIRT1/mTOR Signaling Pathway by Urolithin A Attenuates D-Galactose-Induced Brain Aging in Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Article
  7. Article
  8. Review
  9. Article
  10. Review
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 3 institutions in 1 country.

Jessica H HallSchool of Psychology, Cardiff University, CF10 3AT, UK.
Frances K WisemanDepartment of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Elizabeth M C FisherDepartment of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Victor L J TybulewiczFrancis Crick Institute, The Ridgeway, Mill Hill, London NW7 1AA, UK; Imperial College, London W12 0NN, UK.
John L HarwoodSchool of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Mark A GoodSchool of Psychology, Cardiff University, CF10 3AT, UK. Electronic address: Good@cardiff.ac.uk.
Cardiff University · GBUniversity College London · GBThe Francis Crick Institute · GB

Funding

Alzheimer's Society 192Medical Research Council G0601056Medical Research Council U117527252Wellcome Trust 080174Wellcome Trust 098327Wellcome Trust 098328
6 · The paper itself

Abstract

The present study examined memory function in Tc1 mice, a transchromosomic model of Down syndrome (DS). Tc1 mice demonstrated an unusual delay-dependent deficit in recognition memory. More specifically, Tc1 mice showed intact immediate (30sec), impaired short-term (10-min) and intact long-term (24-h) memory for objects. A similar pattern was observed for olfactory stimuli, confirming the generality of the pattern across sensory modalities. The specificity of the behavioural deficits in Tc1 mice was confirmed using APP overexpressing mice that showed the opposite pattern of object memory deficits. In contrast to object memory, Tc1 mice showed no deficit in either immediate or long-term memory for object-in-place information. Similarly, Tc1 mice showed no deficit in short-term memory for object-location information. The latter result indicates that Tc1 mice were able to detect and react to spatial novelty at the same delay interval that was sensitive to an object novelty recognition impairment. These results demonstrate (1) that novelty detection per se and (2) the encoding of visuo-spatial information was not disrupted in adult Tc1 mice. The authors conclude that the task specific nature of the short-term recognition memory deficit suggests that the trisomy of genes on human chromosome 21 in Tc1 mice impacts on (perirhinal) cortical systems supporting short-term object and olfactory recognition memory.

Indexed as

AnimalsDisease Models, AnimalDown SyndromeExploratory BehaviorFemaleMaleMemory DisordersMemory, Long-TermMemory, Short-TermMiceRecognition, PsychologySpatial BehaviorMemoryPerirhinalRecognitionSpatialTc1Trisomy-21

Identifiers

PMID26868479
PMCPMC4898594
OpenAlexW2258704607

What OpenQuestion holds

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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.