Evidence map›Paper›PMID 27567437›Full record

ArticleDrug and alcohol dependence2016

Cocaine self-administration and reinstatement in female rats selectively bred for high and low voluntary running.

J R Smethells, N E Zlebnik, D K Miller, M J Will, F Booth, M E Carroll

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. (±)VK4-40, a novel dopamine DBritish journal of pharmacology · 2020
    Article
  4. Article
  5. 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

6 authors.

J R SmethellsDepartment of Psychiatry, University of Minnesota Medical School, Minneapolis, MN, United States. Electronic address: jsmethells@gmail.com.
N E ZlebnikDepartment of Psychiatry, University of Minnesota Medical School, Minneapolis, MN, United States.
D K MillerDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States.
M J WillDepartment of Psychological Sciences, University of Missouri, Columbia, MO, United States.
F BoothDepartment of Medical Pharmacology and Physiology, University of Missouri, Columbia, MO, United States; Department of Biomedical Science, University of Missouri, Columbia, MO, United States, United States; Dalton Cardiovascular Research Center, University of Missouri, Columbia, MO, United States; Department of Nutrition and Exercise Physiology, University of Missouri, Columbia, MO, United States.
M E CarrollDepartment of Psychiatry, University of Minnesota Medical School, Minneapolis, MN, United States.

Funding

Training in PharmacoNeuroImmune Substance Abuse ResearchT32DA007097 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MOLITOR, THOMAS WILLIAM · 1985 to 2021
$13.1M
Statistical Analysis CoreP50DA033942 · NIDA · UNIVERSITY OF MINNESOTA · PI CARROLL, MARILYN E. · 2012 to 2017
$6.3M
PREDOCTORAL TRAINING OF NEUROSCIENTISTST32GM008471 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI EBNER, TIMOTHY J · 1993 to 2017
$4.9M
NIDA NIH HHS P50 DA033942NIDA NIH HHS T32 DA007097NIGMS NIH HHS T32 GM008471
6 · The paper itself

Abstract

backgroundPrevious research has found that rats behaviorally screened for high (vs. low) wheel running were more vulnerable to cocaine abuse. To assess the extent to which a genetic component is involved in this drug-abuse vulnerability, rats selectively bred for high or low voluntary running (HVR or LVR, respectively) were examined for differences in cocaine seeking in the present study.

methodsFemale rats were trained to lever press for food and then were assessed for differences in acquisition of cocaine (0.4mg/kg; i.v.) self-administration across 10 sessions. Once acquired, rats self-administered cocaine for a 14-day maintenance phase, followed by a 14-day extinction phase when cocaine was no longer available. Subsequently, reinstatement of cocaine seeking was examined with priming injections of cocaine (5, 10 & 15mg/kg), caffeine (30mg/kg), yohimbine (2.5mg/kg) and cocaine-paired cues.

resultsA greater percentage of LVR rats met the acquisition criteria for cocaine self-administration and in fewer sessions than HVR rats. No differences in responding for cocaine were observed between phenotypes during maintenance. However, during extinction LVR rats initially responded at higher rates and persisted in cocaine seeking for a greater number of sessions. No phenotype differences were observed following drug and cue-primed reinstatement of cocaine seeking.

conclusionsIn general, LVR rats were more sensitive to the reinforcing effects of cocaine than HVR rats during periods of transition into and out of cocaine self-administration. Thus, LVR rats sometimes showed a greater vulnerability cocaine seeking than HVR rats.

Indexed as

Reinforcement, PsychologySelf AdministrationAdrenergic alpha-2 Receptor AntagonistsAnimalsCaffeineCentral Nervous System StimulantsCocaineCocaine-Related DisordersCuesExtinction, PsychologicalFemaleMotor ActivityRatsRats, Sprague-DawleyRats, WistarRunningAdrenergic alpha-2 Receptor AntagonistsCaffeineCentral Nervous System StimulantsCocaineYohimbineAcquisitionCocaine self-administrationExtinctionPhenotypeRatsWheel running

Identifiers

PMID27567437
PMCPMC5037047

What OpenQuestion holds

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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.