Evidence map›Paper›PMID 31533959›Full record

ArticleeNeuro

Functional Reorganization of Local Circuit Connectivity in Superficial Spinal Dorsal Horn with Neuropathic Pain States.

Nian Gong, Garo Hagopian, Todd C Holmes, Z David Luo, Xiangmin Xu

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Spinal neuropeptide Y Y1 receptor-expressing neurons are a pharmacotherapeutic target for the alleviation of neuropathic pain.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Review
  6. Excitatory and Inhibitory Neurons of the Spinal Cord Superficial Dorsal Horn Diverge in Their Somatosensory Responses and PlasticityThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  7. Review
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

5 authors at 1 institution in 1 country.

Nian GongDepartment of Anesthesiology & Perioperative Care, School of Medicine, University of California, Irvine, Orange, California 92868.
Garo HagopianDepartment of Anesthesiology & Perioperative Care, School of Medicine, University of California, Irvine, Orange, California 92868.
Todd C HolmesDepartment of Physiology & Biophysics, School of Medicine, University of California, Irvine, Irvine, California 92697.ORCID 0000-0001-8152-8832
Z David LuoDepartment of Anesthesiology & Perioperative Care, School of Medicine, University of California, Irvine, Orange, California 92868 zluo@uci.edu xiangmin.xu@uci.edu.ORCID 0000-0001-6811-9380
Xiangmin XuDepartment of Anatomy & Neurobiology, School of Medicine, University of California, Irvine, Irvine, California 92697 zluo@uci.edu xiangmin.xu@uci.edu.ORCID 0000-0002-5828-1533
University of California, Irvine · US

Funding

UV to blue neuronal phototransduction mechanismsR35GM127102 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Todd C Holmes · 2018 to 2026
$4.4M
A novel pathway mediating the development of chronic orofacial neuropathic painR01DE021847 · NIDCR · UNIVERSITY OF CALIFORNIA-IRVINE · PI LUO, ZHIGANG DAVID, STEWARD, OSWALD · 2011 to 2015
$3.6M
Subiculm circuits for cortical feedback regulation of spatial mapping and learningR01NS104897 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI NITZ, DOUGLAS ARTHUR, XU, XIANGMIN · 2018 to 2022
$2.6M
Hippocampal inhibitory neuronal circuit organizationR01NS078434 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI XU, XIANGMIN · 2012 to 2016
$1.6M
Mechanism of Calcium Channel Cava2d1 Protein Mediated Neuropathic PainR01NS064341 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LUO, ZHIGANG DAVID · 2010 to 2013
$1.2M
Defining Target Contribution To Orofacial Pain By Antisense OligonucleotidesR21DE019298 · NIDCR · UNIVERSITY OF CALIFORNIA-IRVINE · PI LUO, ZHIGANG DAVID · 2008 to 2009
$661k
NIDCR NIH HHS R01 DE021847NIDCR NIH HHS R21 DE019298NIGMS NIH HHS R35 GM127102NINDS NIH HHS R01 NS064341NINDS NIH HHS R01 NS078434NINDS NIH HHS R01 NS104897
6 · The paper itself

Abstract

The spinal dorsal horn is the first relay structure coding for pain transmission and modulation. Previous anatomical and electrophysiological studies have examined spinal dorsal horn circuit connections and network activity. Further work is required to understand spinal cord sensory information processing that underlies pathological neuropathic pain states. Our previous studies suggest that peripheral nerve injury enhances presynaptic excitatory input onto spinal superficial dorsal horn neurons, which in turn contributes to pathologic nociception. The potential changes in local postsynaptic circuits in the dorsal horn that lead to pathologically heightened behavioral responses to pain remain largely unexplored. We combined whole-cell electrophysiological recordings with laser-scanning photostimulation to test whether peripheral nerve injury in the spinal nerve ligation (SNL) mouse model of neuropathic pain leads to alterations in the functional connectivity of spinal cord circuits including lamina II excitatory interneurons. Here we show that SNL enhances excitation and decreases inhibition to lamina II excitatory interneurons along with their increased glutamate-evoked excitability. The enhanced excitatory postsynaptic input and connectivity evoked by SNL eventually return to normal levels concurrently with the resolution of the neuropathic pain states. The physiological pattern highly correlates with mouse pain behaviors following SNL, supporting a neurophysiological mechanism of central sensitization and neuropathic pain that is functionally localized to the spinal dorsal horn. Together, these data support that SNL induces functional changes in synaptic input and connectivity to lamina II excitatory interneurons that code for pain perception, and thus provide new insights into the mechanism and locus of pain hypersensitivity.

Indexed as

AnimalsExcitatory Postsynaptic PotentialsInhibitory Postsynaptic PotentialsMaleMiceMice, TransgenicNerve NetNeuralgiaNeuronal PlasticityOrgan Culture TechniquesPain MeasurementSpinal Cord Dorsal Hornelectrophysiologyexcitatoryinhibitoryphotostimulationsynaptic connections

Identifiers

PMID31533959
PMCPMC6787342
OpenAlexW2974790799

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.