Evidence map›Paper›PMID 25986444›Full record

ArticleJournal of neuroinflammation2015

Evidence for a distinct neuro-immune signature in rats that develop behavioural disability after nerve injury.

Paul J Austin, Annika M Berglund, Sherman Siu, Nathan T Fiore, Michelle B Gerke-Duncan, Suzanne L Ollerenshaw, Sarah-Jane Leigh, Priya A Kunjan, James W M Kang, Kevin A Keay

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 10% of its field
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

33 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Probiotic and high-fat diet: effects on pain assessment, body composition, and cytokines in male and female adolescent and adult rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2024
    Article
  6. Minocycline Abrogates Individual Differences in Nerve Injury-Evoked Affective Disturbances in Male Rats and Prevents Associated Supraspinal Neuroinflammation.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Myricetin prevents sleep deprivation-induced cognitive impairment and neuroinflammation in rat brainThe Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Stem Cell Therapy for Modulating Neuroinflammation in Neuropathic Pain.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Review
  18. Chemokine Signaling in Chemotherapy-Induced Neuropathic Pain.International journal of molecular sciences · 2019
    Review
  19. Article
  20. 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

10 authors at 1 institution in 1 country.

Paul J AustinDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. paustin@anatomy.usyd.edu.au.
Annika M BerglundDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. aber4607@uni.sydney.edu.au.
Sherman SiuDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. ssiu5308@uni.sydney.edu.au.
Nathan T FioreDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. nfio4364@uni.sydney.edu.au.
Michelle B Gerke-DuncanDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. mbg@anatomy.usyd.edu.au.
Suzanne L OllerenshawDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. slo@anatomy.usyd.edu.au.
Sarah-Jane LeighDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. slei3376@uni.sydney.edu.au.
Priya A KunjanDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. priya.kunjan@gmail.com.
James W M KangDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. jkan5634@uni.sydney.edu.au.
Kevin A KeayDiscipline of Anatomy and Histology, School of Medical Sciences, The University of Sydney, Room E511, Anderson Stuart Building F13, Sydney, NSW, 2006, Australia. keay@anatomy.usyd.edu.au.
University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic neuropathic pain is a neuro-immune disorder, characterised by allodynia, hyperalgesia and spontaneous pain, as well as debilitating affective-motivational disturbances (e.g., reduced social interactions, sleep-wake cycle disruption, anhedonia, and depression). The role of the immune system in altered sensation following nerve injury is well documented. However, its role in the development of affective-motivational disturbances remains largely unknown. Here, we aimed to characterise changes in the immune response at peripheral and spinal sites in a rat model of neuropathic pain and disability.

methodsSixty-two rats underwent sciatic nerve chronic constriction injury (CCI) and were characterised as either Pain and disability, Pain and transient disability or Pain alone on the basis of sensory threshold testing and changes in post-CCI dominance behaviour in resident-intruder interactions. Nerve ultrastructure was assessed and the number of T lymphocytes and macrophages were quantified at the site of injury on day six post-CCI. ATF3 expression was quantified in the dorsal root ganglia (DRG). Using a multiplex assay, eight cytokines were quantified in the sciatic nerve, DRG and spinal cord.

resultsAll CCI rats displayed equal levels of mechanical allodynia, structural nerve damage, and reorganisation. All CCI rats had significant infiltration of macrophages and T lymphocytes to both the injury site and the DRG. Pain and disability rats had significantly greater numbers of T lymphocytes. CCI increased IL-6 and MCP-1 in the sciatic nerve. Examination of disability subgroups revealed increases in IL-6 and MCP-1 were restricted to Pain and disability rats. Conversely, CCI led to a decrease in IL-17, which was restricted to Pain and transient disability and Pain alone rats. CCI significantly increased IL-6 and MCP-1 in the DRG, with IL-6 restricted to Pain and disability rats. CCI rats had increased IL-1β, IL-6 and MCP-1 in the spinal cord. Amongst subgroups, only Pain and disability rats had increased IL-1β.

conclusionsThis study has defined individual differences in the immune response at peripheral and spinal sites following CCI in rats. These changes correlated with the degree of disability. Our data suggest that individual immune signatures play a significant role in the different behavioural trajectories following nerve injury, and in some cases may lead to persistent affective-motivational disturbances.

Indexed as

AnhedoniaAnimalsBehavior, AnimalChemokine CCL2DepressionDisease Models, AnimalInterleukin-6MacrophagesMaleNeuralgiaNeuroimmunomodulationRatsRats, Sprague-DawleySciatic NerveSensory ThresholdsSleep Disorders, Circadian RhythmCcl2 protein, ratChemokine CCL2Interleukin-6

Identifiers

PMID25986444
PMCPMC4506439
OpenAlexW1492728201

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.