Evidence map›Paper›PMID 19132351›Full record

ArticlePsychopharmacology2009

The adenosine A2A antagonist MSX-3 reverses the effects of the dopamine antagonist haloperidol on effort-related decision making in a T-maze cost/benefit procedure.

Allison M Mott, Eric J Nunes, Lyndsey E Collins, Russell G Port, Kelly S Sink, Jörg Hockemeyer, Christa E Müller, John D Salamone

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
6.3field-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

52 citing papers in PubMed, 114 citations in OpenAlex.

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  10. Vigor, Effort-Related Aspects of Motivation and Anhedonia.Current topics in behavioral neurosciences · 2022
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  14. Inhibition of Catechol-Frontiers in behavioral neuroscience · 2020
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  15. Blockade of muscarinic acetylcholine receptors facilitates motivated behaviour and rescues a model of antipsychotic-induced amotivation.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Article
  16. 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 2 countries.

Allison M MottDepartment of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.
Eric J Nunes
Lyndsey E Collins
Russell G Port
Kelly S Sink
Jörg Hockemeyer
Christa E Müller
John D Salamone
University of Connecticut · USUniversity of Bonn · DE

Funding

Effort-related Functions of Nucleus Accumbens Adenosine A2A ReceptorsR01MH078023 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI SALAMONE, JOHN D · 2007 to 2010
$835k
NIMH NIH HHS MH078023NIMH NIH HHS R01 MH078023
6 · The paper itself

Abstract

rationaleMesolimbic dopamine (DA) is a critical component of the brain circuitry regulating behavioral activation and effort-related processes. Research involving choice tasks has shown that rats with impaired DA transmission reallocate their instrumental behavior away from food-reinforced tasks with high response requirements and instead select less effortful food-seeking behaviors.

objectivePrevious work showed that adenosine A(2A) antagonism can reverse the effects of the DA antagonist haloperidol in an operant task that assesses effort-related choice. The present work used a T-maze choice procedure to assess the effects of adenosine A(2A) and A(1) antagonism. MATERIALS AND

methodsWith this task, the two arms of the maze have different reinforcement densities (four vs. two food pellets), and a vertical 44 cm barrier is positioned in the arm with the higher density, presenting the animal with an effort-related challenge. Untreated rats strongly prefer the arm with the high density of food reward and climb the barrier in order to obtain the food.

resultsHaloperidol produced a dose-related (0.05-0.15 mg/kg i.p.) reduction in the number of trials in which the rats chose the high-barrier arm. Co-administration of the adenosine A(2A) receptor antagonist MSX-3 (0.75, 1.5, and 3.0 mg/kg i.p.), but not the A(1) antagonist 8-cyclopentyl-1,3-dipropylxanthine (0.75, 1.5, and 3.0 mg/kg i.p.), reversed the effects of haloperidol on effort-related choice and latency.

conclusionsAdenosine A(2A) and D2 receptors interact to regulate effort-related decision making, which may have implications for the treatment of psychiatric symptoms such as psychomotor slowing or anergia that can be observed in depression, parkinsonism, and other disorders.

Indexed as

Adenosine A2 Receptor AntagonistsAdenosine A1 Receptor AntagonistsAnimalsBehavior, AnimalChoice BehaviorConditioning, OperantDopamine AntagonistsDose-Response Relationship, DrugDrug InteractionsHaloperidolMaleMaze LearningMotivationNucleus AccumbensPhysical ExertionPsychomotor Performance1,3-dipropyl-8-cyclopentylxanthineAdenosine A1 Receptor AntagonistsAdenosine A2 Receptor AntagonistsDopamine AntagonistsHaloperidolMSX 3 compoundReceptor, Adenosine A1Receptors, Adenosine A2Xanthines

Identifiers

PMID19132351
PMCPMC2875244
OpenAlexW1965354593

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.