Evidence map›Paper›PMID 26900078›Full record

Trial reportPsychopharmacology2016

An investigation into aripiprazole's partial D₂ agonist effects within the dorsolateral prefrontal cortex during working memory in healthy volunteers.

Anna Murphy, Serdar Dursun, Shane McKie, Rebecca Elliott, John Francis William Deakin

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pramipexole modulates fronto-subthalamic pathway in sequential working memory.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
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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

5 authors at 2 institutions in 2 countries.

Anna MurphyNeuroscience and Psychiatry Unit, Institute of Brain, Behaviour and Mental Health, University of Manchester, G.708 Stopford Building, Manchester, M13 9PT, UK. anna.murphy@manchester.ac.uk.
Serdar DursunDepartment of Psychiatry, University of Alberta, Edmonton, Alberta, Canada.
Shane McKieNeuroscience and Psychiatry Unit, Institute of Brain, Behaviour and Mental Health, University of Manchester, G.708 Stopford Building, Manchester, M13 9PT, UK.
Rebecca ElliottNeuroscience and Psychiatry Unit, Institute of Brain, Behaviour and Mental Health, University of Manchester, G.708 Stopford Building, Manchester, M13 9PT, UK.
John Francis William DeakinNeuroscience and Psychiatry Unit, Institute of Brain, Behaviour and Mental Health, University of Manchester, G.708 Stopford Building, Manchester, M13 9PT, UK.
University of Manchester · GBUniversity of Alberta · CA

Funding

Medical Research Council G0300653
6 · The paper itself

Abstract

rationaleWorking memory impairments in schizophrenia have been attributed to dysfunction of the dorsolateral prefrontal cortex (DLPFC) which in turn may be due to low DLPFC dopamine innervation. Conventional antipsychotic drugs block DLPFC D2 receptors, and this may lead to further dysfunction and working memory impairments. Aripiprazole is a D2 receptor partial agonist hypothesised to enhance PFC dopamine functioning, possibly improving working memory.

objectivesWe probed the implications of the partial D2 receptor agonist actions of aripiprazole within the DLPFC during working memory. Investigations were carried out in healthy volunteers to eliminate confounds of illness or medication status. Aripiprazole's prefrontal actions were compared with the D2/5-HT2A blocker risperidone to separate aripiprazole's unique prefrontal D2 agonist actions from its serotinergic and striatal D2 actions that it shares with risperidone.

methodA double-blind, placebo-controlled, parallel design was implemented. Participants received a single dose of either 5 mg aripiprazole, 1 mg risperidone or placebo before performing the n-back task whilst undergoing fMRI scanning.

resultsCompared with placebo, the aripiprazole group demonstrated enhanced DLPFC activation associated with a trend for improved discriminability (d') and speeded reaction times. In contrast to aripiprazole's neural effects, the risperidone group demonstrated a trend for reduced DLPFC recruitment. Unexpectedly, the risperidone group demonstrated similar effects to aripiprazole on d' and additionally had reduced errors of commission compared with placebo.

conclusionAripiprazole has unique DLPFC actions attributed to its prefrontal D2 agonist action. Risperidone's serotinergic action that results in prefrontal dopamine release may have protected against any impairing effects of its prefrontal D2 blockade.

Indexed as

AdultAntipsychotic AgentsAripiprazoleCorpus StriatumDopamineDouble-Blind MethodHealthy VolunteersHumansMaleMemory, Short-TermPrefrontal CortexReceptors, Dopamine D2RisperidoneAntipsychotic AgentsAripiprazoleDopamineDRD2 protein, humanReceptors, Dopamine D2RisperidoneAntipsychoticAripiprazoleD2DopamineDorsolateral prefrontaln-BackPartial agonismRisperidoneWorking memory

Identifiers

PMID26900078
PMCPMC4819596
OpenAlexW2281590068

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.