Evidence map›Paper›PMID 23474592›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2013

Amylin receptor signaling in the ventral tegmental area is physiologically relevant for the control of food intake.

Elizabeth G Mietlicki-Baase, Laura E Rupprecht, Diana R Olivos, Derek J Zimmer, Mark D Alter, R Christopher Pierce, Heath D Schmidt, Matthew R Hayes

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 94 citations in OpenAlex.

  1. Amylin: A Multi-Functional Pancreatic Hormone-A Review.Diabetes, obesity & metabolism · 2026
    Review
  2. Article
  3. Brain Amylin Signaling, Feeding, and Reward.Comprehensive Physiology · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
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  13. Article
  14. Article
  15. Review
  16. Calcitonin receptor signaling in nucleus accumbens D1R- and D2R-expressing medium spiny neurons bidirectionally alters opioid taking in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  17. Review
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  19. Article
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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

8 authors at 2 institutions in 1 country.

Elizabeth G Mietlicki-BaaseTranslational Neuroscience Program, Department of Psychiatry, Perelman School of Medicine at University of Pennsylvania, Philadelphia, PA 19104, USA. ebaase@mail.med.upenn.edu
Laura E Rupprecht
Diana R Olivos
Derek J Zimmer
Mark D Alter
R Christopher Pierce
Heath D Schmidt
Matthew R Hayes
University of Pennsylvania · USTranslational Therapeutics (United States) · US

Funding

VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI DOUGLAS J EPSTEIN · 1986 to 2026
$48.3M
D1 Dopamine Receptor Signaling and Cocaine ReinstatementR01DA022339 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI PIERCE, ROBERT CHRISTOPHER · 2008 to 2012
$1.8M
Neuroendocrinology of Energy Balance ControlR01DK096139 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HAYES, MATTHEW R · 2012 to 2016
$1.7M
Psychostimulant-Induced Craving and ToxicityK02DA018678 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI PIERCE, ROBERT CHRISTOPHER · 2006 to 2015
$1.2M
Epigenetics and Incubation of CravingK01DA030445 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI SCHMIDT, HEATH D · 2010 to 2014
$668k
Neuroendocrinology of energy balance control: role of glucagon-like-peptide-1K01DK085435 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HAYES, MATTHEW R · 2010 to 2012
$396k
Neural mechanism of glucagon-like-peptide-1 receptor-mediated nausea /malaiseR03DK093874 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HAYES, MATTHEW R · 2012 to 2013
$157k
NIDA NIH HHS DA030445NIDA NIH HHS DA18678NIDA NIH HHS DA22339NIDA NIH HHS K01 DA030445NIDA NIH HHS K02 DA018678NIDA NIH HHS R01 DA022339NIDDK NIH HHS DK085435NIDDK NIH HHS DK093874NIDDK NIH HHS DK096139NIDDK NIH HHS DK19525NIDDK NIH HHS K01 DK085435NIDDK NIH HHS P30 DK019525NIDDK NIH HHS R01 DK096139NIDDK NIH HHS R03 DK093874
6 · The paper itself

Abstract

The ability of amylin, a pancreatic β-cell-derived neuropeptide, to promote negative energy balance has been ascribed to neural activation at the area postrema. However, despite amylin binding throughout the brain, the possible role of amylin signaling at other nuclei in the control of food intake has been largely neglected. We show that mRNA for all components of the amylin receptor complex is expressed in the ventral tegmental area (VTA), a mesolimbic structure mediating food intake and reward. Direct activation of VTA amylin receptors reduces the intake of chow and palatable sucrose solution in rats. This effect is mediated by reductions in meal size and is not due to nausea/malaise or prolonged suppression of locomotor activity. VTA amylin receptor activation also reduces sucrose self-administration on a progressive ratio schedule. Finally, antagonist studies provide novel evidence that VTA amylin receptor blockade increases food intake and attenuates the intake-suppressive effects of a peripherally administered amylin analog, suggesting that amylin receptor signaling in the VTA is physiologically relevant for food intake control and potentially clinically relevant for the treatment of obesity.

Indexed as

Amylin Receptor AgonistsAnimalsCalcitoninDose-Response Relationship, DrugDrug InteractionsEatingMaleMicroinjectionsMotor ActivityNauseaPeptide FragmentsRatsReceptors, Islet Amyloid PolypeptideReinforcement ScheduleRewardRNA, MessengerAC 187Amylin Receptor AgonistsCalcitoninPeptide FragmentsReceptors, Islet Amyloid PolypeptideRNA, Messengersalmon calcitoninSucrose

Identifiers

PMID23474592
PMCPMC3717548
OpenAlexW2074458173

What OpenQuestion holds

Textmetadata
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.