Evidence map›Paper›PMID 35597233›Full record

ArticleCurrent biology : CB2022

Loss of functional heterogeneity along the CA3 transverse axis in aging.

Heekyung Lee, Zitong Wang, Arjuna Tillekeratne, Nick Lukish, Vyash Puliyadi, Scott Zeger, Michela Gallagher, James J Knierim

Open access · greenAbstract read
In one paragraph

Article in Current biology : CB, 2022. 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
1.8field-weighted citation impact, top 16% 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, 16 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

8 authors at 2 institutions in 1 country.

Heekyung LeeKrieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD 21218, USA. Electronic address: heekyung@jhu.edu.
Zitong WangDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Arjuna TillekeratneKrieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD 21218, USA.
Nick LukishKrieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD 21218, USA.
Vyash PuliyadiKrieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, MD, USA.
Scott ZegerDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Michela GallagherDepartment of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, MD, USA; Kavli Neuroscience Discovery Institute, Johns Hopkins University, Baltimore, MD, USA.
James J KnierimKrieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD 21218, USA; Department of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, MD, USA; Kavli Neuroscience Discovery Institute, Johns Hopkins University, Baltimore, MD, USA; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. Electronic address: jknierim@jhu.edu.
Johns Hopkins University · USKennedy Krieger Institute · US

Funding

TRANSCRIPTIONAL MECHANISMS OF HIPPOCAMPAL AGINGP01AG009973 · NIA · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI JAMES J KNIERIM · 1991 to 2026
$52.4M
Research Training in Age-Related Cognitive DisordersT32AG027668 · NIA · JOHNS HOPKINS UNIVERSITY · PI MARILYN S. ALBERT · 2007 to 2026
$6.3M
NIA NIH HHS P01 AG009973NIA NIH HHS T32 AG027668
6 · The paper itself

Abstract

Age-related deficits in pattern separation have been postulated to bias the output of hippocampal memory processing toward pattern completion, which can cause deficits in accurate memory retrieval. Although the CA3 region of the hippocampus is often conceptualized as a homogeneous network involved in pattern completion, growing evidence demonstrates a functional gradient in CA3 along the transverse axis, as pattern-separated outputs (dominant in the more proximal CA3) transition to pattern-completed outputs (dominant in the more distal CA3). We examined the neural representations along the CA3 transverse axis in young (Y), aged memory-unimpaired (AU), and aged memory-impaired (AI) rats when different changes were made to the environment. Functional heterogeneity in CA3 was observed in Y and AU rats when the environmental similarity was high (altered cues or altered environment shapes in the same room), with more orthogonalized representations in proximal CA3 than in distal CA3. In contrast, AI rats showed reduced orthogonalization in proximal CA3 but showed normal (i.e., generalized) representations in distal CA3, with little evidence of a functional gradient. Under experimental conditions when the environmental similarity was low (different rooms), representations in proximal and distal CA3 remapped in all rats, showing that CA3 of AI rats is able to encode distinctive representations for inputs with greater dissimilarity. These experiments support the hypotheses that the age-related bias toward hippocampal pattern completion is due to the loss in AI rats of the normal transition from pattern separation to pattern completion along the CA3 transverse axis.

Indexed as

CA3 Region, HippocampalMemoryAgingAnimalsCuesHippocampusRatsagingCA3hippocampushyperactivitymemory impairmentpattern completionpattern separationplace cellsremapping

Identifiers

PMID35597233
PMCPMC9233142
OpenAlexW4282930920

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.