Evidence map›Paper›PMID 40032133›Full record

ArticleNeurobiology of learning and memory2025

Developmental changes in brain-wide fear memory networks.

Benita Jin, Michael W Gongwer, Laura A DeNardo

Abstract read
In one paragraph

Article in Neurobiology of learning and memory, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Maternal experience alters brain-wide representation of infant cries.bioRxiv : the preprint server for biology · 2026
    Article
  2. Review
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

3 authors.

Benita JinDepartment of Physiology, University of California, Los Angeles, 650 Charles E Young Dr S, Los Angeles, CA 90095, USA; Program in Molecular, Cellular and Integrative Physiology, University of California, Los Angeles, Los Angeles, CA, USA.
Michael W GongwerDepartment of Physiology, University of California, Los Angeles, 650 Charles E Young Dr S, Los Angeles, CA 90095, USA; Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, CA, USA; Medical Scientist Training Program, University of California, Los Angeles, Los Angeles, CA, USA.
Laura A DeNardoDepartment of Physiology, University of California, Los Angeles, 650 Charles E Young Dr S, Los Angeles, CA 90095, USA. Electronic address: ldenardo@ucla.edu.

Funding

UCLA-Caltech Medical Scientist Training ProgramT32GM008042 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AJIJOLA, OLUJIMI A, DAWSON, DAVID WAYNE · 1985 to 2023
$29.9M
Training Grant in Neurobehavioral GeneticsT32NS048004 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BEARDEN, CARRIE E, OPHOFF, ROEL A · 2004 to 2025
$5.8M
Prefrontal circuits underlying the maturation of learned avoidanceR01MH127214 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Laura Anne DeNardo · 2022 to 2026
$2.3M
Role of prefrontal dopamine circuits in threat avoidance learningR01MH137461 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Laura Anne DeNardo, Scott Allen Wilke · 2024 to 2026
$2.2M
Examination of the Functional Role of Sca1+ Vascular Progenitor Cells following Vascular InjuryF32HL129651 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHULDT, ADAM J.T. · 2016 to 2017
$134k
Investigating circuit-specific effects of high-frequency repetitive transcranial magnetic stimulationF30MH134633 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GONGWER, MICHAEL W. · 2023 to 2024
$81k
NHLBI NIH HHS F32 HL129651NIGMS NIH HHS T32 GM008042NIMH NIH HHS F30 MH134633NIMH NIH HHS R01 MH127214NIMH NIH HHS R01 MH137461NINDS NIH HHS T32 NS048004
6 · The paper itself

Abstract

Memory retrieval involves coordinated activity across multiple brain regions. Yet how the organization of memory networks evolves throughout development remains poorly understood. In this study, we compared whole-brain functional networks that are active during contextual fear memory recall in infant, juvenile, and adult mice. Our analyses revealed that long-term memory networks change significantly across postnatal development. Infant fear memory networks are dense and heterogeneous, whereas adult networks are sparse and have a small-world topology. While hippocampal subregions were highly connected nodes at all ages, the cortex gained many functional connections across development. Different functional connections matured at different rates, but their developmental timing fell into three major categories: stepwise change between two ages, linear change across all ages, or inverted-U, with elevated functional connectivity in juveniles. Our work highlights how a subset of brain regions likely maintain important roles in fear memory encoding, but the functional connectivity of fear memory networks undergoes significant reorganization across development. Together, these results provide a blueprint for studying how correlated cellular activity in key areas distinctly regulates memory storage and retrieval across development.

Indexed as

BrainFearHippocampusMemoryMemory, Long-TermMental RecallNerve NetAnimalsFemaleMaleMiceMice, Inbred C57BLNeural PathwaysBrain-wide networksDevelopmentEpisodic MemoryFear conditioningInfantile AmnesiaMice

Identifiers

PMID40032133
PMCPMC12866929

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.