Evidence map›Paper›PMID 41933815›Full record

ArticleThe journal of pain2026

High-resolution metabolic profiling of the effects of early-life stress after peripheral nerve injury.

Kayleigh A Rodriguez, Mary Grace Bishop, Laura R Osborn, Dakota Redling, James D Sikes, Craig Porter, Laxmi Yeruva, Kimberly E Stephens

Abstract read
In one paragraph

Article in The journal of pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Kayleigh A RodriguezArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Neuroscience, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 847, Little Rock, AR 72205, United States.
Mary Grace BishopArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Neuroscience, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 847, Little Rock, AR 72205, United States.
Laura R OsbornArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Neuroscience, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 847, Little Rock, AR 72205, United States.
Dakota RedlingArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Neuroscience, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 847, Little Rock, AR 72205, United States.
James D SikesArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States.
Craig PorterArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Pediatrics, College of Medicine, University of Arkansas for Medical Sciences, 3 Children's Way, Little Rock, AR 72202, United States.
Laxmi YeruvaMicrobiome and Metabolism Research Unit, Arkansas Children's Nutrition Center, US Department of Agriculture, Agricultural Research Service, 15 Childrens Way, Little Rock, AR 72202, United States.
Kimberly E StephensArkansas Children's Research Institute, 13 Children's Way, Little Rock, AR 72202, United States; Department of Neuroscience, College of Medicine, University of Arkansas for Medical Sciences, 4301 W. Markham St, Slot 847, Little Rock, AR 72205, United States. Electronic address: kestephens@uams.edu.

Funding

Translational Regulation in Normal Erythropoiesis and Diamond Blackfan AnemiaP20GM121293 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Alan Tackett · 2017 to 2026
$27.6M
The Role of the Mitochondrion in the Metabolic Stress Response to Burn TraumaP20GM109096 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI SWINDLE, TAREN · 2016 to 2025
$20.7M
Training in Systems Pharmacology and Toxicology (T-SPaT)T32GM150536 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI William E Fantegrossi · 2023 to 2026
$708k
NIGMS NIH HHS P20 GM109096NIGMS NIH HHS P20 GM121293NIGMS NIH HHS T32 GM150536
6 · The paper itself

Abstract

Current evidence supports an association between chronic pain and the promotion of metabolic disorders, which can be further exacerbated by environmental factors. Early-life stress is an environmental risk factor that is well known to influence pain susceptibility. However, the maladaptive effects of early life stress on metabolism in the setting of chronic pain is unknown. In this study, we used the well-established limited bedding model of early life stress and subjected male and female adult offspring and controls to metabolic and behavioral profiling before and after peripheral nerve injury. We provide continuous, two-week, high-resolution profiling of animal food and water intake, physical movement, and energy expenditure data to study the effects of nerve injury-induced pain on metabolic outcomes in adult rats following exposure to early life stress. Additionally, we differentiate between dark and light cycles, which is crucial for understanding circadian rhythms in rodents. All offspring are assessed for baseline and post-injury mechanical sensitivity. We find that early life stress increases mechanical hypersensitivity following peripheral nerve injury in female offspring and reduces energy expenditures after peripheral nerve injury in male offspring. Our data provide valuable insights into metabolic and behavioral responses following nerve injury and contribute to understanding chronic pain development in both male and female rats. However, future studies are needed to understand the impact of our findings toward the promotion of metabolic disorders observed clinically. PERSPECTIVE: Mounting evidence supports associations between chronic pain and the promotion of metabolic disorders. We provide comprehensive metabolic assessments of the impact of ELS in the setting of nerve-injury induced pain to deepen our understanding of the mechanisms by which ELS influences pain sensitivity and metabolic outcomes after nerve injury.

Indexed as

Chronic PainEnergy MetabolismHyperalgesiaNeuralgiaPeripheral Nerve InjuriesStress, PsychologicalAnimalsDisease Models, AnimalFemaleMaleRatsRats, Sprague-DawleyChronic painEarly-life stressMetabolismNerve injurySomatosensory development

Identifiers

PMID41933815
PMCPMC13634588

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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.