Subliminal Instrumental Conditioning Demonstrated in the Human Brain
How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating the values of context-action associations in proportion to a reward prediction error. Previous evidence suggests that such computations are ex...
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Published in | Neuron (Cambridge, Mass.) Vol. 59; no. 4; pp. 561 - 567 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
28.08.2008
Elsevier Limited Cell Press |
Subjects | |
Online Access | Get full text |
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Abstract | How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating the values of context-action associations in proportion to a reward prediction error. Previous evidence suggests that such computations are expressed in the striatum and, as they are cognitively impenetrable, represent an unconscious learning mechanism. Here, we formally test this by studying instrumental conditioning in a situation where we masked contextual cues, such that they were not consciously perceived. Behavioral data showed that subjects nonetheless developed a significant propensity to choose cues associated with monetary rewards relative to punishments. Functional neuroimaging revealed that during conditioning cue values and prediction errors, generated from a computational model, both correlated with activity in ventral striatum. We conclude that, even without conscious processing of contextual cues, our brain can learn their reward value and use them to provide a bias on decision making. |
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AbstractList | How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating the values of context-action associations in proportion to a reward prediction error. Previous evidence suggests that such computations are expressed in the striatum and, as they are cognitively impenetrable, represent an unconscious learning mechanism. Here, we formally test this by studying instrumental conditioning in a situation where we masked contextual cues, such that they were not consciously perceived. Behavioral data showed that subjects nonetheless developed a significant propensity to choose cues associated with monetary rewards relative to punishments. Functional neuroimaging revealed that during conditioning cue values and prediction errors, generated from a computational model, both correlated with activity in ventral striatum. We conclude that, even without conscious processing of contextual cues, our brain can learn their reward value and use them to provide a bias on decision making. How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating the values of context-action associations in proportion to a reward prediction error. Previous evidence suggests that such computations are expressed in the striatum and, as they are cognitively impenetrable, represent an unconscious learning mechanism. Here, we formally test this by studying instrumental conditioning in a situation where we masked contextual cues, such that they were not consciously perceived. Behavioral data showed that subjects nonetheless developed a significant propensity to choose cues associated with monetary rewards relative to punishments. Functional neuroimaging revealed that during conditioning cue values and prediction errors, generated from a computational model, both correlated with activity in ventral striatum. We conclude that, even without conscious processing of contextual cues, our brain can learn their reward value and use them to provide a bias on decision making.How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating the values of context-action associations in proportion to a reward prediction error. Previous evidence suggests that such computations are expressed in the striatum and, as they are cognitively impenetrable, represent an unconscious learning mechanism. Here, we formally test this by studying instrumental conditioning in a situation where we masked contextual cues, such that they were not consciously perceived. Behavioral data showed that subjects nonetheless developed a significant propensity to choose cues associated with monetary rewards relative to punishments. Functional neuroimaging revealed that during conditioning cue values and prediction errors, generated from a computational model, both correlated with activity in ventral striatum. We conclude that, even without conscious processing of contextual cues, our brain can learn their reward value and use them to provide a bias on decision making. |
Author | Frith, Chris D. Daunizeau, Jean Petrovic, Predrag Pessiglione, Mathias Palminteri, Stefano Dolan, Raymond J. |
AuthorAffiliation | 1 Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK 2 Laboratoire INSERM U610, Centre de NeuroImagerie de Recherche (CENIR), Institut Fédératif de Recherche en Neurosciences, Hôpital Pitié-Salpêtrière, Université Pierre et Marie Curie (Paris 6), 47 Boulevard de l'Hôpital 75013 Paris, France |
AuthorAffiliation_xml | – name: 2 Laboratoire INSERM U610, Centre de NeuroImagerie de Recherche (CENIR), Institut Fédératif de Recherche en Neurosciences, Hôpital Pitié-Salpêtrière, Université Pierre et Marie Curie (Paris 6), 47 Boulevard de l'Hôpital 75013 Paris, France – name: 1 Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK |
Author_xml | – sequence: 1 givenname: Mathias surname: Pessiglione fullname: Pessiglione, Mathias email: mathias.pessiglione@gmail.com organization: Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK – sequence: 2 givenname: Predrag surname: Petrovic fullname: Petrovic, Predrag organization: Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK – sequence: 3 givenname: Jean surname: Daunizeau fullname: Daunizeau, Jean organization: Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK – sequence: 4 givenname: Stefano surname: Palminteri fullname: Palminteri, Stefano organization: Laboratoire INSERM U610, Centre de NeuroImagerie de Recherche (CENIR), Institut Fédératif de Recherche en Neurosciences, Hôpital Pitié-Salpêtrière, Université Pierre et Marie Curie (Paris 6), 47 Boulevard de l'Hôpital 75013 Paris, France – sequence: 5 givenname: Raymond J. surname: Dolan fullname: Dolan, Raymond J. organization: Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK – sequence: 6 givenname: Chris D. surname: Frith fullname: Frith, Chris D. organization: Wellcome Trust Centre for NeuroImaging, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18760693$$D View this record in MEDLINE/PubMed |
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Snippet | How the brain uses success and failure to optimize future decisions is a long-standing question in neuroscience. One computational solution involves updating... |
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Title | Subliminal Instrumental Conditioning Demonstrated in the Human Brain |
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