Evidence map›Paper›PMID 22579970›Full record

ArticleBehavioural brain research2012

Dopamine signaling in the medial prefrontal cortex and amygdala is required for the acquisition of fructose-conditioned flavor preferences in rats.

Danielle C Malkusz, Theodore Banakos, Andrew Mohamed, Tracy Vongwattanakit, Gina Malkusz, Shermeen Saeed, Stewart Martinez, Tara Bohn, Fizza Mahmud, Cami Liss and 4 more

Abstract read
In one paragraph

Article in Behavioural brain research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 35 citations in OpenAlex.

  1. Dissociable control of μ-opioid-driven hyperphagia vs. food impulsivity across subregions of medial prefrontal, orbitofrontal, and insular cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  2. The Role of Dorsal Hippocampal Dopamine D1-Type Receptors in Social Learning, Social Interactions, and Food Intake in Male and Female Mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    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

14 authors at 3 institutions in 1 country.

Danielle C MalkuszNeuropsychology Doctoral Subprogram, Graduate Center, City University of New York, New York, NY, USA.
Theodore Banakos
Andrew Mohamed
Tracy Vongwattanakit
Gina Malkusz
Shermeen Saeed
Stewart Martinez
Tara Bohn
Fizza Mahmud
Cami Liss
Abraham Rozvi
Khalid Touzani
Anthony Sclafani
Richard J Bodnar
Queens College, CUNY · USCity University of New York · USThe Graduate Center, CUNY · US

Funding

Neuropharmacology of Learned Food PreferencesR01DK071761 · NIDDK · BROOKLYN COLLEGE · PI SCLAFANI, ANTHONY · 2005 to 2009
$1.3M
NIDDK NIH HHS DK071761NIDDK NIH HHS R01 DK071761
6 · The paper itself

Abstract

Systemic administration of dopamine (DA) D1 (SCH23390: SCH) and D2 (raclopride: RAC) antagonists blocked both acquisition and expression of fructose-conditioned flavor preferences (CFP). It is unclear what brain circuits are involved in mediating these effects. The present study investigated DA signaling within the nucleus accumbens shell (NAcS), amygdala (AMY) and medial prefrontal cortex (mPFC) in the acquisition and expression of fructose-CFP. In Experiment 1, separate groups of rats were injected daily in the NAcS or AMY with saline, SCH (24 nmol) or RAC (24 nmol) prior to training sessions with a flavor (CS+) mixed with 8% fructose and 0.2% saccharin (CS+/F) and a different flavor (CS-) mixed with only 0.2% saccharin. In the two-bottle choice tests with 0.2% saccharin, only rats injected with RAC in the AMY failed to acquire a CS+ preference (45-54%). In Experiment 2, new rats were identically trained, but saline, SCH and RAC were injected in the mPFC. In subsequent two-bottle choice tests, SCH- and RAC-treated rats failed to exhibit a CS+ preference (50-56%). In Experiment 3, new rats were trained with CS+/F and CS- without injections. Subsequent two-bottle choice tests were then conducted following bilateral injections of SCH or RAC in the mPFC at total doses of 0, 12, 24 and 48 nmol. Expression of the CS+ preference failed to be affected by either antagonist, indicating that the mPFC is not involved in the maintenance of this preference. These data indicate that the acquisition of fructose-CFP is dependent on DA signaling in the mPFC and AMY.

Indexed as

AmygdalaAnalysis of VarianceAnimalsBenzazepinesConditioning, OperantDopamineDopamine AntagonistsDose-Response Relationship, DrugFood PreferencesFructoseMalePrefrontal CortexRacloprideRatsRats, Sprague-DawleyTime FactorsBenzazepinesDopamineDopamine AntagonistsFructoseRacloprideSCH 23390

Identifiers

PMID22579970
PMCPMC3741658
OpenAlexW1980877451

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.