Evidence map›Paper›PMID 24236888›Full record

ArticleAlcoholism, clinical and experimental research2014

Differential role of D1 and D2 receptors in the perifornical lateral hypothalamus in controlling ethanol drinking and food intake: possible interaction with local orexin neurons.

Yu-Wei Chen, Irene Morganstern, Jessica R Barson, Bartley G Hoebel, Sarah F Leibowitz

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. The Role of Dorsal Hippocampal Dopamine D1-Type Receptors in Social Learning, Social Interactions, and Food Intake in Male and Female Mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Article
  7. Article
  8. Hypothalamic neuropeptide signaling in alcohol addiction.Progress in neuro-psychopharmacology & biological psychiatry · 2016
    Review
  9. Article
  10. Article
  11. Review
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

5 authors at 2 institutions in 1 country.

Yu-Wei ChenDepartment of Psychology , Princeton University, Princeton, New Jersey; Laboratory of Behavioral Neurobiology , The Rockefeller University, New York, New York.
Irene Morganstern
Jessica R Barson
Bartley G Hoebel
Sarah F Leibowitz
Rockefeller University · USPrinceton University · US

Funding

HYPOTHALAMIC PEPTIDES IN THE CONTROL OF ALCOHOL INTAKER01AA012882 · NIAAA · ROCKEFELLER UNIVERSITY · PI LEIBOWITZ, SARAH F. · 2001 to 2015
$4.0M
NIAAA NIH HHS AA12882NIAAA NIH HHS R01 AA012882
6 · The paper itself

Abstract

backgroundThe neurotransmitter dopamine (DA), acting in various mesolimbic brain regions, is well known for its role in promoting motivated behaviors, including ethanol (EtOH) drinking. Indirect evidence, however, suggests that DA in the perifornical lateral hypothalamus (PF/LH) has differential effects on EtOH consumption, depending on whether it acts on the DA 1 (D1) or DA 2 (D2) receptor subtype, and that these effects are mediated in part by local peptide systems, such as orexin/hypocretin (OX) and melanin-concentrating hormone (MCH), known to stimulate the consumption of EtOH.

methodsThe present study in brain-cannulated Sprague-Dawley rats measured the effects of dopaminergic compounds in the PF/LH on drinking behavior in animals trained to consume 7% EtOH and also on local peptide mRNA expression using digoxigenin-labeled in situ hybridization in EtOH-naïve animals.

resultsExperiments 1 and 2 showed that the D1 agonist SKF81297 (10.8 nmol/side) in the PF/LH significantly increased food intake, while tending to increase EtOH intake, and the D1 antagonist SCH23390 significantly decreased EtOH intake without affecting food intake. In contrast, the D2 agonist quinelorane (6.2 nmol/side) in the PF/LH significantly reduced EtOH consumption, while the D2 antagonist sulpiride increased it. Experiments 3 and 4 revealed differential effects of PF/LH injection of the DA agonists on local OX mRNA, which was increased by the D1 agonist and decreased by the D2 agonist. These DA agonists had no impact on MCH expression.

conclusionsThese results support a stimulatory role of the PF/LH D1 receptor in promoting the consumption of both EtOH and food, in contrast to a suppressive effect of the D2 receptor on EtOH drinking. They further suggest that these receptors affect consumption, in part, through local OX-expressing neurons. These findings provide new evidence for the function of PF/LH DA receptor subtypes in controlling EtOH and food intake.

Indexed as

Alcohol DrinkingAnimalsEatingHypothalamic HormonesHypothalamusIn Situ HybridizationIntracellular Signaling Peptides and ProteinsMaleMelaninsNeuropeptidesOrexin ReceptorsOrexinsPituitary HormonesRatsRats, Sprague-DawleyReceptors, Dopamine D1Hypothalamic HormonesIntracellular Signaling Peptides and Proteinsmelanin-concentrating hormoneMelaninsNeuropeptidesOrexin ReceptorsOrexinsPituitary HormonesReceptors, Dopamine D1Receptors, Dopamine D2DopamineEthanolLateral HypothalamusMelanin-Concentrating HormoneOrexin

Identifiers

PMID24236888
PMCPMC4203365
OpenAlexW2018549693

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.