Evidence map›Paper›PMID 40233052›Full record

ArticlePloS one2025

Functional kinome profiling reveals brain protein kinase signaling pathways and gene networks altered by acute voluntary exercise in rats.

Chia-Ming Lee, Jennifer Nguyen, Brock Pope, Ali Sajid Imami, V William George Ryan, Smita Sahay, Victoria Mathis, Priyanka Pulvender, Hunter Michael Eby, Taylen Arvay and 4 more

Abstract read
In one paragraph

Article in PloS one, 2025. 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

14 authors.

Chia-Ming LeeDepartment of Physiology and Pharmacology, College of Osteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.ORCID 0000-0003-2346-9007
Jennifer NguyenDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Brock PopeDepartment of Physiology and Pharmacology, College of Osteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.
Ali Sajid ImamiDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
V William George RyanDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Smita SahayDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.ORCID 0009-0003-4377-8963
Victoria MathisDepartment of Physiology and Pharmacology, College of Osteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.
Priyanka PulvenderDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.ORCID 0009-0006-3306-5195
Hunter Michael EbyDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Taylen ArvayDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Khaled AlganemDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Lauren Wegman-PointsDepartment of Physiology and Pharmacology, College of Osteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.
Robert McCullunsmithDepartment of Neurosciences and Psychiatry, College of Medicine and Life Sciences, University of Toledo, Toledo, Ohio, United States of America.
Li-Lian YuanDepartment of Physiology and Pharmacology, College of Osteopathic Medicine, Des Moines University, Des Moines, Iowa, United States of America.ORCID 0000-0001-7787-576X

Funding

Translational assessment of brain bioenergetic function in schizophreniaR01MH121102 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI MARANO, CHRISTOPHER, MCCULLUMSMITH, ROBERT E · 2020 to 2024
$3.7M
Cell-specific analysis of sub-kinomes in schizophreniaR01MH107487 · NIMH · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI MCCULLUMSMITH, ROBERT E, MELLER, JAREK · 2016 to 2020
$1.9M
Training in Molecular and translational Cell DynamicsT32GM144873 · NIGMS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI AVIDOR-REISS, TOMER, DWORKIN, LANCE DOUGLAS · 2022 to 2024
$1.3M
American Heart Association-American Stroke Association 24TPA1298609NIGMS NIH HHS T32 GM144873NIMH NIH HHS R01 MH107487NIMH NIH HHS R01 MH121102
6 · The paper itself

Abstract

Regular exercise confers numerous physical and mental health benefits, yet individual variability in exercise participation and outcomes is still poorly understood. Uncovering the neurobiological mechanisms governing exercise behavior is essential for promoting physical activity and developing targeted interventions for related disorders. While genetic studies have provided insights, they often cannot account for protein-level alterations, such as changes in kinase activity. Here, we employ protein kinase activity profiling to delineate brain protein kinase activity and signaling networks modulated by acute voluntary exercise in rats. Focusing on the dorsal striatum, which governs voluntary exercise, as well as the hippocampus, which is susceptible to modulation by physical activity, we aim to understand the molecular basis of exercise behavior. Utilizing high throughput kinome array profiling and advanced pathway analyses, we identified protein kinase signaling pathways implicated in regulating voluntary exercise. Pathway analysis using Gene Ontology (GO) revealed significant alterations in 155 GO terms in the dorsal striatum and 206 GO terms in the hippocampus. Changes in kinase activity were observed in the striatum and hippocampus between the exercise (voluntary wheel running, VWR) and sedentary control rats. In both regions, global serine-threonine kinase (STK) activity was decreased, while global phospho-tyrosine kinase (PTK) activity was increased in VWR rats compared to control rats. We also identified specific kinases altered in VWR rats, including the IKappaB Kinase (IKK) and protein kinase delta (PKD) families. C-terminal src Kinase (CSK), epidermal growth factor (EGFR), and vascular endothelial growth factor receptor (VEGFR) tyrosine kinase were also enriched. These findings suggest regional heterogeneity of kinase activity following voluntary exercise, emphasizing potential molecular mechanisms underlying exercise behavior. This exploratory study lays the groundwork for future investigations into the causality of variations in exercise outcomes among individuals and different sexes, as well as the development of targeted interventions to promote physical activity and combat associated chronic diseases.

Indexed as

BrainGene Regulatory NetworksPhysical Conditioning, AnimalProtein KinasesSignal TransductionAnimalsCorpus StriatumHippocampusMaleRatsRats, Sprague-DawleyProtein Kinases

Identifiers

PMID40233052
PMCPMC11999169

What Socratic holds

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LicenceCC BY
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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 Socratic graph.