Evidence map›Paper›PMID 36228740›Full record

ArticlePharmacology, biochemistry, and behavior2022

Sensitivity of a fentanyl-vs.-social interaction choice procedure to environmental and pharmacological manipulations.

Celsey M St Onge, Kaia M Taylor, Madison M Marcus, E Andrew Townsend

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Celsey M St OngeDepartment of Medicinal Chemistry, Virginia Commonwealth University, Richmond, VA, USA.
Kaia M TaylorDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA, USA.
Madison M MarcusDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA, USA.
E Andrew TownsendDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA, USA; Division of Therapeutics and Medical Consequences, National Institute on Drug Abuse, North Bethesda, MD, USA. Electronic address: drew.townsend@nih.gov.
Virginia Commonwealth University · US

Funding

VCU Center for Drug Addiction ResearchP30DA033934 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI YAN ZHANG · 2014 to 2026
$13.8M
Building Undergraduate Research Training as a Foundation for Diversifying Addiction ResearchR25DA051339 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI ADKINS, AMY ELIZABETH, CHARTIER, KAREN G. · 2021 to 2023
$486k
Exploiting Biased Agonism at the Ghrelin Receptor (GHSR1a) for Opioid AddictionF32DA051139 · NIDA · DUKE UNIVERSITY · PI GROSS, JOSHUA D · 2020 to 2022
$201k
Development of a Potential Treatment for Polysubstance Use DisordersF31DA054796 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI ST. ONGE, CELSEY MACKENNA · 2021 to 2022
$80k
NIDA NIH HHS F31 DA054796NIDA NIH HHS F32 DA051139NIDA NIH HHS P30 DA033934NIDA NIH HHS R25 DA051339
6 · The paper itself

Abstract

Recent studies have shown that social interaction can serve as an alternative reinforcer to opioid self-administration under a choice context in rats. However, additional parametric studies are needed to evaluate the sensitivity of opioid-vs.-social interaction procedures relative to more established opioid-vs.-food procedures. The current study evaluated the sensitivity of a novel fentanyl-vs.-social interaction choice procedure to environmental and pharmacological manipulations previously shown to affect fentanyl-vs.-food choice. Male and female rats (responder rats; n = 6/sex) were trained to respond in a discrete-trial choice procedure for either 30-s access to a same-sex "partner" rat or an intravenous fentanyl infusion. Once trained, the effects of fentanyl unit dose (0, 0.32-10 μg/kg/inf), partner rat presence, opioid-dependence status, chronic naltrexone administration (0.032, 0.1 mg/kg/h), and response requirement for fentanyl self-administration (fixed ratio 1-320) were determined across weeks. The fentanyl-vs.-social interaction choice procedure was sensitive to the unit dose of fentanyl, chronic naltrexone treatment, and fentanyl response requirement. However, the magnitude of these effects on fentanyl choice was smaller than those reported in published fentanyl-vs.-food choice studies. Furthermore, fentanyl-vs.-social interaction choice was not sensitive to removal of the partner rat or opioid-dependence status. Minimal sex differences were detected. These results suggest that this fentanyl-vs.-social interaction choice procedure is less sensitive to environmental and pharmacological interventions than previously established opioid-vs.-food choice procedures. The observed discrepancy in sensitivity between the procedures suggests that social interaction may have qualitatively different reinforcing properties compared to more commonly assessed alternative reinforcers such as food (preclinical) or money (human laboratory).

Indexed as

FentanylOpioid-Related DisordersAnalgesics, OpioidAnimalsDose-Response Relationship, DrugFemaleHumansMaleNaltrexoneRatsSelf AdministrationSocial InteractionAnalgesics, OpioidFentanylNaltrexoneChoiceFentanylOpioid withdrawalSelf-administrationSocial interaction

Identifiers

PMID36228740
PMCPMC9729431
OpenAlexW4303986006

What OpenQuestion holds

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Registered trials

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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.