Evidence map›Paper›PMID 19048234›Full record

ArticlePsychopharmacology2009

The adenosine A2A antagonist MSX-3 reverses the effort-related effects of dopamine blockade: differential interaction with D1 and D2 family antagonists.

Lila T Worden, Mona Shahriari, Andrew M Farrar, 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 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  9. Vigor, Effort-Related Aspects of Motivation and Anhedonia.Current topics in behavioral neurosciences · 2022
    Review
  10. Allosteric Interactions between Adenosine AInternational journal of molecular sciences · 2021
    Review
  11. International society of sports nutrition position stand: caffeine and exercise performance.Journal of the International Society of Sports Nutrition · 2021
    Review
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  13. Review
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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

7 authors at 3 institutions in 2 countries.

Lila T WordenDivision of Behavioral Neuroscience, Department of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.
Mona Shahriari
Andrew M Farrar
Kelly S Sink
Jörg Hockemeyer
Christa E Müller
John D Salamone
University of Connecticut · USUniversity of Bonn · DENational Institute on Drug Abuse · US

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

rationaleBrain dopamine (DA) participates in the modulation of instrumental behavior, including aspects of behavioral activation and effort-related choice behavior. Rats with impaired DA transmission reallocate their behavior away from food-seeking behaviors that have high response requirements, and instead select less effortful alternatives. Although accumbens DA is considered a critical component of the brain circuitry regulating effort-related choice behavior, emerging evidence demonstrates a role for adenosine A(2A) receptors.

objectiveAdenosine A(2A) receptor antagonism has been shown to reverse the effects of DA antagonism. The present experiments were conducted to determine if this effect was dependent upon the subtype of DA receptor that was antagonized to produce the changes in effort-related choice. MATERIALS AND

methodsThe adenosine A(2A) receptor antagonist MSX-3 (0.5-2.0 mg/kg IP) was assessed for its ability to reverse the effects of the D1 family antagonist SCH39166 (ecopipam; 0.2 mg/kg IP) and the D2 family antagonist eticlopride (0.08 mg/kg IP), using a concurrent lever pressing/chow feeding procedure.

resultsMSX-3 produced a substantial dose-related reversal of the effects of eticlopride on lever pressing and chow intake. At the highest dose of MSX-3, there was a complete reversal of the effects of eticlopride on lever pressing. In contrast, MSX-3 produced only a minimal attenuation of the effects of SCH39166, as measured by regression and effect size analyses.

conclusionsThe greater ability of MSX-3 to reverse the effects of D2 vs. D1 blockade may be related to the colocalization of D2 and adenosine A(2A) receptors on the same population of striatal neurons.

Indexed as

Adenosine A2 Receptor AntagonistsDopamine D2 Receptor AntagonistsAnimalsBrainConditioning, OperantDopamineDopamine AntagonistsDose-Response Relationship, DrugDrug InteractionsMaleRatsRats, Sprague-DawleyReceptors, Dopamine D1XanthinesAdenosine A2 Receptor AntagonistsDopamineDopamine AntagonistsDopamine D2 Receptor AntagonistsMSX 3 compoundReceptors, Dopamine D1Xanthines

Identifiers

PMID19048234
PMCPMC2875246
OpenAlexW2093679869

What OpenQuestion holds

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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.