Evidence map›Paper›PMID 41072851›Full record

ArticleBehavioural brain research2026

Time-restricted feeding in adult mice improves mood-related behaviors in a sex-dependent manner.

Kiersten S Bell, Jeffrey S Darling, Akshay Prabhakar, Shams T Imad, Andrew D Gaudet, Laura K Fonken

Abstract read
In one paragraph

Article in Behavioural brain research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Kiersten S BellDivision of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
Jeffrey S DarlingDivision of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
Akshay PrabhakarDivision of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
Shams T ImadDivision of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
Andrew D GaudetDepartment of Psychology, University of Texas at Austin, USA; Department of Neurology, University of Texas at Austin, USA.
Laura K FonkenDivision of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA. Electronic address: laura.fonken@austin.utexas.edu.

Funding

Disrupted Circadian Regulation of Cell Migration at CNS-Immune Interfaces in Aging and Alzheimer's DiseaseR01AG078758 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI Laura K Fonken · 2022 to 2026
$2.9M
The influence of the developing circadian system on neuroimmune function and neuropsychiatric behaviorsF31MH138131 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI BELL, KIERSTEN SIMONE · 2024 to 2025
$82k
NIA NIH HHS R01 AG078758NIMH NIH HHS F31 MH138131
6 · The paper itself

Abstract

Time-restricted feeding (TRF), which limits food intake to specific time windows, protects against metabolic dysfunction and inflammation. Given TRF's potential benefits, it has been increasingly adopted as a simple dietary intervention. However, limited work has explored whether TRF impacts brain and behavior, and whether its effects are sex-dependent. Since brain inflammation can regulate mood-related behaviors, we hypothesized that TRF would dampen neuroimmune reactivity and protect against associated behavioral changes in adult mice. To test this, male and female mice were either fed during their active (dark) phase for 10 h (TRF) or had unrestricted access to food throughout the day (ad libitum). After five weeks, TRF reduced anxiety-like behaviors in an open field task and in the elevated plus maze in both sexes. TRF females also showed greater sociability in a social exploration task. Next, mice were injected with lipopolysaccharide (LPS) or saline to determine whether TRF protects against impairments in mood elicited by an immune challenge. 24 h post administration, TRF rescued LPS-induced behavioral despair in females but not males. TRF also attenuated LPS-induced hippocampal expression of pro-inflammatory cytokines and some morphological changes in microglia, the brain's immune cell. These findings suggest TRF exerts sex-specific effects on behaviors and neuroimmune functions. Overall, adult female mice were more sensitive to TRF, with greater behavioral and neuroimmune changes than males.

Indexed as

AffectAnxietyBehavior, AnimalFastingSex CharacteristicsAnimalsFemaleHippocampusLipopolysaccharidesMaleMiceMice, Inbred C57BLSex FactorsSocial BehaviorLipopolysaccharidesAnxietyBehaviorDepressionLipopolysaccharideSex differenceTime-restricted feeding

Identifiers

PMID41072851
PMCPMC12983346

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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.