Evidence map›Paper›PMID 41248749›Full record

ReviewBiological psychiatry2026

Functional Plasticity of Orexin/Hypocretin Neurons Balances Stress States.

Jazmine D W Yaeger, Morgan H James, Cliff H Summers

Abstract readReview
In one paragraph

Review in Biological psychiatry, 2026. 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. Orexinergic responses to environmental stressors in the zebrafish gut.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2026
    Article
  2. 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

3 authors.

Jazmine D W YaegerCellular Therapies and Stem Cell Biology Group, Sanford Research, Sioux Falls, South Dakota.
Morgan H JamesBrain and Mind Centre, University of Sydney, Sydney, New South Wales, Australia; School of Psychology, Faculty of Science, University of Sydney, Sydney, New South Wales, Australia; Department of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, Piscataway, New Jersey; Rutgers Addiction Research Center, Brain Health Institute, Rutgers Health, Piscataway, New Jersey.
Cliff H SummersDepartment of Biology, University of South Dakota, Vermillion, South Dakota; Neuroscience Group, Division of Biomedical and Translational Sciences, Sanford School of Medicine, University of South Dakota, Vermillion, South Dakota; Veterans Affairs Research Service, Sioux Falls Veteran Affairs Health Care System, Sioux Falls, South Dakota. Electronic address: cliff@usd.edu.

Funding

Availability, accessibility, and structure of opioid use disorder treatment and maternal and child health outcomesR01DA045675 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JARLENSKI, MARIAN PATRICIA, KRANS, ELIZABETH E · 2018 to 2022
$3.4M
Orexin (hypocretin) signaling in ventral tegmental area as a common mediator of sleep disturbances and drug demand in cocaine abstinenceR01DA061303 · NIDA · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Gary S. Aston-Jones, Morgan H. James · 2024 to 2026
$1.1M
Sex Differences in the Neurobiological Significance of Orexin Stress SignalingR15MH125306 · NIMH · UNIVERSITY OF SOUTH DAKOTA · PI SUMMERS, CLIFF H · 2021 to 2021
$427k
Amygdalar Orexin Modulation of Affective DisordersR15MH104485 · NIMH · UNIVERSITY OF SOUTH DAKOTA · PI SUMMERS, CLIFF H · 2015 to 2015
$426k
NIDA NIH HHS R01 DA045675NIDA NIH HHS R01 DA061303NIMH NIH HHS R15 MH104485NIMH NIH HHS R15 MH125306
6 · The paper itself

Abstract

Orexin/hypocretin (Orx) peptides critically contribute to stress and arousal circuits' flexibility and equilibrium. New discoveries highlight plasticity of orexin neurons themselves, as well as plasticity-inducing properties of orexin peptides within projection circuits, as an integral part of this function. Specifically, orexin peptide release in response to stress alters the microcircuitry and gene expression profile of downstream stress regions. Here, we propose that orexin-mediated plasticity within stress circuitry is constructed across a lifetime in response to a myriad of variable challenges, ultimately enhancing neural flexibility and future adaptive behavioral responses. This provides a framework through which exposure to unusually salient stressors, either acutely or over extended periods, can result in altered engagement of stress circuitry and maladaptive affective behavioral outcomes (as in general anxiety disorder and posttraumatic stress disorder). Furthermore, we posit that the diversity of plastic orexin functions is regulated, at least in part, by unique signaling roles for Orx 1 and 2 receptors in distinct brain regions. By extension, therapeutics with selective actions at these receptors may offer viable treatments designed to override pathological rewiring of stress circuits and restore adaptive stress responsivity.

Indexed as

BrainNeuronal PlasticityNeuronsOrexinsStress, PsychologicalAnimalsHumansIntracellular Signaling Peptides and ProteinsNeuropeptidesOrexin ReceptorsIntracellular Signaling Peptides and ProteinsNeuropeptidesOrexin ReceptorsOrexinsHomeostasisIGF(1)NeurocircuitriesNeuroplasticityPsychopathologyReserve

Identifiers

PMID41248749
PMCPMC12768429

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.