Evidence map›Paper›PMID 23346966›Full record

ArticleAddiction biology2014

Opioid system in the medial prefrontal cortex mediates binge-like eating.

Angelo Blasio, Luca Steardo, Valentina Sabino, Pietro Cottone

Abstract read
In one paragraph

Article in Addiction biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
11.0field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 89 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

4 authors at 2 institutions in 2 countries.

Angelo BlasioLaboratory of Addictive Disorders, Departments of Pharmacology and Psychiatry, Boston University School of Medicine, Boston, MA, USA.
Luca Steardo
Valentina Sabino
Pietro Cottone
Boston University · USSapienza University of Rome · IT

Funding

Role of Neuropeptides in AnxietyR01MH093650 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SABINO, VALENTINA · 2012 to 2016
$2.0M
Role of the Endocannabinoid System in Compulsive EatingR01MH091945 · NIMH · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COTTONE, PIETRO · 2010 to 2014
$2.0M
Neurobiology of compulsive eating.R01DA030425 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COTTONE, PIETRO · 2011 to 2015
$1.6M
The dark side of preferred food addiction: role of CRF systemsR00DA023680 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI COTTONE, PIETRO · 2009 to 2011
$735k
Role of sigma receptors in ethanol reinforcementR00AA016731 · NIAAA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SABINO, VALENTINA · 2009 to 2011
$732k
The dark side of preferred food addiction: role of CRF systemsK99DA023680 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI COTTONE, PIETRO · 2007 to 2008
$179k
Role of sigma receptors in ethanol reinforcementK99AA016731 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI SABINO, VALENTINA · 2007 to 2008
$153k
NIAAA NIH HHS AA016731NIAAA NIH HHS K99 AA016731NIAAA NIH HHS R00 AA016731NIDA NIH HHS DA023680NIDA NIH HHS DA030425NIDA NIH HHS K99 DA023680NIDA NIH HHS R00 DA023680NIDA NIH HHS R01 DA030425NIMH NIH HHS MH091945NIMH NIH HHS MH093650A1NIMH NIH HHS R01 MH091945NIMH NIH HHS R01 MH093650
6 · The paper itself

Abstract

Binge eating disorder is an addiction-like disorder characterized by excessive food consumption within discrete periods of time. This study was aimed at understanding the role of the opioid system within the medial prefrontal cortex (mPFC) in the consummatory and motivational aspects of binge-like eating. For this purpose, we trained male rats to obtain either a sugary, highly palatable diet (Palatable rats) or a chow diet (Chow rats) for 1 hour/day. We then evaluated the effects of the opioid receptor antagonist, naltrexone, given either systemically or site-specifically into the nucleus accumbens (NAcc) or the mPFC on a fixed ratio 1 (FR1) and a progressive ratio schedule of reinforcement for food. Finally, we assessed the expression of the genes proopiomelanocortin (POMC), pro-dynorphin (PDyn) and pro-enkephalin (PEnk), coding for the opioids peptides in the NAcc and the mPFC in both groups. Palatable rats rapidly escalated their intake by four times. Naltrexone, when administered systemically and into the NAcc, reduced FR1 responding for food and motivation to eat under a progressive ratio in both Chow and Palatable rats; conversely, when administered into the mPFC, the effects were highly selective for binge eating rats. Furthermore, we found a twofold increase in POMC and a ∼50% reduction in PDyn gene expression in the mPFC of Palatable rats, when compared to control rats; however, no changes were observed in the NAcc. Our data suggest that neuroadaptations of the opioid system in the mPFC occur following intermittent access to highly palatable food, which may be responsible for the development of binge-like eating.

Indexed as

Analysis of VarianceAnimalsBinge-Eating DisorderConditioning, OperantDisease Models, AnimalFeeding BehaviorMaleMotivationNaltrexoneNarcotic AntagonistsOpioid PeptidesPrefrontal CortexRatsRats, WistarReinforcement, PsychologyNaltrexoneNarcotic AntagonistsOpioid PeptidesAddictionbinge eating disordernucleus accumbensopioidpalatabilityprefrontal cortex

Identifiers

PMID23346966
PMCPMC3664255
OpenAlexW1578443733

What OpenQuestion holds

Textmetadata
LicenceTDM
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.