Evidence map›Paper›PMID 25811380›Full record

ArticlePloS one2015

Central melanocortins regulate the motivation for sucrose reward.

Rahul Pandit, Esther M van der Zwaal, Mieneke C M Luijendijk, Maike A D Brans, Andrea J van Rozen, Ralph J A Oude Ophuis, Louk J M J Vanderschuren, Roger A H Adan, Susanne E la Fleur

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Rahul PanditDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Esther M van der ZwaalDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Mieneke C M LuijendijkDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Maike A D BransDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Andrea J van RozenDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Ralph J A Oude OphuisDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Louk J M J VanderschurenDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands; Department of Animals in Science and Society, Division of Behavioural Neuroscience, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Roger A H AdanDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Susanne E la FleurDepartment of Translational Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands; Department of Endocrinology and Metabolism, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
University Medical Center Utrecht · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the melanocortin (MC) system in feeding behavior is well established. Food intake is potently suppressed by central infusion of the MC 3/4 receptor agonist α-melanocyte stimulating hormone (α-MSH), whereas the MC 3/4 receptor inverse-agonist Agouti Related Peptide (AGRP) has the opposite effect. MC receptors are widely expressed in both hypothalamic and extra-hypothalamic brain regions, including nuclei involved in food reward and motivation, such as the nucleus accumbens (NAc) and the ventral tegmental area. This suggests that MCs modulate motivational aspects of food intake. To test this hypothesis, rats were injected intracerebroventricularly with α-MSH or AGRP and their motivation for sucrose was tested under a progressive ratio schedule of reinforcement. Food motivated behavior was dose-dependently decreased by α-MSH. Conversely, AGRP increased responding for sucrose, an effect that was blocked by pretreatment with the dopamine receptor antagonist α-flupenthixol. In contrast to progressive ratio responding, free intake of sucrose remained unaltered upon α-MSH or AGRP infusion. In addition, we investigated whether the effects of α-MSH and AGRP on food motivation were mediated by the NAc shell. In situ hybridization of MC3 and MC4 receptor expression confirmed that the MC4 receptor was expressed throughout the NAc, and injection of α-MSH and AGRP into the NAc shell caused a decrease and an increase in motivation for sucrose, respectively. These data show that the motivation for palatable food is modulated by MC4 receptors in the NAc shell, and demonstrate cross-talk between the MC and dopamine system in the modulation of food motivation.

Indexed as

RewardAgouti-Related Proteinalpha-MSHAnimalsCentral Nervous SystemFeeding BehaviorMaleMelanocortinsMotivationNucleus AccumbensRats, WistarReceptor, Melanocortin, Type 3Receptor, Melanocortin, Type 4Signal TransductionSucroseAgouti-Related Proteinalpha-MSHMelanocortinsReceptor, Melanocortin, Type 3Receptor, Melanocortin, Type 4Sucrose

Identifiers

PMID25811380
PMCPMC4374756
OpenAlexW2158339463

What OpenQuestion holds

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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.