Evidence map›Paper›PMID 28686801›Full record

ArticleHippocampus2017

Exposure to complex environments results in more sparse representations of space in the hippocampus.

David K Bilkey, Kirsten R Cheyne, Michael J Eckert, Xiaodong Lu, Shoaib Chowdhury, Paul F Worley, James E Crandall, Wickliffe C Abraham

Open access · greenAbstract read
In one paragraph

Article in Hippocampus, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

14 citing papers in PubMed, 21 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 3 institutions in 2 countries.

David K BilkeyDepartment of Psychology and the Brain Health Research Centre, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-1256-4888
Kirsten R CheyneDepartment of Psychology and the Brain Health Research Centre, University of Otago, Dunedin, New Zealand.
Michael J EckertDepartment of Psychology and the Brain Health Research Centre, University of Otago, Dunedin, New Zealand.
Xiaodong LuDepartment of Psychology and the Brain Health Research Centre, University of Otago, Dunedin, New Zealand.
Shoaib ChowdhuryThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.
Paul F WorleyThe Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205.
James E CrandallEunice Kennedy Shriver Center, University of Massachusetts Medical School, Waltham, Massachusetts, 02452.
Wickliffe C AbrahamDepartment of Psychology and the Brain Health Research Centre, University of Otago, Dunedin, New Zealand.
Brain Research New Zealand · NZJohns Hopkins University · USUniversity of Massachusetts Chan Medical School · US

Funding

NOVEL CELLULAR MECHANISMS IN CORTEX DEVELOPMENTR01MH053608 · NIMH · JOHNS HOPKINS UNIVERSITY · PI WORLEY, PAUL F · 1994 to 2024
$9.3M
De novo Synthesis and MemoryR35NS097966 · NINDS · JOHNS HOPKINS UNIVERSITY · PI WORLEY, PAUL F · 2017 to 2024
$4.3M
NIMH NIH HHS R01 MH053608NINDS NIH HHS R35 NS097966
6 · The paper itself

Abstract

The neural circuitry mediating sensory and motor representations is adaptively tuned by an animal's interaction with its environment. Similarly, higher order representations such as spatial memories can be modified by exposure to a complex environment (CE), but in this case the changes in brain circuitry that mediate the effect are less well understood. Here, we show that prolonged CE exposure was associated with increased selectivity of CA1 "place cells" to a particular recording arena compared to a social control (SC) group. Furthermore, fewer CA1 and DG neurons in the CE group expressed high levels of Arc protein, a marker of recent activation, following brief exposure to a completely novel environment. The reduced Arc expression was not attributable to overall changes in cell density or number. These data indicate that one effect of CE exposure is to modify high-level spatial representations in the brain by increasing the sparsity of population coding within networks of neurons. Greater sparsity could result in a more efficient and compact coding system that might alter behavioural performance on spatial tasks. The results from a behavioural experiment were consistent with this hypothesis, as CE-treated animals habituated more rapidly to a novel environment despite showing equivalent initial responding.

Indexed as

EnvironmentAction PotentialsAnimalsCytoskeletal ProteinsElectrodes, ImplantedExploratory BehaviorHippocampusImmunohistochemistryMaleMicroscopy, ConfocalNerve Tissue ProteinsPlace CellsRandom AllocationRats, Sprague-DawleySpace PerceptionSpatial Behavioractivity regulated cytoskeletal-associated proteinCytoskeletal ProteinsNerve Tissue Proteinsenriched environmentimmediate early geneplace cellsparsityspatial representation

Identifiers

PMID28686801
PMCPMC5752118
OpenAlexW2728960587

What OpenQuestion holds

Textmetadata
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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.