Evidence map›Paper›PMID 28736170›Full record

ArticleCurrent biology : CB2017

Overlap among Spatial Memories Triggers Repulsion of Hippocampal Representations.

Avi J H Chanales, Ashima Oza, Serra E Favila, Brice A Kuhl

Abstract read
In one paragraph

Article in Current biology : CB, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing 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

103 citing papers in PubMed.

  1. Hippocampal Mechanisms Support Cortisol-Induced Memory Enhancements.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  8. The hippocampus rapidly integrates sequence representations during novel multistep predictions.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Article
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  10. Medial temporal lobe encodes cognitive maps of real-world social networks.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  16. High coherence among training exemplars promotes broad generalization of face families.Journal of experimental psychology. Learning, memory, and cognition · 2025
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  17. Article
  18. A compressed code for memory discrimination.bioRxiv : the preprint server for biology · 2025
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  20. Maintenance suppression enhances subsequent associative learning.Proceedings of the National Academy of Sciences of the United States of America · 2025
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43 more citing papers are in PubMed but not listed here.

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

4 authors.

Avi J H ChanalesDepartment of Psychology, New York University, 6 Washington Place, New York, NY 10003, USA. Electronic address: avi.chanales@nyu.edu.
Ashima OzaDepartment of Psychology, New York University, 6 Washington Place, New York, NY 10003, USA.
Serra E FavilaDepartment of Psychology, New York University, 6 Washington Place, New York, NY 10003, USA.
Brice A KuhlDepartment of Psychology and Institute of Neuroscience, 1227 University of Oregon, Eugene, OR 97403, USA. Electronic address: bkuhl@uoregon.edu.

Funding

Neural mechanisms for reducing interference during episodic memory formationR01NS089729 · NINDS · UNIVERSITY OF OREGON · PI KUHL, BRICE ALAN · 2014 to 2025
$3.8M
NINDS NIH HHS R01 NS089729
6 · The paper itself

Abstract

Across the domains of spatial navigation and episodic memory, the hippocampus is thought to play a critical role in disambiguating (pattern separating) representations of overlapping events. However, it is not fully understood how and why hippocampal patterns become separated. Here, we test the idea that event overlap triggers a "repulsion" among hippocampal representations that develops over the course of learning. Using a naturalistic route-learning paradigm and spatiotemporal pattern analysis of human fMRI data, we found that hippocampal representations of overlapping routes gradually diverged with learning to the point that they became less similar than representations of non-overlapping events. In other words, the hippocampus not only disambiguated overlapping events but formed representations that "reversed" the objective similarity among routes. This finding, which was selective to the hippocampus, is not predicted by standard theoretical accounts of pattern separation. Critically, because the overlapping route stimuli that we used ultimately diverged (so that each route contained overlapping and non-overlapping segments), we were able to test whether the reversal effect was selective to the overlapping segments. Indeed, once overlapping routes diverged (eliminating spatial and visual similarity), hippocampal representations paradoxically became relatively more similar. Finally, using a novel analysis approach, we show that the degree to which individual hippocampal voxels were initially shared across route representations was predictive of the magnitude of learning-related separation. Collectively, these findings indicate that event overlap triggers a repulsion of hippocampal representations-a finding that provides critical mechanistic insight into how and why hippocampal representations become separated.

Indexed as

Memory, EpisodicSpatial MemoryAdultFemaleHippocampusHumansMagnetic Resonance ImagingMaleYoung Adultepisodic memoryfMRIhippocampusmemory interferenceorthogonalizationpattern separationrepresentational similarityspatial navigation

Identifiers

PMID28736170
PMCPMC5576038

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Registered trials

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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.