Evidence map›Paper›PMID 33837200›Full record

ArticleNature communications2021

Input-specific modulation of murine nucleus accumbens differentially regulates hedonic feeding.

Daniel J Christoffel, Jessica J Walsh, Boris D Heifets, Paul Hoerbelt, Sophie Neuner, Gordon Sun, Vinod K Ravikumar, Hemmings Wu, Casey H Halpern, Robert C Malenka

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

  1. Article
  2. Brain-wide activity mapping reveals the somatosensory cortex as a sex-specific regulator of hedonic feeding.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  3. Article
  4. Divergent Roles of Nucleus Accumbens D1- and D2-MSNs in Regulating Hedonic Feeding.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Sleep deprivation engages the orexin/hypocretin system to regulate food reward seeking.The international journal of neuropsychopharmacology · 2025
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

10 authors.

Daniel J ChristoffelNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.ORCID 0000-0002-6303-5134
Jessica J WalshNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Boris D HeifetsDepartment of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Paul HoerbeltNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Sophie NeunerNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Gordon SunNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Vinod K RavikumarDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.
Hemmings WuDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.
Casey H HalpernDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.
Robert C MalenkaNancy Pritzker Laboratory, Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA. malenka@stanford.edu.ORCID 0000-0002-5428-5211

Funding

Training CoreP50DA042012 · NIDA · STANFORD UNIVERSITY · PI Karl A. Deisseroth, Lisa Giocomo · 2017 to 2026
$27.1M
Interdisciplinary Research Training in Pain and Substance Use DisordersT32DA035165 · NIDA · STANFORD UNIVERSITY · PI SEAN C MACKEY · 2013 to 2026
$7.2M
Neural circuitry and synaptic physiology underlying MDMA's prosocial effectK08MH110610 · NIMH · STANFORD UNIVERSITY · PI HEIFETS, BORIS DOV · 2017 to 2020
$780k
Role of Nucleus Accumbens and Its Glutamatergic Inputs in High-Fat intakeR00DK115895 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHRISTOFFEL, DANIEL JOSEPH · 2021 to 2023
$736k
Role of Nucleus Accumbens and Its Glutamatergic Inputs in High-Fat intakeK99DK115895 · NIDDK · STANFORD UNIVERSITY · PI CHRISTOFFEL, DANIEL JOSEPH · 2018 to 2019
$182k
Systems level investigation of di-synaptic circuit involved in panic disorderF32MH103949 · NIMH · STANFORD UNIVERSITY · PI WALSH, JESSICA JILLIAN · 2014 to 2016
$126k
Function of thalamic excitatory synapses in social reward processingF32MH106206 · NIMH · STANFORD UNIVERSITY · PI CHRISTOFFEL, DANIEL JOSEPH · 2015 to 2017
$81k
NIDA NIH HHS P50 DA042012NIDA NIH HHS T32 DA035165NIDDK NIH HHS K99 DK115895NIDDK NIH HHS R00 DK115895NIMH NIH HHS F32 MH103949NIMH NIH HHS F32 MH106206NIMH NIH HHS K08 MH110610
6 · The paper itself

Abstract

Hedonic feeding is driven by the "pleasure" derived from consuming palatable food and occurs in the absence of metabolic need. It plays a critical role in the excessive feeding that underlies obesity. Compared to other pathological motivated behaviors, little is known about the neural circuit mechanisms mediating excessive hedonic feeding. Here, we show that modulation of prefrontal cortex (PFC) and anterior paraventricular thalamus (aPVT) excitatory inputs to the nucleus accumbens (NAc), a key node of reward circuitry, has opposing effects on high fat intake in mice. Prolonged high fat intake leads to input- and cell type-specific changes in synaptic strength. Modifying synaptic strength via plasticity protocols, either in an input-specific optogenetic or non-specific electrical manner, causes sustained changes in high fat intake. These results demonstrate that input-specific NAc circuit adaptations occur with repeated exposure to a potent natural reward and suggest that neuromodulatory interventions may be therapeutically useful for individuals with pathologic hedonic feeding.

Indexed as

RewardAnimal FeedAnimalsDietary FatsEatingFeeding BehaviorMaleMiceMice, TransgenicMicroscopy, ConfocalMidline Thalamic NucleiModels, AnimalMotivationNeural PathwaysNeuronal PlasticityNeuronsDietary FatsSlc17a6 protein, mouseVesicular Glutamate Transport Protein 2

Identifiers

PMID33837200
PMCPMC8035198

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.