Evidence map›Paper›PMID 39725852›Full record

ArticleJournal of neurochemistry2025

Plasticity of Mouse Dorsal Root Ganglion Neurons by Innate Immune Activation Is Influenced by Electrophysiological Activity.

Timothy N Friedman, Shawn M Lamothe, Aislinn D Maguire, Thomas Hammond, Gustavo Tenorio, Brett J Hilton, Jason R Plemel, Harley T Kurata, Bradley J Kerr

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2025. 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. Shaping the Action Potential in Dorsal Root and Trigeminal Ganglia Neurons: Relevance to Pain Mechanisms.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Review
  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

9 authors.

Timothy N FriedmanNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Shawn M LamotheDepartment of Pharmacology, University of Alberta, Edmonton, Alberta, Canada.
Aislinn D MaguireNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Thomas HammondDepartment of Pharmacology, University of Alberta, Edmonton, Alberta, Canada.
Gustavo TenorioDepartment of Anesthesiology and Pain Medicine, University of Alberta, Edmonton, Alberta, Canada.
Brett J HiltonDepartment of Cellular and Physiological Sciences, International Collaboration on Repair Discoveries (ICORD), and Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, British Columbia, Canada.
Jason R PlemelNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
Harley T KurataDepartment of Pharmacology, University of Alberta, Edmonton, Alberta, Canada.
Bradley J KerrNeuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-0264-8316

Funding

Alberta MS NetworkCIHR FRN162434MS Canada EGID-MSSC-3761NSERCUniversity Hospital Fund (University of Alberta)
6 · The paper itself

Abstract

The complex relationship between inflammation, its effects on neuronal excitability and the ensuing plasticity of dorsal root ganglion (DRG) sensory neurons remains to be fully explored. In this study, we have employed a system of experiments assessing the impact of inflammatory conditioned media derived from activated immune cells on the excitability and activity of DRG neurons and how this relates to subsequent growth responses of these cells. We show here that an early phase of increased neuronal activity in response to inflammatory conditioned media is critical for the engagement of plastic processes and that neuronal excitability profiles are linked through time to the structural phenotype of individual neurons. Pharmacological blockade of neuronal activity was able to abolish the growth-promoting effects of inflammatory media. Our results suggest that targeting the activity of DRG neurons may provide a novel therapeutic avenue to manipulate their growth status and potential for plasticity in response to inflammation. Importantly, the same pharmacological blockade in vivo abolished pain responses in a mouse model of multiple sclerosis. While further studies are needed to fully elucidate the underlying mechanisms of the relationship between neural activity and growth status, a more complete understanding of this relationship may ultimately lead to the development of new treatments for neuropathic pain in disorders associated with heightened immune responses such as rheumatoid arthritis and multiple sclerosis.

Indexed as

Ganglia, SpinalImmunity, InnateMice, Inbred C57BLNeuronal PlasticityAction PotentialsAnimalsCells, CulturedCulture Media, ConditionedFemaleInflammationMaleMiceNeuronsSensory Receptor CellsCulture Media, ConditionedDRGelectrophysiologyinflammationKv7 channelsneurite extensionpainplasticityTNFα

Identifiers

PMID39725852
PMCPMC11671441

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.