Evidence map›Paper›PMID 40316419›Full record

ArticleLearning & memory (Cold Spring Harbor, N.Y.)2025

The role of the parahippocampal cortex in memory consolidation for scenes.

Weizhen Xie, Susan G Wardle, Jenna Langbein, Oceane Fruchet, Molly Baumhauer, Audrey Phan, Ai Phuong Tong, Shruti Japee, Sara K Inati, Chris I Baker and 1 more

Abstract readCase Reports
In one paragraph

Article in Learning & memory (Cold Spring Harbor, N.Y.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

11 authors.

Weizhen XieDepartment of Psychology, University of Maryland, College Park, Maryland 20742, USA zanexie@umd.edu bakerchris@mail.nih.gov kareem.zaghloul@nih.gov.ORCID http://orcid.org/0000-0003-4655-6496
Susan G WardleLaboratory of Brain and Cognition, NIMH, National Institutes of Health, Bethesda, Maryland 20892, USA.ORCID http://orcid.org/0000-0003-2216-7461
Jenna LangbeinDepartment of Neurosurgery, University of Maryland, Baltimore, Maryland 21201, USA.
Oceane FruchetSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Molly BaumhauerSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Audrey PhanSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Ai Phuong TongSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Shruti JapeeLaboratory of Brain and Cognition, NIMH, National Institutes of Health, Bethesda, Maryland 20892, USA.
Sara K InatiSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Chris I BakerLaboratory of Brain and Cognition, NIMH, National Institutes of Health, Bethesda, Maryland 20892, USA zanexie@umd.edu bakerchris@mail.nih.gov kareem.zaghloul@nih.gov.
Kareem A ZaghloulSurgical Neurology Branch, NINDS, National Institutes of Health, Bethesda, Maryland 20892, USA zanexie@umd.edu bakerchris@mail.nih.gov kareem.zaghloul@nih.gov.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classic models propose that forming lasting visual memories involves coordinated interactions between visually selective neocortical structures and the hippocampus during memory consolidation. However, the precise role of visually selective neocortical structures in memory consolidation remains elusive, given their potential contributions spanning from initial perceptual encoding to subsequent memory reactivation. We capitalized on a unique opportunity, involving direct recording from the posterior parahippocampus and its subsequent resection in a neurological patient, to investigate the impact of scene-selective neocortical lesions on visual memory consolidation. First, with intracranial EEG, we confirmed the functional relevance of the patient's resected tissues in representing a specific visual category, in this case, scene images. Subsequently, we identified disruption of memory for scenes relative to faces and objects during the participant's postoperative visit. This finding prompted a comprehensive analysis of visual memory across different visual categories in this participant, as well as an examination of similar functions in other neurological patients with intact parahippocampi and a cohort of online participants. Through these within- and between-participant comparisons, we identified greater time-dependent reduction in visual memory for scene images following the resection of the posterior parahippocampus. Importantly, these changes in memory retention could not be attributed to a general reduction in initial memory encoding following neocortical lesions. Our findings, therefore, suggest that reactivating scene-selective neocortical areas is essential for converting transient visual perceptual experiences into lasting long-term scene memories.

Indexed as

Memory ConsolidationParahippocampal GyrusPattern Recognition, VisualVisual PerceptionElectrocorticographyHumans

Identifiers

PMID40316419
PMCPMC12052091

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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.