Evidence map›Paper›PMID 26234587›Full record

ArticleNeurobiology of learning and memory2015

Extinction learning is slower, weaker and less context specific after alcohol.

James A Bisby, John A King, Valentina Sulpizio, Fanny Degeilh, H Valerie Curran, Neil Burgess

Open access · hybridAbstract read
In one paragraph

Article in Neurobiology of learning and memory, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 37% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

6 authors at 4 institutions in 3 countries.

James A BisbyInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, London, WC1N 3AR, UK; Institute of Neurology, University College London, Queen Square, London, WC1 3BG, UK. Electronic address: j.bisby@ucl.ac.uk.
John A KingInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, London, WC1N 3AR, UK; Clinical, Education and Health Psychology, University College London, London, UK.
Valentina SulpizioDepartment of Psychology, Sapienza University, Rome, Italy; Laboratory of Neuropsychology, Fondazione Santa Lucia IRCCS, Roma, Italy.
Fanny DegeilhInserm-EPHE-UCBN, Unité U1077, Boulevard Becquerel, 14000 Caen, France.
H Valerie CurranClinical Psychopharmacology Unit, University College London, London, UK; Clinical, Education and Health Psychology, University College London, London, UK.
Neil BurgessInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, London, WC1N 3AR, UK; Institute of Neurology, University College London, Queen Square, London, WC1 3BG, UK. Electronic address: n.burgess@ucl.ac.uk.
University College London · GBInserm · FRNational Hospital for Neurology and Neurosurgery · GBSapienza University of Rome · IT

Funding

Medical Research Council G1000854Wellcome Trust 091593Wellcome Trust 095811
6 · The paper itself

Abstract

Alcohol is frequently involved in psychological trauma and often used by individuals to reduce fear and anxiety. We examined the effects of alcohol on fear acquisition and extinction within a virtual environment. Healthy volunteers were administered alcohol (0.4g/kg) or placebo and underwent acquisition and extinction from different viewpoints of a virtual courtyard, in which the conditioned stimulus, paired with a mild electric shock, was centrally located. Participants returned the following day to test fear recall from both viewpoints of the courtyard. Skin conductance responses were recorded as an index of conditioned fear. Successful fear acquisition under alcohol contrasted with impaired extinction learning evidenced by persistent conditioned responses (Experiment 1). Participants' impairments in extinction under alcohol correlated with impairments in remembering object-locations in the courtyard seen from one viewpoint when tested from the other viewpoint. Alcohol-induced extinction impairments were overcome by increasing the number of extinction trials (Experiment 2). However, a test of fear recall the next day showed persistent fear in the alcohol group across both viewpoints. Thus, alcohol impaired extinction rather than acquisition of fear, suggesting that extinction is more dependent than acquisition on alcohol-sensitive representations of spatial context. Overall, extinction learning under alcohol was slower, weaker and less context-specific, resulting in persistent fear at test that generalized to the extinction viewpoint. The selective effect on extinction suggests an effect of alcohol on prefrontal involvement, while the reduced context-specificity implicates the hippocampus. These findings have important implications for the use of alcohol by individuals with clinical anxiety disorders.

Indexed as

AdolescentAdultConditioning, ClassicalElectric StimulationEthanolExtinction, PsychologicalFearFemaleHumansLearningMaleMental RecallYoung AdultEthanolAlcoholExtinctionFear memory

Identifiers

PMID26234587
PMCPMC4655873
OpenAlexW999834833

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.