Evidence map›Paper›PMID 26142563›Full record

ArticleAlcohol (Fayetteville, N.Y.)2015

Lack of effect of nucleus accumbens dopamine D1 receptor blockade on consumption during the first two days of operant self-administration of sweetened ethanol in adult Long-Evans rats.

James M Doherty, Rueben A Gonzales

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

2 authors at 1 institution in 1 country.

James M DohertyWaggoner Center for Alcohol and Addiction Research, University of Texas at Austin, Austin, TX 78712, USA; Department of Pharmacology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA.
Rueben A GonzalesWaggoner Center for Alcohol and Addiction Research, University of Texas at Austin, Austin, TX 78712, USA; Department of Pharmacology, College of Pharmacy, University of Texas at Austin, Austin, TX 78712, USA. Electronic address: rgonzales@austin.utexas.edu.
The University of Texas at Austin · US

Funding

Neurochemical & Behavioral Correlates of ETOH EffectsT32AA007471 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI Kimberly Nixon · 1987 to 2026
$9.2M
Neurochemical mechanisms of ethanol self-administrationR37AA011852 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI GONZALES, RUEBEN A. · 2009 to 2018
$2.8M
NIAAA NIH HHS R37 AA011852NIAAA NIH HHS R37 AA11852NIAAA NIH HHS T32 AA00747NIAAA NIH HHS T32 AA007471
6 · The paper itself

Abstract

The mechanisms underlying ethanol self-administration are not fully understood; however, it is clear that ethanol self-administration stimulates nucleus accumbens dopamine release in well-trained animals. During operant sweetened ethanol self-administration behavior, an adaptation in the nucleus accumbens dopamine system occurs between the first and second exposure, paralleling a dramatic increase in sweetened ethanol intake, which suggests a single exposure to sweetened ethanol may be sufficient to learn the association between sweetened ethanol cues and its reinforcing properties. In the present experiment, we test the effects of blockade of nucleus accumbens dopamine D1 receptors on operant sweetened ethanol self-administration behavior during the first 2 days of exposure. Adult male Long-Evans rats were first trained to self-administer 10% sucrose (10S) across 6 days in an appetitive and consummatory operant model (appetitive interval: 10-min pre-drinking wait period and a lever response requirement of 4; consummatory interval: 20-min access to the drinking solution). After training on 10S, the drinking solution was switched to 10% sucrose plus 10% ethanol (10S10E); control rats continued drinking 10S throughout the experiment. Bilateral nucleus accumbens microinjections of the dopamine D1 antagonist, SCH-23390 (0, 1.0, or 3.0 μg/side), immediately preceded the first two sessions of drinking 10S10E. Results show that blocking nucleus accumbens dopamine D1 receptors has little or no influence on consumption during the first 2 days of exposure to the sweetened ethanol solution or maintenance of sucrose-only drinking. Furthermore, the high dose of SCH-23390, 3.0 μg/side, reduced open-field locomotor activity. In conclusion, we found no evidence to suggest that nucleus accumbens D1 receptor activation is involved in consumption of a sweetened ethanol solution during the first 2 days of exposure or maintenance of sucrose drinking, but rather D1 receptors seem necessary for general locomotor activity that contributes to initiation of appetitive behavior.

Indexed as

Alcohol DrinkingAnimalsBenzazepinesConditioning, OperantDopamine AntagonistsEthanolMaleNucleus AccumbensRatsRats, Long-EvansReceptors, Dopamine D1Self AdministrationSweetening AgentsBenzazepinesDopamine AntagonistsEthanolReceptors, Dopamine D1SCH 23390Sweetening AgentsAlcoholDopamineEthanolInitiationMicroinjectionNucleus accumbens

Identifiers

PMID26142563
PMCPMC4554881
OpenAlexW2099911841

What OpenQuestion holds

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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.