Evidence map›Paper›PMID 37461188›Full record

ArticleGenes, brain, and behavior2023

Patterns of ethanol intake in male rats with partial dopamine transporter deficiency.

L B Kuiper, J B Roberts, P M Estave, D Leo, R R Gainetdinov, S R Jones

Open access · hybridAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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 at 3 institutions in 3 countries.

L B KuiperDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0002-0268-5133
J B RobertsDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
P M EstaveDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
D LeoDepartment of Neurosciences, University of Mons, Mons, Belgium.
R R GainetdinovInstitute of Translational Biomedicine, St. Petersburg State University, St. Petersburg, Russia.
S R JonesDepartment of Physiology and Pharmacology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Wake Forest University · USSt Petersburg University · RUUniversity of Mons · BE

Funding

Wake Forest Translational Alcohol Research Center (WF-TARC)P50AA026117 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Colleen A Hanlon · 2018 to 2026
$16.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
Role of Kappa Opioid Receptors in Maladaptive Catecholamine Responses to Stress and Alcohol ExposureU01AA014091 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Katherine Mercedes Holleran, SARA RAULERSON JONES · 2003 to 2026
$7.7M
Kappa Opioid Receptors and Phospho-Dopamine Transporters Drive Cocaine RewardR01DA054694 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI LANKUPALLE D JAYANTHI, SARA RAULERSON JONES · 2022 to 2026
$3.2M
The Neurobiology of Drug AbuseT32DA041349 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SARA RAULERSON JONES · 2017 to 2026
$1.8M
NIAAA NIH HHS AA007565NIAAA NIH HHS AA026117NIAAA NIH HHS P50 AA026117NIAAA NIH HHS T32 AA007565NIAAA NIH HHS U01 AA014091NIDA NIH HHS R01 DA054694NIDA NIH HHS T32 DA041349
6 · The paper itself

Abstract

Mesolimbic dopamine signaling plays a major role in alcohol and substance use disorders as well as comorbidities such as anxiety and depression. Growing evidence suggests that alcohol drinking is modulated by the function of the dopamine transporter (DAT), which tightly regulates extracellular dopamine concentrations. Adult male rats on a Wistar Han background (DAT+/+) and rats with a partial DAT deletion (DAT+/-) were used in this study. First, using fast-scan cyclic voltammetry in brain slices containing the nucleus accumbens core from ethanol-naïve subjects, we measured greater evoked dopamine concentrations and slower dopamine reuptake in DAT+/- rats, consistent with increased dopamine signaling. Next, we measured ethanol drinking using the intermittent access two-bottle choice paradigm (20% v/v ethanol vs. water) across 5 weeks. DAT+/- rats voluntarily consumed less ethanol during its initial availability (the first 30 min), especially after longer periods of deprivation. In addition, DAT+/- males consumed less ethanol that was adulterated with the bitter tastant quinine. These findings suggest that partial DAT blockade and concomitant increase in brain dopamine levels has potential to reduce drinking and ameliorate alcohol use disorder (AUD).

Indexed as

Dopamine Plasma Membrane Transport ProteinsEthanolAlcohol DrinkingAnimalsDopamineHumansMaleNucleus AccumbensRatsRats, WistarDopamineDopamine Plasma Membrane Transport ProteinsEthanolalcohol use disorderbingedopaminedopamine transporterdrinkingethanolfast-scan cyclic voltammetryhypodopaminergiaintermittent accesslocomotor activitynoveltynucleus accumbensquininereuptakeWistar

Identifiers

PMID37461188
PMCPMC10733570
OpenAlexW4384627343

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.