Evidence map›Paper›PMID 22176724›Full record

ArticleThe international journal of neuropsychopharmacology2012

Dopamine D1 receptor involvement in latent inhibition and overshadowing.

Andrew J D Nelson, Karen E Thur, Helen J Cassaday

Open access · hybridAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 38% 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, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Scopolamine Impairs Appetitive But Not Aversive Trace Conditioning: Role of the Medial Prefrontal Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  5. Article
  6. Phasic dopamine release in the medial prefrontal cortex enhances stimulus discrimination.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  7. Article
  8. Dopamine D1 receptor stimulation modulates the formation and retrieval of novel object recognition memory: Role of the prelimbic cortex.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2015
    Article
  9. Article
  10. Article
  11. Review
  12. D-amphetamine and antipsychotic drug effects on latent inhibition in mice lacking dopamine D2 receptors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Article
  13. Article
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

3 authors at 1 institution in 1 country.

Andrew J D NelsonSchool of Psychology, University of Nottingham, University Park, Nottingham, UK.
Karen E Thur
Helen J Cassaday
University of Nottingham · GB

Funding

Wellcome Trust 082940
6 · The paper itself

Abstract

Latent inhibition (LI) manifests as poorer conditioning to a stimulus that has previously been experienced without consequence. There is good evidence of dopaminergic modulation of LI, as the effect is reliably disrupted by the indirect dopamine (DA) agonist amphetamine. The disruptive effects of amphetamine on LI are reversed by both typical and atypical antipsychotics, which on their own are able to facilitate LI. However, the contribution of different DA receptors to these effects is poorly understood. Amphetamine effects on another stimulus selection procedure, overshadowing, have been suggested to be D1-mediated. Thus, in the current experiments, we systematically investigated the role of D1 receptors in LI. First, we tested the ability of the full D1 agonist SKF 81297 to abolish LI and compared the effects of this drug on LI and overshadowing. Subsequently, we examined whether the D1 antagonist SCH 23390 can lead to the emergence of LI under conditions that do not produce the effect in normal animals (weak pre-exposure). Finally, we tested the ability of SCH 23390 to block amphetamine-induced disruption of LI. We found little evidence that direct stimulation of D1 receptors abolishes LI (although there was some attenuation of LI at 0.4 mg/kg SKF 81297). Similarly, SCH 23390 failed to enhance LI. However, SCH 23390 did block amphetamine-induced disruption of LI. These data indicate that, while LI may be unaffected by selective manipulation of activity at D1 receptors, the effects of amphetamine on LI are to some extent dependent on actions at D1 receptors.

Indexed as

Inhibition, PsychologicalAmphetamineAnimalsBenzazepinesConditioning, PsychologicalDopamine AntagonistsDose-Response Relationship, DrugMaleRatsRats, WistarReaction TimeReceptors, Dopamine D1AmphetamineBenzazepinesDopamine AntagonistsReceptors, Dopamine D1SCH 23390

Identifiers

PMID22176724
PMCPMC3496172
OpenAlexW2136393682

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.