Evidence map›Paper›PMID 18649072›Full record

Trial reportPsychopharmacology2008

Pharmacological modulation of the neural basis underlying inhibition of return (IOR) in the human 5-HT2A agonist and NMDA antagonist model of psychosis.

Jörg Daumann, Karsten Heekeren, Anna Neukirch, Christiane M Thiel, Walter Möller-Hartmann, Euphrosyne Gouzoulis-Mayfrank

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Psychopharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
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  5. Effects of ketamine-induced psychopathological symptoms on continuous overt rhyme fluency.European archives of psychiatry and clinical neuroscience · 2012
    Trial
  6. Psilocybin-induced deficits in automatic and controlled inhibition are attenuated by ketanserin in healthy human volunteers.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Trial
  7. Review
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  12. Review
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  15. Review
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  18. Article
  19. Neuropharmacology of N,N-dimethyltryptamine.Brain research bulletin · 2016
    Review
  20. Clinical applications of hallucinogens: A review.Experimental and clinical psychopharmacology · 2016
    Review
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 2 institutions in 1 country.

Jörg DaumannDepartment of Psychiatry and Psychotherapy, University of Cologne, Kerpener Strasse 62, 50924 Cologne, Germany. joerg.daumann@uk-koeln.de
Karsten Heekeren
Anna Neukirch
Christiane M Thiel
Walter Möller-Hartmann
Euphrosyne Gouzoulis-Mayfrank
University of Cologne · DEErnst Ruska Centre · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleAttentional deficits are common symptoms in schizophrenia. Recent evidence suggests that schizophrenic patients show abnormalities in spatial orienting of attention, particularly a deficit of inhibition of return (IOR). IOR is mostly thought to reflect an automatic, inhibitory mechanism protecting the organism from redirecting attention to previously scanned, insignificant locations. Pharmacologic challenges with hallucinogens have been used as models for psychosis.

objectivesThe aim of this study was to investigate the neural correlates underlying orienting of attention in the human N-methyl-D-aspartic acid antagonist and 5-HT2A agonist models of psychosis. MATERIALS AND

methodsFourteen healthy volunteers participated in a randomized, double-blind, cross-over event-related functional magnetic resonance imaging (fMRI) study with dimethyltryptamine (DMT) and S-ketamine. We administered a covert orienting of attention task with nonpredictive peripheral cues, and we scanned the subjects on two separate days at least 14 days apart with a placebo and a verum condition on each day.

resultsDMT, but not S-ketamine, slowed down reaction times significantly. IOR was blunted after DMT, but not after S-ketamine. Relative to placebo, S-ketamine increased activation in the IOR condition in the right superior frontal gyrus, left superior temporal gyrus, and right midfrontal frontal gyrus.

conclusionsThe discrepancy between the behavioral and functional imaging outcome indicates that pharmacological fMRI might be a sensitive tool to detect drug-modulated blood oxygenation level-dependent signal changes in the absence of behavioral abnormalities. Our findings might help to further clarify the contradictory findings of IOR in schizophrenic patients and might, thus, shed more light on possible differential pathomechanisms of schizophrenic symptoms.

Indexed as

Inhibition, PsychologicalSerotonin 5-HT2 Receptor AgonistsAdultAttentionCross-Over StudiesCuesDouble-Blind MethodFemaleHumansKetamineMagnetic Resonance ImagingMaleModels, BiologicalN,N-DimethyltryptaminePsychoses, Substance-InducedReaction TimeKetamineN,N-DimethyltryptamineReceptors, N-Methyl-D-AspartateSerotonin 5-HT2 Receptor Agonists

Identifiers

PMID18649072
OpenAlexW2023839383

What OpenQuestion holds

Textmetadata
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.