Evidence map›Paper›PMID 34748926›Full record

ArticleNeurobiology of learning and memory2021

Extinction trial spacing across days differentially impacts fear regulation in adult and adolescent male mice.

Danielle M Gerhard, Heidi C Meyer

Abstract read
In one paragraph

Article in Neurobiology of learning and memory, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Developmental Shifts in Amygdala Function.Current topics in behavioral neurosciences · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. The impact of temporal distribution on fear extinction learning.International journal of clinical and health psychology : IJCHP
    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

2 authors.

Danielle M GerhardDepartment of Psychiatry, Weill Cornell Medicine, New York, NY, United States. Electronic address: dmg2005@med.cornell.edu.
Heidi C MeyerDepartment of Psychiatry, Weill Cornell Medicine, New York, NY, United States; Department of Psychological and Brain Sciences, Boston University, Boston, MA, United States. Electronic address: hcmeyer@bu.edu.

Funding

J. NRSA Training CoreTL1TR002386 · NCATS · WEILL MEDICAL COLL OF CORNELL UNIV · PI Genevieve Giny Fouda Amou ou · 2017 to 2026
$5.8M
The Impact of the BDNF Val66Met Prodomain on Cognitive Function in a Mouse Model of Alzheimer's DiseaseR01NS052819 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HEMPSTEAD, BARBARA L, LEE, FRANCIS SANG YONG · 2005 to 2019
$5.3M
Developmental Engagement of Neural Circuitry Underlying Safety LearningR00MH119320 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MEYER, HEIDI CATHERINE · 2022 to 2024
$747k
Developmental engagement of neural circuitry underlying safety learningK99MH119320 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI MEYER, HEIDI CATHERINE · 2019 to 2020
$174k
NCATS NIH HHS TL1 TR002386NIMH NIH HHS K99 MH119320NIMH NIH HHS R00 MH119320NINDS NIH HHS R01 NS052819
6 · The paper itself

Abstract

Fear regulation changes as a function of age and adolescence is a key developmental period for the continued maturation of fear neural circuitry. A consistent finding in the literature is diminished extinction retention in adolescents. However, these studies often directly compare adolescents to adults using a single protocol and therefore provide little insight into learning parameters that improve adolescent fear regulation. Studies in adults highlight the benefits of spaced learning over massed learning. These findings have been extended to fear regulation, with adult rodents exhibiting improved extinction learning and retention when cues are distributed over days versus a single session. However, similar studies have not been performed in adolescents. Here, we systematically examine the impact of trial spacing across days on fear regulation. Adolescent or adult male mice were exposed to one of three extinction paradigms that presented the same number of trials but differed in the temporal distribution of trials across days (one day, two days, or four days). We found that introducing consolidation events into the protocol improves adult extinction learning and short-term extinction retention but these effects disappear after two weeks. For adolescents, all three protocols were comparably effective in reducing freezing across extinction training and improved retention at both short-term and long-term fear recall time points relative to extinction-naive mice. These findings suggest that extinction protocols that incorporate consolidation events are optimal for adults but additional booster training may be required for enduring efficacy. In contrast, protocols incorporating either massed or spaced presentations show immediate and enduring benefits for adolescents.

Indexed as

AnimalsExtinction, PsychologicalFearLearningMaleMiceTime FactorsAdolescenceConsolidationFear extinctionMassed learningMemorySpaced learning

Identifiers

PMID34748926
PMCPMC8744067

What OpenQuestion holds

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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.