Evidence map›Paper›PMID 21803530›Full record

ArticleAlcohol (Fayetteville, N.Y.)2011

Increased consumption of ethanol and sugar water in mice lacking the dopamine D2 long receptor.

Zachary B Bulwa, Jordan A Sharlin, Peter J Clark, Tushar K Bhattacharya, Chessa N Kilby, Yanyan Wang, Justin S Rhodes

Open access · greenAbstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
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  5. Article
  6. FACTORS CONTRIBUTING TO THE ESCALATION OF ALCOHOL CONSUMPTION.Neuroscience and biobehavioral reviews · 2022
    Review
  7. Genetics of mouse behavioral and peripheral neural responses to sucrose.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Genes and Alcohol Consumption: Studies with Mutant Mice.International review of neurobiology · 2016
    Review
  18. Article
  19. Article
  20. Upregulation of dopamine D2 receptors in the nucleus accumbens indirect pathway increases locomotion but does not reduce alcohol consumption.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    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

7 authors at 1 institution in 1 country.

Zachary B BulwaDepartment of Molecular and Cellular Biology, Beckman Institute, University of Illinois, Urbana, IL 61801, USA.
Jordan A Sharlin
Peter J Clark
Tushar K Bhattacharya
Chessa N Kilby
Yanyan Wang
Justin S Rhodes
University of Illinois Urbana-Champaign · US

Funding

Mouse genetic differences in exercise-induced hippocampal neurogenesis & learningR01MH083807 · NIMH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI RHODES, JUSTIN S · 2009 to 2013
$1.4M
The functional significance of exercise-induced neurogenesis in cocaine rewardR01DA027487 · NIDA · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI RHODES, JUSTIN S · 2009 to 2013
$1.3M
NIDA NIH HHS DA027487NIDA NIH HHS R01 DA027487NIMH NIH HHS MH083807NIMH NIH HHS R01 MH083807
6 · The paper itself

Abstract

Individual differences in dopamine D2 receptor (D2R) expression in the brain are thought to influence motivation and reinforcement for ethanol and other rewards. D2R exists in two isoforms, D2 long (D2LR) and D2 short (D2SR), produced by alternative splicing of the same gene. The relative contributions of D2LR versus D2SR to ethanol and sugar water drinking are not known. Genetic engineering was used to produce a line of knockout (KO) mice that lack D2LR and consequently have increased expression of D2SR. KO and wild-type (WT) mice of both sexes were tested for intake of 20% ethanol, 10% sugar water and plain tap water using established drinking-in-the-dark procedures. Mice were also tested for effects of the D2 antagonist eticlopride on intake of ethanol to determine whether KO responses were caused by lack of D2LR or overrepresentation of D2SR. Locomotor activity on running wheels and in cages without wheels was also measured for comparison. D2L KO mice drank significantly more ethanol than WT in both sexes. KO mice drank more sugar water than WT in females but not in males. Eticlopride dose dependently decreased ethanol intake in all groups except male KO. KO mice were less physically active than WT in cages with or without running wheels. Results suggest that overrepresentation of D2SR contributes to increased intake of ethanol in the KO mice. Decreasing wheel running and general levels of physical activity in the KO mice rules out the possibility that higher intake results from higher motor activity. Results extend the literature implicating altered expression of D2R in risk for addiction by delineating the contribution of individual D2R isoforms. These findings suggest that D2LR and D2SR play differential roles in consumption of alcohol and sugar rewards.

Indexed as

AlcoholismAlternative SplicingAnimalsCarbohydratesDopamine AntagonistsEthanolFemaleMaleMiceMice, Inbred C57BLMice, KnockoutMotor ActivityProtein IsoformsReceptors, Dopamine D2SalicylamidesSolutionsCarbohydratesDopamine AntagonistsEthanoleticloprideProtein IsoformsReceptors, Dopamine D2SalicylamidesSolutionsWater

Identifiers

PMID21803530
PMCPMC3184387
OpenAlexW2108509636

What OpenQuestion 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 OpenQuestion graph.