Evidence map›Paper›PMID 27974615›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Interaction of Instrumental and Goal-Directed Learning Modulates Prediction Error Representations in the Ventral Striatum.

Rong Guo, Wendelin Böhmer, Martin Hebart, Samson Chien, Tobias Sommer, Klaus Obermayer, Jan Gläscher

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  5. Executive Function Assigns Value to Novel Goal-Congruent Outcomes.Cerebral cortex (New York, N.Y. : 1991) · 2021
    Article
  6. 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

7 authors at 4 institutions in 2 countries.

Rong GuoInstitute of Software Engineering and Theoretical Computer Science, Technische Universität Berlin, Berlin 10587, Germany, rong@ni.tu-berlin.de.
Wendelin BöhmerInstitute of Software Engineering and Theoretical Computer Science, Technische Universität Berlin, Berlin 10587, Germany.
Martin HebartInstitute for Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg 20246, Germany, and.ORCID 0000-0001-7257-428X
Samson ChienInstitute for Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg 20246, Germany, and.
Tobias SommerInstitute for Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg 20246, Germany, and.
Klaus ObermayerInstitute of Software Engineering and Theoretical Computer Science, Technische Universität Berlin, Berlin 10587, Germany.
Jan GläscherInstitute for Systems Neuroscience, University Medical Center Hamburg-Eppendorf, Hamburg 20246, Germany, and.ORCID 0000-0002-1020-7115
Universität Hamburg · DEBernstein Center for Computational Neuroscience Berlin · DENorthwestern Polytechnical University · CNTechnische Universität Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Goal-directed and instrumental learning are both important controllers of human behavior. Learning about which stimulus event occurs in the environment and the reward associated with them allows humans to seek out the most valuable stimulus and move through the environment in a goal-directed manner. Stimulus-response associations are characteristic of instrumental learning, whereas response-outcome associations are the hallmark of goal-directed learning. Here we provide behavioral, computational, and neuroimaging results from a novel task in which stimulus-response and response-outcome associations are learned simultaneously but dominate behavior at different stages of the experiment. We found that prediction error representations in the ventral striatum depend on which type of learning dominates. Furthermore, the amygdala tracks the time-dependent weighting of stimulus-response versus response-outcome learning. Our findings suggest that the goal-directed and instrumental controllers dynamically engage the ventral striatum in representing prediction errors whenever one of them is dominating choice behavior. SIGNIFICANCE STATEMENT: Converging evidence in human neuroimaging studies has shown that the reward prediction errors are correlated with activity in the ventral striatum. Our results demonstrate that this region is simultaneously correlated with a stimulus prediction error. Furthermore, the learning system that is currently dominating behavioral choice dynamically engages the ventral striatum for computing its prediction errors. This demonstrates that the prediction error representations are highly dynamic and influenced by various experimental context. This finding points to a general role of the ventral striatum in detecting expectancy violations and encoding error signals regardless of the specific nature of the reinforcer itself.

Indexed as

GoalsAdultAlgorithmsAmygdalaConditioning, OperantFemaleHumansImage Processing, Computer-AssistedLearningMagnetic Resonance ImagingMaleModels, NeurologicalNeuroimagingPsychomotor PerformanceRewardVentral Striatumamygdalagoal-directed learningprediction errorventral striatum

Identifiers

PMID27974615
PMCPMC6705659
OpenAlexW2564900578

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.