Evidence map›Paper›PMID 37734282›Full record

ArticleDrug and alcohol dependence2023

Quantification of observable behaviors following oral administration of oxycodone and nalfurafine in male rhesus monkeys.

Sally L Huskinson, Donna M Platt, Zachary R Smith, William S Doyle, C Austin Zamarripa, Kristen Dunaway, Thomas E Prisinzano, Kevin B Freeman

Open access · greenAbstract read
In one paragraph

Article in Drug and alcohol dependence, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Using a rich-lean transition procedure to evaluate putative antianxiety medications.The Journal of pharmacology and experimental therapeutics · 2025
    Article
  3. 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

8 authors at 3 institutions in 1 country.

Sally L HuskinsonDivision of Neurobiology and Behavior Research, Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216. Electronic address: shuskinson@umc.edu.
Donna M PlattDivision of Neurobiology and Behavior Research, Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216.
Zachary R SmithDivision of Neurobiology and Behavior Research, Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA.
William S DoyleProgram in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216.
C Austin ZamarripaDepartment of Psychiatry and Behavioral Science, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
Kristen DunawayDivision of Neurobiology and Behavior Research, Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Thomas E PrisinzanoDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40506, USA.
Kevin B FreemanDivision of Neurobiology and Behavior Research, Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216.
University of Mississippi Medical Center · USJohns Hopkins University · USUniversity of Kentucky · US

Funding

Investigation of Neoclerodanes as Novel Opioid LigandsR01DA018151 · NIDA · UNIVERSITY OF KENTUCKY · PI PRISINZANO, THOMAS EDWARD · 2005 to 2020
$5.7M
Deterrents for prescription opioid abuseR01DA039167 · NIDA · UNIVERSITY OF MISSISSIPPI MED CTR · PI FREEMAN, KEVIN B. · 2015 to 2025
$4.9M
Benzodiazepine Choice and Polydrug UseR01DA054177 · NIDA · UNIVERSITY OF MISSISSIPPI MED CTR · PI Sally L Huskinson · 2022 to 2026
$2.5M
GABA-A receptor subtype mechanisms and the abuse-related effects of alcoholR01AA029023 · NIAAA · UNIVERSITY OF MISSISSIPPI MED CTR · PI PLATT, DONNA M · 2020 to 2024
$2.4M
Unpredictable availability as a determinant of drug-related outcomesR01DA045011 · NIDA · UNIVERSITY OF MISSISSIPPI MED CTR · PI HUSKINSON, SALLY · 2018 to 2022
$1.8M
Therapeutic selectivity of biased mu-opioid agonists.F31DA048586 · NIDA · UNIVERSITY OF MISSISSIPPI MED CTR · PI ZAMARRIPA, CARLOS AUSTIN · 2019 to 2021
$82k
NIAAA NIH HHS R01 AA029023NIDA NIH HHS F31 DA048586NIDA NIH HHS R01 DA018151NIDA NIH HHS R01 DA039167NIDA NIH HHS R01 DA045011NIDA NIH HHS R01 DA054177
6 · The paper itself

Abstract

backgroundRecent preclinical studies have investigated the atypical kappa-opioid receptor (KOR) agonist, nalfurafine, as a co-formulary with mu-opioid receptor (MOR) agonists as a potential deterrent for misuse. However, no study has investigated effects of nalfurafine combined with a MOR agonist using an oral route of administration. The objective of the current study was to measure behavioral effects of orally administered oxycodone and nalfurafine, alone and combined, in rhesus monkeys using a quantitative behavioral observation procedure.

methodsAdult male rhesus monkeys (N=5) were orally administered vehicle, oxycodone (0.56-1.8mg/kg), nalfurafine (0.001-0.0056mg/kg), or mixtures (1.0mg/kg oxycodone/0.001-0.0056mg/kg nalfurafine) in a Jell-O vehicle at multiple timepoints (10-320min). Species-typical and drug-induced behaviors were recorded by observers blinded to conditions.

resultsOxycodone alone significantly increased scratch and face-rub behaviors without affecting other behaviors. Nalfurafine decreased baseline levels of scratch without affecting other behaviors, and oxycodone-nalfurafine combinations resulted in reduced oxycodone-induced scratching at a dose (0.001mg/kg) that did not produce sedation-like effects. Oxycodone combined with larger nalfurafine doses (0.0032-0.0056mg/kg) also reduced oxycodone induced scratch that were accompanied with sedation-like effects (i.e., increased lip droop).

conclusionsNalfurafine was orally active in rhesus monkeys, and it reduced oxycodone-induced pruritus at a dose that did not produce sedation-like effects that are commonly observed with prototypical KOR agonists. Combinations of low doses of nalfurafine with MOR agonists such as oxycodone may be well-tolerated by humans who are prescribed MOR agonists for the treatment of pain.

Indexed as

OxycodoneReceptors, Opioid, kappaAdministration, OralAnalgesics, OpioidAnimalsHumansMacaca mulattaMaleMorphinansSpiro CompoundsAnalgesics, OpioidMorphinansOxycodoneReceptors, Opioid, kappaSpiro CompoundsTRK 820Kappa-opioid agonistMu-opioid agonistObservable behaviorOral administrationRhesus monkey

Identifiers

PMID37734282
PMCPMC10615792
OpenAlexW4386424279

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.