Evidence map›Paper›PMID 24221825›Full record

ArticlePsychopharmacology2014

Extended access oxycodone self-administration and neurotransmitter receptor gene expression in the dorsal striatum of adult C57BL/6 J mice.

Yong Zhang, Brandan Mayer-Blackwell, Stefan D Schlussman, Matthew Randesi, Eduardo R Butelman, Ann Ho, Jurg Ott, Mary Jeanne Kreek

Abstract read
In one paragraph

Article in Psychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

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  9. Animal Models of the Behavioral Symptoms of Substance Use Disorders.Cold Spring Harbor perspectives in medicine · 2021
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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

8 authors at 2 institutions in 3 countries.

Yong ZhangLaboratory of the Biology of Addictive Diseases, Rockefeller University, 1230 York Avenue, Box 171, New York, NY, 10065, USA, zhangyo@rockefeller.edu.
Brandan Mayer-Blackwell
Stefan D Schlussman
Matthew Randesi
Eduardo R Butelman
Ann Ho
Jurg Ott
Mary Jeanne Kreek
Rockefeller University · USCzech Academy of Sciences, Institute of Psychology · CZ

Funding

Adolescent Oxycodone Self Administration and Vulnerability to Opiate AbuseR01DA029147 · NIDA · ROCKEFELLER UNIVERSITY · PI ZHANG, YONG · 2011 to 2014
$1.4M
NIDA NIH HHS 1R01DA029147-01A1NIDA NIH HHS DA05030NIDA NIH HHS R01 DA029147
6 · The paper itself

Abstract

rationaleAlthough non-medical use of oxycodone continues to be a growing problem in the United States, there are no animal studies examining the effects of long-term oxycodone self-administration (SA).

objectivesThe current study was designed to examine chronic oxycodone SA by mice (14 days), in novel extended (4 h) SA sessions and its effect on selective striatal neurotransmitter receptor mRNA expression.

methodsAdult male C57/BL6J mice were either allowed to self-administer oxycodone (0.25 mg/kg/infusion, FR1) or served as yoked-saline controls in an extended access paradigm. Mice self-administered oxycodone for 4 h/day for 14 consecutive days. Comparison groups with 14-days exposure to 1-h SA sessions were also studied. Within 1 h of the last extended SA session, mice were sacrificed, dorsal striatum was isolated and selective neurotransmitter receptor mRNA levels were examined.

resultsThe oxycodone groups poked the active hole significantly more times than the yoked controls. The number of nose pokes at the active hole rose over the 14 days in the oxycodone group with extended access. The expression of 13 neurotransmitter receptor mRNAs was significantly altered in the dorsal striatum, including the gamma-aminobutyric acid (GABA) A receptor beta 2 subunit (Gabrb2) showing experiment-wise significant decrease, as a result of extended oxycodone SA.

conclusionC57BL/6 J mice escalated the amount of oxycodone self-administered across 14 consecutive daily extended sessions, but not 1-h sessions. Decreases in Gabrb2 mRNA levels may underlie escalation of oxycodone intake in the extended access SA sessions.

Indexed as

AnimalsConditioning, OperantCorpus StriatumGene ExpressionMaleMiceMice, Inbred C57BLOxycodoneReceptors, GABAReceptors, GABA-AReceptors, NeurotransmitterSelf AdministrationTime FactorsGabrb2 protein, mouseOxycodoneReceptors, GABAReceptors, GABA-AReceptors, Neurotransmitter

Identifiers

PMID24221825
PMCPMC3954898
OpenAlexW2009794137

What OpenQuestion holds

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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.