Evidence map›Paper›PMID 24184978›Full record

ArticleNeuroscience2014

Neonatal tissue injury reduces the intrinsic excitability of adult mouse superficial dorsal horn neurons.

J Li, M L Baccei

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-weighted citation impact, top 17% 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, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Editorial: Insight in pediatric pain - 2023.Frontiers in pain research (Lausanne, Switzerland) · 2024
    Article
  6. CaInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Article
  9. Neonatal Injury Evokes Persistent Deficits in Dynorphin Inhibitory Circuits within the Adult Mouse Superficial Dorsal Horn.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  10. The development of pain circuits and unique effects of neonatal injury.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  11. Neonatal Injury Alters Sensory Input and Synaptic Plasticity in GABAergic Interneurons of the Adult Mouse Dorsal Horn.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Inward-rectifying KNeuroscience · 2016
    Article
  18. Review
  19. [Patterns of action potential firing in cortical neurons of neonatal mice and their electrophysiological property].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2016
    Article
  20. Neonatal Tissue Damage Promotes Spike Timing-Dependent Synaptic Long-Term Potentiation in Adult Spinal Projection Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    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

2 authors at 1 institution in 1 country.

J LiPain Research Center, Department of Anesthesiology, University of Cincinnati Medical Center, 231 Albert Sabin Way, Cincinnati, OH 45267, USA. Electronic address: li2je@uc.edu.
M L BacceiPain Research Center, Department of Anesthesiology, University of Cincinnati Medical Center, 231 Albert Sabin Way, Cincinnati, OH 45267, USA. Electronic address: mark.baccei@uc.edu.
University of Cincinnati · US

Funding

Developmental Regulation of Intrinsic Excitability in Spinal Pain NetworksR01NS072202 · NINDS · UNIVERSITY OF CINCINNATI · PI BACCEI, MARK L · 2010 to 2020
$3.4M
NINDS NIH HHS NS072202NINDS NIH HHS R01 NS072202
6 · The paper itself

Abstract

Tissue damage during the neonatal period evokes long-lasting changes in nociceptive processing within the adult spinal cord which contribute to persistent alterations in pain sensitivity. However, it remains unclear if the observed modifications in neuronal activity within the mature superficial dorsal horn (SDH) following early injury reflect shifts in the intrinsic membrane properties of these cells. Therefore, the present study was undertaken to identify the effects of neonatal surgical injury on the intrinsic excitability of both GABAergic and presumed glutamatergic neurons within lamina II of the adult SDH using in vitro patch clamp recordings from spinal cord slices prepared from glutamic acid decarboxylase-green fluorescent protein (Gad-GFP) mice. The results demonstrate that hindpaw surgical incision at postnatal day (P) 3 altered the passive membrane properties of both Gad-GFP and adjacent, non-GFP neurons in the mature SDH, as evidenced by decreased membrane resistance and more negative resting potentials in comparison to naïve littermate controls. This was accompanied by a reduction in the prevalence of spontaneous activity within the GABAergic population. Both Gad-GFP and non-GFP neurons displayed a significant elevation in rheobase and decreased instantaneous firing frequency after incision, suggesting that early tissue damage lowers the intrinsic membrane excitability of adult SDH neurons. Isolation of inward-rectifying K(+) (K(ir)) currents revealed that neonatal incision significantly increased K(ir) conductance near physiological membrane potentials in GABAergic, but not glutamatergic, lamina II neurons. Overall, these findings suggest that neonatal tissue injury causes a long-term dampening of intrinsic firing across the general population of lamina II interneurons, but the underlying ionic mechanisms may be cell-type specific.

Indexed as

Action PotentialsAnalysis of VarianceAnimalsAnimals, NewbornBiophysicsElectric StimulationFemaleGanglia, SpinalGlutamate DecarboxylaseGreen Fluorescent ProteinsIn Vitro TechniquesMiceMice, TransgenicNeuronsPatch-Clamp TechniquesPotassium ChannelsGlutamate Decarboxylaseglutamate decarboxylase 1Green Fluorescent ProteinsPotassium ChannelsaCSFaction potentialanalysis of varianceANOVAAPartificial cerebrospinal fluidC(m)developmenteGFPenhanced GFPE(rev)Gad-GFPglutamic acid decarboxylase-green fluorescent proteinHEPESIFincisioninstantaneous firing frequencyinward-rectifying K(+)K(ir)lamina IImembrane capacitancemembrane potentialmembrane resistanceN-(2-hydroxyethyl)piperazine-N′-2-ethanesulfonic acidpatch clampresting membrane potentialreversal potentialR(m)SDHspinal cordsuperficial dorsal hornV(m)V(rest)

Identifiers

PMID24184978
PMCPMC3894930
OpenAlexW2011864738

What OpenQuestion holds

Textmetadata
LicenceTDM
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.