Evidence map›Paper›PMID 16007234›Full record

ReviewCNS drug reviews2005

UFP-101, a peptide antagonist selective for the nociceptin/orphanin FQ receptor.

Girolamo Calo, Remo Guerrini, Anna Rizzi, Severo Salvadori, Melissa Burmeister, Daniel R Kapusta, David G Lambert, Domenico Regoli

Open access · bronzeAbstract readReview
In one paragraph

Review in CNS drug reviews, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Managing Parkinson's disease: moving ON with NOP.British journal of pharmacology · 2020
    Review
  6. NOP-Related Mechanisms in Substance Use Disorders.Handbook of experimental pharmacology · 2019
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Central N/OFQ-NOP Receptor System in Pain Modulation.Advances in pharmacology (San Diego, Calif.) · 2016
    Review
  12. Review
  13. Article
  14. Nociceptin system as a target in sepsis?Journal of anesthesia · 2014
    Review
  15. Stimulation of δ opioid receptor and blockade of nociceptin/orphanin FQ receptor synergistically attenuate parkinsonism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

8 authors at 4 institutions in 4 countries.

Girolamo CaloDepartment Experimental and Clinical Medicine, Section of Pharmacology and Neuroscience Centre, University of Ferrara, via Fossato di Mortara, 19, 44100 Ferrara, Italy. g.calo@unife.it
Remo Guerrini
Anna Rizzi
Severo Salvadori
Melissa Burmeister
Daniel R Kapusta
David G Lambert
Domenico Regoli
University of Ferrara · ITInstitut des Sciences Cognitives Marc Jeannerod · FRLouisiana State University Health Sciences Center New Orleans · USUniversity of Leicester · GB

Funding

Cardio-renal actions of novel nociceptin analoguesR01HL071212 · NHLBI · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2003 to 2008
$1.9M
NHLBI NIH HHS R01HL71212
6 · The paper itself

Abstract

Nociceptin/orphanin FQ modulates various biological functions at central and peripheral levels by selectively activating a G-protein coupled receptor named N/OFQ peptide (NOP) receptor. For extending our knowledge on the biological roles of the N/OFQ-NOP receptor system the identification of selective NOP ligands, especially antagonists, is mandatory. [Nphe1, Arg14, Lys15] N/OFQ-NH2 (UFP-101) is a novel NOP ligand that was designed by combining, in the same molecule, the [Nphe1] chemical modification which eliminates efficacy and the [Arg14, Lys15] substitution which increases ligand potency and duration of action in vivo. In the present article, we summarize the pharmacological features of UFP-101 as determined in a series of in vitro and in vivo assays. Moreover, some biological actions and possible therapeutic indications of NOP ligands are discussed on the basis of results obtained with UFP-101. Data obtained with this compound were compared with those generated using other NOP antagonists, especially J-113397 and [Nphe1]N/OFQ(1-13)-NH2, receptor or peptide knockout mice and other pharmacological tools useful for blocking N/OFQ - NOP receptor signaling. The analysis of the available data demonstrates that UFP-101 is a useful pharmacological tool for the investigation of the central and peripheral biological functions regulated by the N/OFQ-NOP receptor system and for defining the therapeutic potential of NOP receptor ligands.

Indexed as

Narcotic AntagonistsAnimalsCardiovascular SystemDose-Response Relationship, DrugHumansKidneyNervous SystemNociceptin ReceptorOpioid PeptidesPainReceptors, OpioidTime FactorsNarcotic AntagonistsNociceptin Receptor(Nphe(1),Arg(14),Lys(15))N-OFQ NH(2)Opioid PeptidesOPRL1 protein, humanReceptors, Opioid

Identifiers

PMID16007234
PMCPMC6741746
OpenAlexW1999413474

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.