Evidence map›Paper›PMID 18991730›Full record

ReviewCurrent topics in medicinal chemistry2008

The ORL-1 receptor system: are there opportunities for antagonists in pain therapy?

Beatriz Fioravanti, Todd W Vanderah

Abstract readReview
In one paragraph

Review in Current topics in medicinal chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. The placenta as a target of opioid drugs†.Biology of reproduction · 2022
    Review
  3. Review
  4. NOP-Related Mechanisms in Substance Use Disorders.Handbook of experimental pharmacology · 2019
    Article
  5. Review
  6. Pain and Poppies: The Good, the Bad, and the Ugly of Opioid Analgesics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Review
  7. Review
  8. Review
  9. Review
  10. Pharmacological pain management in chronic pancreatitis.World journal of gastroenterology · 2013
    Review
  11. Review
  12. 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

2 authors at 1 institution in 1 country.

Beatriz FioravantiDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ 85724, USA.
Todd W Vanderah
University of Arizona · US

Funding

Brain Stem Mechanisms of Opioid Induced PainK02DA018717 · NIDA · UNIVERSITY OF ARIZONA · PI VANDERAH, TODD W · 2005 to 2009
$477k
NIDA NIH HHS K02 DA018717
6 · The paper itself

Abstract

Following the cloning of the classical opioid receptors (mu, delta and kappa), the opioid receptor like-1 (ORL-1) was identified as a G-protein coupled receptor (GPCR) with 65% structure homology to the other members of the opioid family. Its endogenous ligand nociception/orphanin FQ (N/OFQ) was discovered shortly thereafter, becoming the subject of investigation in numerous studies. Since activation of the ORL-1 receptor by N/OFQ leads to G alpha(i)-coupling and signal transduction similar to that of opioid receptors, N/OFQ was thought to have a role in pain modulation, similar to that of the endogenous opioids. Surprisingly, studies characterizing N/OFQ's effects on pain transmission yielded conflicting results, attributing to N/OFQ both pronociceptive and antinociceptive actions, depending on doses and routes of administration as well as species and sex of the subjects. With the development of selective and potent ORL-1 antagonists, many scientists believed these contradicting actions would be elucidated. Here we review the recent literature reporting the use of novel ORL-1 antagonists, both peptide and non-peptide, in different models of pain and discuss their use as research tools or potential drug candidates.

Indexed as

Narcotic AntagonistsAnimalsHumansNociceptin ReceptorPainPain MeasurementPeptidesReceptors, OpioidStructure-Activity RelationshipNarcotic AntagonistsNociceptin ReceptorOPRL1 protein, humanPeptidesReceptors, Opioid

Identifiers

PMID18991730
PMCPMC13231405
OpenAlexW1997039364

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.