Evidence map›Paper›PMID 41554955›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

Modulation of accumbens dopamine by MCH neurons during learning and consummatory behavior.

Liam E Potter, Brandon A Toth, Jayeeta Manna, Lorelei Baron, Hannah C Lyons, Jack R Evans, Christian R Burgess

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Liam E PotterMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Brandon A TothMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0003-1046-6499
Jayeeta MannaMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Lorelei BaronMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Hannah C LyonsMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0009-0004-2491-7646
Jack R EvansMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA.
Christian R BurgessMichigan Neuroscience Institute, University of Michigan, Ann Arbor, MI, USA. crburge@umich.edu.ORCID http://orcid.org/0000-0001-6133-8089

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Elucidating the role for MCH neurons in feeding behavior and responses to sensory food cuesR01DK129366 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURGESS, CHRISTIAN RICHARD · 2021 to 2025
$2.1M
NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK129366U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1F31NS132434
6 · The paper itself

Abstract

The formation of sensory cue-reward associations is essential for survival, but in the modern calorie-rich and advertising-intensive environment, such associations may become maladaptive - leading to negative health consequences such as obesity or diabetes. Recent research has demonstrated the importance of hypothalamic melanin-concentrating hormone (MCH)-expressing neurons in driving hedonically-motivated feeding and in forming these associations. The MCH system interacts with mesolimbic dopamine (DA) transmission, offering a potential mechanism for the effects of MCH neurons on hedonic feeding and associative conditioning. However, this interaction has not been fully characterized in vivo with modern approaches that offer high temporal and spatial resolution. We characterized MCH-DA interactions during feeding and food-motivated Pavlovian conditioning using in vivo fiber photometry in the lateral hypothalamus/zona incerta (LH/ZI) and nucleus accumbens (NAc). We found that MCH neuron activity and DA release in the medial-shell of the NAc (mNAcSh) were co-activated during consumption and in response to reward-predicting cues. During consumption, DA release preceded MCH activity, while responses to reward-predicting cues emerged in MCH neurons earlier than in the DA system. Lastly, gain and loss-of function of the MCH system could bidirectionally modulate DA release in the mNAcSh. These results indicate that physiological co-activation of the MCH and DA systems occurs during food-motivated learning, and demonstrate a capacity for bidirectional modulation of DA release in the mNAcSh by the MCH system.

Indexed as

Conditioning, ClassicalConsummatory BehaviorDopamineHypothalamic HormonesMelaninsNeuronsNucleus AccumbensPituitary HormonesAnimalsMaleMesolimbic SystemRatsRats, Sprague-DawleyRewardDopamineHypothalamic Hormonesmelanin-concentrating hormoneMelaninsPituitary Hormones

Identifiers

PMID41554955
PMCPMC13212990

What OpenQuestion holds

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LicenceCC BY
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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.