Evidence map›Paper›PMID 29582417›Full record

ArticleBritish journal of pharmacology2018

Analysis of the distribution of spinal NOP receptors in a chronic pain model using NOP-eGFP knock-in mice.

Akihiko Ozawa, Gloria Brunori, Andrea Cippitelli, Nicholas Toll, Jennifer Schoch, Brigitte L Kieffer, Lawrence Toll

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. The Downregulation of Opioid Receptors and Neuropathic Pain.International journal of molecular sciences · 2023
    Review
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  14. Review
  15. Pain And Opioid Systems, Implications In The Opioid Epidemic.Current opinion in behavioral sciences · 2019
    Article
  16. Article
  17. 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

7 authors at 2 institutions in 2 countries.

Akihiko OzawaTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.ORCID 0000-0002-4471-7076
Gloria BrunoriTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.
Andrea CippitelliTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.
Nicholas TollTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.
Jennifer SchochTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.
Brigitte L KiefferDouglas Research Center, Department of Psychiatry, Faculty of Medicine, McGill University, Montreal, QC, H4H 1R3, Canada.
Lawrence TollTorrey Pines Institute for Molecular Studies, Port St. Lucie, FL, 34987, USA.
Torrey Pines Institute For Molecular Studies · USDouglas Mental Health University Institute · CA

Funding

MIXED NOP/MU COMPOUNDS AND THE INVOLVEMENT OF THEIR RECEPTORS IN ANALGESIAR01DA023281 · NIDA · TORREY PINES INST FOR MOLECULAR STUDIES · PI TOLL, LAWRENCE R · 2007 to 2021
$6.4M
NIDA NIH HHS R01 DA023281
6 · The paper itself

Abstract

background and purposeThe nociceptin/orphanin FQ opioid peptide (NOP) receptor system plays a significant role in the regulation of pain. This system functions differently in the spinal cord and brain. The mechanism by which the NOP receptor agonists regulate pain transmission in these regions is not clearly understood. Here, we investigate the peripheral and spinal NOP receptor distribution and antinociceptive effects of intrathecal nociceptin/orphanin FQ (N/OFQ) in chronic neuropathic pain. EXPERIMENTAL APPROACH: We used immunohistochemistry to determine changes in NOP receptor distribution triggered by spinal nerve ligation (SNL) using NOP-eGFP knock-in mice. Antinociceptive effects of intrathecal N/OFQ on SNL-mediated allodynia and heat/cold hyperalgesia were assessed in wild-type mice. KEY

resultsNOP-eGFP immunoreactivity was decreased by SNL in the spinal laminae I and II outer, regions that mediate noxious heat stimuli. In contrast, immunoreactivity of NOP-eGFP was unchanged in the ventral border of lamina II inner, which is an important region for the development of allodynia. NOP-eGFP expression was also decreased in a large number of primary afferents in the L4 dorsal root ganglion (DRG) of SNL mice. However, SNL mice showed increased sensitivity, compared to sham animals to the effects of i.t administered N/OFQ with respect to mechanical as well as thermal stimuli. CONCLUSIONS AND IMPLICATIONS: Our findings suggest that the spinal NOP receptor system attenuates injury-induced hyperalgesia by direct inhibition of the projection neurons in the spinal cord that send nociceptive signals to the brain and not by inhibiting presynaptic terminals of DRG neurons in the superficial lamina.

Indexed as

Disease Models, AnimalAnalgesics, OpioidAnimalsChronic PainFemaleGene Knock-In TechniquesGreen Fluorescent ProteinsInjections, SpinalMaleMiceMice, Inbred C57BLNociceptin ReceptorOpioid PeptidesReceptors, OpioidSpinal CordAnalgesics, Opioidenhanced green fluorescent proteinGreen Fluorescent ProteinsNociceptin ReceptorOpioid PeptidesOprl1 protein, mouseReceptors, Opioid

Identifiers

PMID29582417
PMCPMC6003644
OpenAlexW2795358691

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.