Evidence map›Paper›PMID 30970376›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

Effects of stimulation of mu opioid and nociceptin/orphanin FQ peptide (NOP) receptors on alcohol drinking in rhesus monkeys.

Shawn M Flynn, Phillip M Epperly, April T Davenport, Gerta Cami-Kobeci, Stephen M Husbands, Mei-Chuan Ko, Paul W Czoty

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. PET Imaging of [Molecules (Basel, Switzerland) · 2020
    Article
  11. Effects of NOP-Related Ligands in Nonhuman Primates.Handbook of experimental pharmacology · 2019
    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.

Shawn M FlynnDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Phillip M EpperlyDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
April T DavenportDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Gerta Cami-KobeciDepartment of Pharmacy and Pharmacology, University of Bath, Bath, BA2 7AY, UK.
Stephen M HusbandsDepartment of Pharmacy and Pharmacology, University of Bath, Bath, BA2 7AY, UK.
Mei-Chuan KoDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.ORCID http://orcid.org/0000-0003-2436-4506
Paul W CzotyDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. pczoty@wakehealth.edu.
Wake Forest University · USUniversity of Bath · GB

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jeffrey L. Weiner · 2018 to 2026
$16.2M
Narcotic Drug and Opioid Peptide Basic Research projectP01DA000254 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WOODS, JAMES H · 2003 to 2006
$5.0M
DISCOVERY OF NEW TREATMENTS FOR INTRAVENOUS DRUG ABUSER01DA007315 · NIDA · UNIVERSITY OF BRISTOL · PI HUSBANDS, STEPHEN M, TRAYNOR, JOHN R. · 1991 to 2019
$4.8M
Translational Studies on Early-life Stress and Vulnerability to Alcohol AddictionP01AA021099 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINER, JEFFREY L. · 2012 to 2016
$2.8M
NIAAA NIH HHS P01 AA021099NIAAA NIH HHS P50 AA026117NIDA NIH HHS P01 DA000254NIDA NIH HHS R01 DA007315
6 · The paper itself

Abstract

Alcohol use disorder (AUD) persists as a devastating public health problem; widely effective pharmacological treatments are needed. Evidence from rodent models suggests that stimulating brain receptors for the neuropeptide nociceptin/orphanin FQ (NOP) can decrease ethanol drinking. We characterized the effects of the mu opioid peptide (MOP) receptor agonist buprenorphine and the buprenorphine analog (2S)-2-[(5R,6R,7R,14S)-N-cyclopropylmethyl-4,5-epoxy-6,14-ethano-3-hydroxy-6 methoxymorphinan-7-yl]-3,3-dimethylpentan-2-ol (BU08028), which stimulates MOP and NOP receptors, in a translational nonhuman primate model of AUD. Rhesus monkeys drank a 4% ethanol solution 6 h per day, 5 days per week via an operant behavioral panel in their home cages. To assess behavioral selectivity, monkeys responded via a photo-optic switch to earn food pellets. After characterizing the acute effects of BU08028 (0.001-0.01 mg/kg, i.m.) and buprenorphine (0.003-0.056 mg/kg, i.m.), the drugs were administered chronically using a model of pharmacotherapy assessment that incorporates clinical aspects of AUD and treatment. Acutely, both drugs decreased ethanol drinking at doses that did not affect food-maintained responding. During chronic treatment, effects of BU08028 and buprenorphine were maintained for several weeks without development of tolerance or emergence of adverse effects. BU08028 was ~0.5 and 1.0 log units more potent in acute and chronic studies, respectively. The selective NOP receptor agonist SCH 221510 also selectively decreased ethanol intakes when given acutely (0.03-1.0 mg/kg, i.m.), whereas the MOP antagonist naltrexone (1.7-5.6 mg/kg, i.m.) decreased both ethanol intake and food pellets delivered. These data demonstrate that bifunctional MOP/NOP agonists, which may have therapeutic advantages to MOP-selective drugs, can decrease alcohol drinking in nonhuman primates.

Indexed as

Alcohol DrinkingAnimalsAzabicyclo CompoundsBuprenorphineDose-Response Relationship, DrugEatingMacaca mulattaMaleNaltrexoneNociceptin ReceptorReceptors, OpioidReceptors, Opioid, mu2-(N-cyclopropylmethyl-4,5-epoxy-6,14-ethano-3-hydroxy-6-methoxymorphinan-7-yl)-3,3-dimethylpentan-2-ol8-(bis(2-methylphenyl)methyl)-3-phenyl-8-azabicyclo(3.2.1)octan-3-olAzabicyclo CompoundsBuprenorphineNaltrexoneNociceptin ReceptorReceptors, OpioidReceptors, Opioid, mu

Identifiers

PMID30970376
PMCPMC6784996
OpenAlexW2936340882

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.