Evidence map›Paper›PMID 20848086›Full record

ArticlePsychopharmacology2011

Effect of the adenosine A2A receptor antagonist MSX-3 on motivational disruptions of maternal behavior induced by dopamine antagonism in the early postpartum rat.

Mariana Pereira, Andrew M Farrar, Jörg Hockemeyer, Christa E Müller, John D Salamone, Joan I Morrell

Abstract read
In one paragraph

Article in Psychopharmacology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  5. Oxytocin interactions with central dopamine and serotonin systems regulate different components of motherhood.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    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

6 authors at 3 institutions in 2 countries.

Mariana PereiraCenter for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, 197 University Avenue, Newark, NJ 07102, USA. pereiram@andromeda.rutgers.edu
Andrew M Farrar
Jörg Hockemeyer
Christa E Müller
John D Salamone
Joan I Morrell
Rutgers, The State University of New Jersey · USUniversity of Bonn · DEUniversity of Connecticut · US

Funding

Maternal Rat Preferences for Pups Versus CocaineR01DA014025 · NIDA · RUTGERS THE STATE UNIV OF NJ NEWARK · PI MORRELL, JOAN IRENE · 2003 to 2010
$1.2M
Effort-related Functions of Nucleus Accumbens Adenosine A2A ReceptorsR01MH078023 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI SALAMONE, JOHN D · 2007 to 2010
$835k
Cocaine disruption of maternal motivation: preference for pups vs. cocaineR03DA027945 · NIDA · RUTGERS THE STATE UNIV OF NJ NEWARK · PI PEREIRA ARBOLEYA, MARIANA · 2009 to 2010
$77k
NIDA NIH HHS DA014025NIDA NIH HHS DA027945NIDA NIH HHS R01 DA014025NIDA NIH HHS R03 DA027945NIMH NIH HHS MH078023NIMH NIH HHS R01 MH078023
6 · The paper itself

Abstract

rationaleMesolimbic dopamine (DA), particularly in the nucleus accumbens, importantly regulates activational aspects of maternal responsiveness. DA antagonism and accumbens DA depletions interfere with early postpartum maternal motivation by selectively affecting most forms of active maternal behaviors, while leaving nursing behavior relatively intact. Considerable evidence indicates that there is a functional interaction between DA D2 and adenosine A(2A) receptors in striatal areas, including the nucleus accumbens.

objectiveThis study was conducted to determine if adenosine A(2A) receptor antagonism could reverse the effects of DA receptor antagonism on early postpartum maternal behavior.

methodsThe adenosine A(2A) receptor antagonist MSX-3 (0.25-2.0 mg/kg, IP) was investigated for its ability to reverse the effects of the DA D2 receptor antagonist haloperidol (0.1 mg/kg, IP) on the maternal behavior of early postpartum female rats.

resultsHaloperidol severely impaired the expression of active maternal components, including retrieval and grouping the pups at the nest site, pup licking, and nest building. Co-administration of MSX-3 (0.25-2.0 mg/kg, IP) with haloperidol produced a dose-related attenuation of the haloperidol-induced behavioral deficits in early postpartum females. Doses of MSX-3 that effectively reversed the effects of haloperidol (0.5, 1.0 mg/kg), when administered in the absence of haloperidol, did not affect maternal responding or locomotor activity.

conclusionsAdenosine and DA systems interact to regulate early postpartum maternal responsiveness. This research may potentially contribute to the development of strategies for treatments of psychiatric disorders during the postpartum period, with particular emphasis in maintaining or restoring the mother-infant relationship.

Indexed as

AnimalsDopamine AntagonistsDose-Response Relationship, DrugDrug InteractionsFemaleHaloperidolMaternal BehaviorMotor ActivityPostpartum PeriodPurinergic P1 Receptor AntagonistsRatsRats, Sprague-DawleyXanthinesDopamine AntagonistsHaloperidolMSX 3 compoundPurinergic P1 Receptor AntagonistsXanthines

Identifiers

PMID20848086
PMCPMC3077895
OpenAlexW2103833972

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.