Evidence map›Paper›PMID 25139992›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Interlamellar CA1 network in the hippocampus.

Sunggu Yang, Sungchil Yang, Thais Moreira, Gloria Hoffman, Greg C Carlson, Kevin J Bender, Bradley E Alger, Cha-Min Tang

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
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

52 citing papers in PubMed.

  1. Review
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  7. KThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  15. Increased Interhemispheric Connectivity of a Distinct Type of Hippocampal Pyramidal Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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  16. Article
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  18. Memory consolidation from a reinforcement learning perspective.Frontiers in computational neuroscience · 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

8 authors.

Sunggu YangDepartments of Neurology and.
Sungchil YangCenter for Integrative Neuroscience, Department of Neurology, University of California, San Francisco, CA 94608;
Thais MoreiraDepartments of Neurology and.
Gloria HoffmanDepartment of Biology, Morgan State University, Baltimore, MD 21251;
Greg C CarlsonCenter for Neurobiology and Behavior, University of Pennsylvania, Philadelpia, PA 19104-3403.
Kevin J BenderCenter for Integrative Neuroscience, Department of Neurology, University of California, San Francisco, CA 94608;
Bradley E AlgerPhysiology, University of Maryland School of Medicine, Baltimore, MD 21201;
Cha-Min TangDepartments of Neurology and Physiology, University of Maryland School of Medicine, Baltimore, MD 21201; Baltimore Veterans Affairs Medical Center, Baltimore, MD 21201; and ctang@som.umaryland.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To understand the cellular basis of learning and memory, the neurophysiology of the hippocampus has been largely examined in thin transverse slice preparations. However, the synaptic architecture along the longitudinal septo-temporal axis perpendicular to the transverse projections in CA1 is largely unknown, despite its potential significance for understanding the information processing carried out by the hippocampus. Here, using a battery of powerful techniques, including 3D digital holography and focal glutamate uncaging, voltage-sensitive dye, two-photon imaging, electrophysiology, and immunohistochemistry, we show that CA1 pyramidal neurons are connected to one another in an associational and well-organized fashion along the longitudinal axis of the hippocampus. Such CA1 longitudinal connections mediate reliable signal transfer among the pyramidal cells and express significant synaptic plasticity. These results illustrate a need to reconceptualize hippocampal CA1 network function to include not only processing in the transverse plane, but also operations made possible by the longitudinal network. Our data will thus provide an essential basis for future computational modeling studies on information processing operations carried out in the full 3D hippocampal network that underlies its complex cognitive functions.

Indexed as

AnimalsBrain MappingCA1 Region, HippocampalCA3 Region, HippocampalDendritesDentate GyrusLong-Term PotentiationMemory, Short-TermMiceMice, Inbred C57BLNeural PathwaysNeuronal PlasticityPyramidal CellsRatsRats, Sprague-DawleySynaptic PotentialsCA1 association fibersDHRlongitudinal axonssequence memory

Identifiers

PMID25139992
PMCPMC4156755

What OpenQuestion holds

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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.