Evidence map›Paper›PMID 32001238›Full record

ArticleNeuropharmacology2020

Female and male rats readily consume and prefer oxycodone to water in a chronic, continuous access, two-bottle oral voluntary paradigm.

Giulia Zanni, Matthew J DeSalle, Hannah M Deutsch, Gordon A Barr, Amelia J Eisch

Open access · greenAbstract read
In one paragraph

Article in Neuropharmacology, 2020. 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
2.7field-weighted citation impact, top 9% 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, 47 citations in OpenAlex.

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  16. Oral self-administration of pregabalin in a mouse model and the resulting drug addiction features.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
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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

5 authors at 1 institution in 1 country.

Giulia ZanniDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA. Electronic address: giulia.zanni@nyspi.columbia.edu.
Matthew J DeSalleDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA. Electronic address: desallem7@gmail.com.
Hannah M DeutschDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA. Electronic address: hdeutsch1@sas.penn.edu.
Gordon A BarrDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA; Department of Psychology, University of Pennsylvania, Philadelphia, PA, 19104, USA. Electronic address: barrg@chop.edu.
Amelia J EischDepartment of Anesthesiology and Critical Care, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA; Department of Neuroscience, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA. Electronic address: eisch@upenn.edu.
Children's Hospital of Philadelphia · US

Funding

New Horizons in Adult NeurogenesisK02DA023555 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI EISCH, AMELIA J · 2007 to 2017
$1.1M
NIDA NIH HHS K02 DA023555
6 · The paper itself

Abstract

The increasing abuse of opioids - such as oxycodone - poses major challenges for health and socioeconomic systems. Human prescription opioid abuse is marked by chronic, voluntary, oral intake and sex differences. To develop interventions, the field would benefit from a preclinical paradigm that similarly provides rodents with chronic, continuous, oral, voluntary and free-choice access to oxycodone. Here we show female and male rats voluntarily ingest and choose oxycodone over water and show both dependence and motivation to take oxycodone during a chronic oral voluntary, two-bottle choice, continuous access paradigm. Adult female and male Long-Evans rats were given unlimited, continuous homecage access to two bottles containing water (Control) or one bottle of water and one bottle of oxycodone dissolved in water (Experimental). Virtually all experimental rats voluntarily drank oxycodone (~10 mg/kg/day) and escalated their intake over 22 weeks. Females self-administered twice as much oxycodone by body weight (leading to higher blood levels of oxycodone) and engaged in more gnawing behavior of wooden blocks relative to males. Precipitated withdrawal revealed high levels of dependence in both sexes. Reflecting motivation to drink oxycodone, ascending concentrations of citric acid suppressed the intake of oxycodone (Experimental) and the intake of water (Control); however, Experimental rats returned to pre-citric acid preference levels whereas Controls rats did not. Pre-screening behaviors of rats on open field exploration predicted oxycodone intake. Thus, rats consumed and preferred oxycodone over time in this chronic two-bottle oral choice paradigm and both sexes displayed many features of human oxycodone abuse.

Indexed as

Sex CharacteristicsAdministration, OralAnalgesics, OpioidAnimalsChoice BehaviorDose-Response Relationship, DrugDrug Administration ScheduleFemaleMaleOpioid-Related DisordersOxycodoneRatsRats, Long-EvansSelf AdministrationSubstance Withdrawal SyndromeWaterAnalgesics, OpioidOxycodoneWaterDependenceEndophenotypeMotivationOpioidSelf-administrationSex difference

Identifiers

PMID32001238
PMCPMC9748519
OpenAlexW3003994338

What Socratic 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 Socratic graph.