Evidence map›Paper›PMID 19279568›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2009

Behavioral effects of a synthetic agonist selective for nociceptin/orphanin FQ peptide receptors in monkeys.

Mei-Chuan Ko, James H Woods, William E Fantegrossi, Chad M Galuska, Jürgen Wichmann, Eric P Prinssen

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

58 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. NOP agonist AT-403 promoted sleep in lactic acid-induced acute pain model.Frontiers in pain research (Lausanne, Switzerland) · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Potential therapeutic targets for the treatment of opioid abuse and pain.Advances in pharmacology (San Diego, Calif.) · 2022
    Review
  8. Article
  9. Review
  10. Opioid Analgesia and Opioid-Induced Adverse Effects: A Review.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  11. Article
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  15. Article
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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 4 institutions in 2 countries.

Mei-Chuan KoDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109-5632, USA. mko@umich.edu
James H Woods
William E Fantegrossi
Chad M Galuska
Jürgen Wichmann
Eric P Prinssen
Roche (Switzerland) · CHUniversity of Michigan–Ann Arbor · USCollege of Charleston · USUniversity of Arkansas for Medical Sciences · US

Funding

Narcotic Drug and Opioid Peptide Basic Research projectP01DA000254 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOODS, JAMES H · 2003 to 2006
$5.0M
Behavioral Economic Analysis of Polydrug AbuseR01DA015449 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WINGER, GAIL D · 2003 to 2010
$3.5M
NIDA NIH HHS DA-015449NIDA NIH HHS P01 DA000254NIDA NIH HHS R01 DA015449
6 · The paper itself

Abstract

Behavioral effects of a nonpeptidic NOP (nociceptin/orphanin FQ Peptide) receptor agonist, Ro 64-6198, have not been studied in primate species. The aim of the study was to verify the receptor mechanism underlying the behavioral effects of Ro 64-6198 and to systematically compare behavioral effects of Ro 64-6198 with those of a mu-opioid receptor agonist, alfentanil, in monkeys. Both Ro 64-6198 (0.001-0.06 mg/kg, s.c.) and alfentanil (0.001-0.06 mg/kg, s.c.) produced antinociception against an acute noxious stimulus (50 degrees C water) and capsaicin-induced allodynia. An NOP receptor antagonist, J-113397 (0.01-0.1 mg/kg, s.c.), dose-dependently produced rightward shifts of the dose-response curve of Ro 64-6198-induced antinociception. The apparent pA(2) value of J-113397 was 8.0. Antagonist studies using J-113397 and naltrexone revealed that Ro 64-6198 produced NOP receptor-mediated antinociception independent of mu-opioid receptors. In addition, alfentanil dose-dependently produced respiratory depression and itch/scratching responses, but antinociceptive doses of Ro 64-6198 did not produce such effects. More important, Ro 64-6198 did not produce reinforcing effects comparable with those of alfentanil, cocaine, or methohexital under self-administration procedures in monkeys. These results provide the first functional evidence that the activation of NOP receptors produces antinociception without reinforcing effects in primates. Non-peptidic NOP receptor agonists may have therapeutic value as novel analgesics without abuse liability in humans.

Indexed as

AlfentanilAnalgesics, OpioidAnimalsBehavior, AnimalBenzimidazolesCapsaicinCentral Nervous System AgentsDose-Response Relationship, DrugFemaleHot TemperatureImidazolesMacaca mulattaMaleNaltrexoneNarcotic AntagonistsNociceptin ReceptorAlfentanilAnalgesics, OpioidBenzimidazolesCapsaicinCentral Nervous System AgentsImidazolesJ 113397NaltrexoneNarcotic AntagonistsNociceptin ReceptorPiperidinesReceptors, OpioidReceptors, Opioid, muRo 64-6198Spiro Compounds

Identifiers

PMID19279568
PMCPMC2804925
OpenAlexW2025043134

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.