Evidence map›Paper›PMID 12388616›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2002

Spinal neurons that possess the substance P receptor are required for the development of central sensitization.

Sergey G Khasabov, Scott D Rogers, Joseph R Ghilardi, Christopher M Peters, Patrick W Mantyh, Donald A Simone

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

74 citing papers in PubMed, 234 citations in OpenAlex.

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  11. Opioid-Induced Hyperalgesic Priming in Single Nociceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
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  16. Role of Nociceptor Toll-like Receptor 4 (TLR4) in Opioid-Induced Hyperalgesia and Hyperalgesic Priming.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  17. Article
  18. Presynaptic Inhibition of Primary Nociceptive Signals to Dorsal Horn Lamina I Neurons by Dopamine.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
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  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Sergey G KhasabovDepartment of Preventive Sciences, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Scott D Rogers
Joseph R Ghilardi
Christopher M Peters
Patrick W Mantyh
Donald A Simone
General Department of Preventive Medicine · VNUniversity of Minnesota · US

Funding

NEUROCHEMISTRY OF NOCICEPTIONR01DA011986 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MANTYH, PATRICK W · 1998 to 2002
$965k
NIDA NIH HHS DA11986
6 · The paper itself

Abstract

In previous studies, we have shown that loss of spinal neurons that possess the substance P receptor (SPR) attenuated pain and hyperalgesia produced by capsaicin, inflammation, and nerve injury. To determine the role of SPR-expressing neurons in modulating pain and hyperalgesia, responses of superficial and deep lumbar spinal dorsal horn neurons evoked by mechanical and heat stimuli and by capsaicin were made after ablation of SPR-expressing neurons using the selective cytotoxin conjugate substance P-saporin (SP-SAP). Morphological analysis and electrophysiological recordings were made after intrathecal infusion of vehicle, saporin alone, or SP-SAP. SP-SAP, but not vehicle or SAP alone, produced an approximately 62% decrease in SPR-expressing neurons in the dorsal horn. Loss of SPR-expressing neurons diminished the responses of remaining neurons to intraplantar injection of capsaicin. Peak responses to 10 microg of capsaicin were approximately 65% lower in animals pretreated with SP-SAP compared with controls. Additionally, sensitization to mechanical and heat stimuli that normally follows capsaicin was rarely observed. Importantly, responses to mechanical and heat stimuli in the absence of capsaicin were not altered after SP-SAP treatment. In addition, nociceptive neurons did not exhibit windup in the SP-SAP-treated group. These results demonstrate that SPR-expressing neurons located in the dorsal horn are a pivotal component of the spinal circuits involved in triggering central sensitization and hyperalgesia. It appears that this relatively small population of neurons can regulate the physiological properties of other nociceptive neurons and drive central sensitization.

Indexed as

N-Glycosyl HydrolasesAnimalsCapsaicinCytotoxinsHyperalgesiaImmunotoxinsInjections, SpinalMaleNeuronsNociceptorsPain MeasurementPhysical StimulationPlant ProteinsPosterior Horn CellsRatsRats, Sprague-DawleyCapsaicinCytotoxinsImmunotoxinsN-Glycosyl HydrolasesPlant ProteinsReceptors, Neurokinin-1Ribosome Inactivating Proteins, Type 1SaporinsSubstance Psubstance P-saporin

Identifiers

PMID12388616
PMCPMC6757691
OpenAlexW1970085850

What OpenQuestion holds

Textmetadata
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.