Evidence map›Paper›PMID 19711054›Full record

ArticlePsychopharmacology2009

Chronic treatment with the selective NOP receptor antagonist [Nphe 1, Arg 14, Lys 15]N/OFQ-NH 2 (UFP-101) reverses the behavioural and biochemical effects of unpredictable chronic mild stress in rats.

Giovanni Vitale, Valentina Ruggieri, Monica Filaferro, Claudio Frigeri, Silvia Alboni, Fabio Tascedda, Nicoletta Brunello, Remo Guerrini, Carlo Cifani, Maurizio Massi

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.1field-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

35 citing papers in PubMed, 74 citations in OpenAlex.

  1. A Selective Nociceptin Receptor Antagonist to Treat Depression: Evidence from Preclinical and Clinical Studies.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. The opioid system in depression.Neuroscience and biobehavioral reviews · 2022
    Review
  8. Article
  9. Review
  10. Adolescent neuroimmune function and its interaction with alcohol.International review of neurobiology · 2022
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Role of nociceptin/orphanin FQ and nociceptin opioid peptide receptor in depression and antidepressant effects of nociceptin opioid peptide receptor antagonists.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2019
    Review
  16. Review
  17. Article
  18. Article
  19. Brain mechanisms mediating effects of stress on reward sensitivity.Current opinion in behavioral sciences · 2018
    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

10 authors at 3 institutions in 1 country.

Giovanni VitaleDepartment of Biomedical Sciences, Section of Pharmacology, University of Modena and Reggio Emilia, 41100, Modena, Italy. giovanni.vitale@unimore.it
Valentina Ruggieri
Monica Filaferro
Claudio Frigeri
Silvia Alboni
Fabio Tascedda
Nicoletta Brunello
Remo Guerrini
Carlo Cifani
Maurizio Massi
University of Modena and Reggio Emilia · ITUniversità di Camerino · ITUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe present study was designed to assess the antidepressant effects of UFP-101, a selective nociceptin/orphanin FQ peptide (NOP) receptor antagonist, in a validated animal model of depression: the chronic mild stress (CMS). MATERIALS AND METHODS AND

resultsUFP-101 (5, 10 and 20 nmol/rat; i.c.v., once a day for 21 days) dose- and time-dependently reinstated sucrose consumption in stressed animals without affecting the same parameter in non-stressed ones. In the forced swimming test, UFP-101 reduced immobility of stressed rats from day 8 of treatment. After a 3-week treatment, rats were killed for biochemical evaluations. UFP-101 abolished increase in serum corticosterone induced by CMS and reverted changes in central 5-HT/5-HIAA ratio. The behavioural and biochemical effects of UFP-101 mimicked those of imipramine, the reference antidepressant drug, administered at the dose of 15 mg/kg (i.p.). Co-administration of nociceptin/orphanin FQ (5 nmol/rat, from day 12 to 21) prevented the effects of UFP-101. Brain-derived neurotrophic factor mRNA and protein in hippocampus were not reduced by CMS nor did UFP-101 modify these parameters. DISCUSSION AND

conclusionThis study demonstrated that chronic treatment with UFP-101 produces antidepressant-like effects in rats subjected to CMS supporting the proposal that NOP receptors represent a candidate target for the development of innovative antidepressant drugs.

Indexed as

Narcotic AntagonistsAnimalsAntidepressive AgentsBehavior, AnimalDepressionDisease Models, AnimalDose-Response Relationship, DrugImipramineMaleNociceptin ReceptorOpioid PeptidesRatsRats, WistarReceptors, OpioidStress, PsychologicalSucroseAntidepressive AgentsImipramineNarcotic AntagonistsNociceptin Receptor(Nphe(1),Arg(14),Lys(15))N-OFQ NH(2)Opioid PeptidesOprl1 protein, ratReceptors, OpioidSucrose

Identifiers

PMID19711054
OpenAlexW2081739783

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.