Evidence map›Paper›PMID 25019623›Full record

ArticlePloS one2014

Spinal cord transection-induced allodynia in rats--behavioral, physiopathological and pharmacological characterization.

Saïd M'Dahoma, Sylvie Bourgoin, Valérie Kayser, Sandrine Barthélémy, Caroline Chevarin, Farah Chali, Didier Orsal, Michel Hamon

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
2.6field-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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Modelling at-level allodynia after mid-thoracic contusion in the rat.European journal of pain (London, England) · 2021
    Article
  11. Article
  12. Effects ofEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Neuropathic Pain After Spinal Cord Injury: Challenges and Research Perspectives.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. A Combination ofFrontiers in aging neuroscience · 2017
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Saïd M'DahomaCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Sylvie BourgoinCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Valérie KayserCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Sandrine BarthélémyCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Caroline ChevarinCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Farah ChaliLaboratoire de Neurobiologie des Signaux Intercellulaires, Centre National de la Recherche Scientifique, CNRS UMR 7101, Université Pierre et Marie Curie, Paris, France.
Didier OrsalLaboratoire de Neurobiologie des Signaux Intercellulaires, Centre National de la Recherche Scientifique, CNRS UMR 7101, Université Pierre et Marie Curie, Paris, France.
Michel HamonCentre de Psychiatrie et Neurosciences, Institut National de la Santé et de la Recherche Médicale, INSERM U894, Université Paris Descartes, Paris, France; Neuropsychopharmacologie, Faculté de Médecine Pierre et Marie Curie, site Pitié-Salpêtrière, Paris, France.
Centre National de la Recherche Scientifique · FRInserm · FRSorbonne Université · FRInstitut de Psychiatrie et Neurosciences de Paris · FRUniversité Paris Cité · FR

Funding

Wellcome Trust
6 · The paper itself

Abstract

In humans, spinal cord lesions induce not only major motor and neurovegetative deficits but also severe neuropathic pain which is mostly resistant to classical analgesics. Better treatments can be expected from precise characterization of underlying physiopathological mechanisms. This led us to thoroughly investigate (i) mechanical and thermal sensory alterations, (ii) responses to acute treatments with drugs having patent or potential anti-allodynic properties and (iii) the spinal/ganglion expression of transcripts encoding markers of neuronal injury, microglia and astrocyte activation in rats that underwent complete spinal cord transection (SCT). SCT was performed at thoracic T8-T9 level under deep isoflurane anaesthesia, and SCT rats were examined for up to two months post surgery. SCT induced a marked hyper-reflexia at hindpaws and strong mechanical and cold allodynia in a limited (6 cm2) cutaneous territory just rostral to the lesion site. At this level, pressure threshold value to trigger nocifensive reactions to locally applied von Frey filaments was 100-fold lower in SCT- versus sham-operated rats. A marked up-regulation of mRNAs encoding ATF3 (neuronal injury) and glial activation markers (OX-42, GFAP, P2×4, P2×7, TLR4) was observed in spinal cord and/or dorsal root ganglia at T6-T11 levels from day 2 up to day 60 post surgery. Transcripts encoding the proinflammatory cytokines IL-1β, IL-6 and TNF-α were also markedly but differentially up-regulated at T6-T11 levels in SCT rats. Acute treatment with ketamine (50 mg/kg i.p.), morphine (3-10 mg/kg s.c.) and tapentadol (10-20 mg/kg i.p.) significantly increased pressure threshold to trigger nocifensive reaction in the von Frey filaments test, whereas amitriptyline, pregabalin, gabapentin and clonazepam were ineffective. Because all SCT rats developed long lasting, reproducible and stable allodynia, which could be alleviated by drugs effective in humans, thoracic cord transection might be a reliable model for testing innovative therapies aimed at reducing spinal cord lesion-induced central neuropathic pain.

Indexed as

Activating Transcription Factor 3Analysis of VarianceAnimalsCytokinesGanglia, SpinalHot TemperatureHyperalgesiaKetamineMaleMorphineNerve Tissue ProteinsPain MeasurementPhenolsRatsRats, Sprague-DawleyReal-Time Polymerase Chain ReactionActivating Transcription Factor 3Atf3 protein, ratCytokinesKetamineMorphineNerve Tissue ProteinsPhenolsTapentadol

Identifiers

PMID25019623
PMCPMC4096923
OpenAlexW2159302234

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.