Evidence map›Paper›PMID 38045768›Full record

ArticleBiological psychiatry global open science2024

A New Behavioral Paradigm for Frustrative Nonreward in Juvenile Mice.

Aijaz Ahmad Naik, Xiaoyu Ma, Maxime Munyeshyaka, Ellen Leibenluft, Zheng Li

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Biological psychiatry global open science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06484088 (Characterizing the Brain Circuitry and Neural Activity Mediating Frustration), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
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.

NCT06484088 early_phase1recruitingnot on this mapstarted 2025, after this paper: background citation

Characterizing the Brain Circuitry and Neural Activity Mediating Frustration

TypeinterventionalSponsorNational Institute of Mental Health (NIMH)Ran2025 to 2027Enrolled90ConditionsIrritabilityArmsFrustration task
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Frustrative Nonreward: Behavior, Circuits, Neurochemistry, and Disorders.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  6. Irritability in Youths: A Critical Integrative Review.The American journal of psychiatry · 2024
    Review
  7. A New Paradigm to Investigate the Neuroscience of Irritability in Youth.Biological psychiatry global open science · 2024
    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

5 authors at 1 institution in 1 country.

Aijaz Ahmad NaikSection on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
Xiaoyu MaSection on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
Maxime MunyeshyakaSection on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
Ellen LeibenluftSection on Mood Dysregulation and Neuroscience, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
Zheng LiSection on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland.
National Institutes of Health · US

Funding

The Pathophysiology and Treatment Of Children With Severe Mood DysregulationZIAMH002786 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEIBENLUFT, ELLEN · 2009 to 2023
$34.0M
Non-apoptotic function of casapses in synapsesZIAMH002881 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LI, ZHENG · 2009 to 2025
$18.9M
Intramural NIH HHS ZIA MH002786Intramural NIH HHS ZIA MH002881
6 · The paper itself

Abstract

Background: Irritability, defined as proneness to anger, can reach a pathological extent. It is a defining symptom of disruptive mood dysregulation disorder and one of the most common reasons youths present for psychiatric evaluation and care. Aberrant responses to frustrative nonreward (FNR), the response to omission of expected reward, are central to the pathophysiology of irritability. FNR is a translational construct to study irritability across species. The development of preclinical FNR models would advance mechanistic studies of the important and relatively understudied clinical phenomenon of irritability. Methods: We used FNR as a conceptual framework to develop a novel mouse behavioral paradigm named alternate poking reward omission. Juvenile mice were exposed to alternate poking reward omission and then examined with a battery of behavioral tests to determine the behavioral effect of FNR. Results: FNR increased locomotion and aggression regardless of sex. These behavioral changes elicited by FNR resemble the symptoms observed in youth with severe irritability. FNR had no effect on anxiety-like, depression-like, or nonaggressive social behaviors. Conclusions: Our alternate poking reward omission paradigm effectively elevated aggression and locomotion in juvenile mice. These frustration effects are directly related to behavioral symptoms of youth with severe irritability. Our novel behavioral paradigm lays the groundwork for further mechanistic studies of frustration and irritability in rodents.

Indexed as

AggressionDMDDFrustrative nonrewardHyperlocomotionIrritability

Identifiers

PMID38045768
PMCPMC10689275
OpenAlexW4388779019

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.