Evidence map›Paper›PMID 22342812›Full record

ArticlePhysiology & behavior2012

Melanocortin 4 receptor signaling in dopamine 1 receptor neurons is required for procedural memory learning.

Huxing Cui, Brittany L Mason, Charlotte Lee, Akinori Nishi, Joel K Elmquist, Michael Lutter

Registry-linked trialAbstract read
In one paragraph

Article in Physiology & behavior, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03766191 (The Relation of Genetic Factors, Food Cues, and Self-Regulation With Excess Consumption and Adiposity in Children), which is not on this map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-weighted citation impact, top 7% 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.

NCT03766191 nacompletednot on this mapstarted 2019, after this paper: background citation

The Relation of Genetic Factors, Food Cues, and Self-Regulation With Excess Consumption and Adiposity in Children

TypeinterventionalSponsorTrustees of Dartmouth CollegeRan2019 to 2024Enrolled189ConditionsChildhood ObesityArmsFood Ads, Non-food Ads
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 48 citations in OpenAlex.

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  6. Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
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  7. Review
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  15. Cross interaction of melanocortinergic and dopaminergic systems in neural modulation.International journal of physiology, pathophysiology and pharmacology · 2015
    Article
  16. MC4R expression in pedunculopontine nucleus involved in the modulation of midbrain dopamine system.International journal of clinical and experimental pathology · 2015
    Article
  17. Article
  18. Article
  19. Synaptic changes induced by melanocortin signalling.Nature reviews. Neuroscience · 2014
    Review
  20. 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 2 institutions in 2 countries.

Huxing CuiDepartment of Internal Medicine (Division of Hypothalamic Research), University of Texas Southwestern Medical Center Dallas, Dallas, TX 75390-9127, United States.
Brittany L Mason
Charlotte Lee
Akinori Nishi
Joel K Elmquist
Michael Lutter
The University of Texas Southwestern Medical Center · USKurume University · JP

Funding

Central Mechanisms Regulating Energy Homeostasis, Project 2 of 10RL1DK081185 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K. · 2007 to 2011
$3.8M
NEUROANATOMIC MECHANIMS OF LEPTIN ACTIONR01DK053301 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI ELMQUIST, JOEL K · 1998 to 2006
$3.0M
Mouse Phenotype Core, Project 9 of 10PL1DK081182 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI RUSSELL, DAVID W. · 2007 to 2011
$2.0M
Melanocortin Signaling in DepressionK08MH084058 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI LUTTER, MICHAEL · 2009 to 2013
$853k
NIDDK NIH HHS DK081182-01NIDDK NIH HHS DK081185-01NIDDK NIH HHS PL1 DK081182NIDDK NIH HHS R01 DK053301NIDDK NIH HHS R01DK53301NIDDK NIH HHS RL1 DK081185NIDDK NIH HHS RL1DK081185NIMH NIH HHS K08 MH084058NIMH NIH HHS MH084058-01A1
6 · The paper itself

Abstract

It is now widely recognized that exposure to palatable foods engages reward circuits that promote over-eating and facilitate the development of obesity. While the melanocortin 4 receptor (MC4R) has previously been shown to regulate food intake and energy expenditure, little is known about its role in food reward. We demonstrate that MC4R is co-expressed with the dopamine 1 receptor (D1R) in the ventral striatum. While MC4R-null mice are hyperphagic and obese, they exhibit impairments in acquisition of operant responding for a high fat reinforcement. Restoration of MC4R signaling in D1R neurons normalizes procedural learning without affecting motivation to obtain high fat diet. MC4R signaling in D1R neurons is also required for learning in a non-food-reinforced version of the cued water maze. Finally, MC4R signaling in neostriatal slices increases phosphorylation of the Thr34 residue of DARPP-32, a protein phosphatase-1 inhibitor that regulates synaptic plasticity. These data identify a novel requirement for MC4R signaling in procedural memory learning.

Indexed as

AnimalsConditioning, OperantDopamine and cAMP-Regulated Phosphoprotein 32Dopaminergic NeuronsFemaleMaleMaze LearningMemoryMiceMice, Inbred C57BLMice, TransgenicNeostriatumPhosphorylationReceptor, Melanocortin, Type 4Receptors, Dopamine D1Reinforcement, PsychologyDopamine and cAMP-Regulated Phosphoprotein 32Ppp1r1b protein, mouseReceptor, Melanocortin, Type 4Receptors, Dopamine D1

Identifiers

PMID22342812
PMCPMC3314089
OpenAlexW2087550438

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.