Microstimulation of the Human Substantia Nigra Alters Reinforcement Learning
Animal studies have shown that substantia nigra (SN) dopaminergic (DA) neurons strengthen action–reward associations during reinforcement learning, but their role in human learning is not known. Here, we applied microstimulation in the SN of 11 patients undergoing deep brain stimulation surgery for...
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Published in | The Journal of neuroscience Vol. 34; no. 20; pp. 6887 - 6895 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Neuroscience
14.05.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Animal studies have shown that substantia nigra (SN) dopaminergic (DA) neurons strengthen action–reward associations during reinforcement learning, but their role in human learning is not known. Here, we applied microstimulation in the SN of 11 patients undergoing deep brain stimulation surgery for the treatment of Parkinson's disease as they performed a two-alternative probability learning task in which rewards were contingent on stimuli, rather than actions. Subjects demonstrated decreased learning from reward trials that were accompanied by phasic SN microstimulation compared with reward trials without stimulation. Subjects who showed large decreases in learning also showed an increased bias toward repeating actions after stimulation trials; therefore, stimulation may have decreased learning by strengthening action–reward associations rather than stimulus–reward associations. Our findings build on previous studies implicating SN DA neurons in preferentially strengthening action–reward associations during reinforcement learning. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: A.G.R., G.H.B., and M.J.K. designed research; A.G.R. and G.H.B. performed research; A.M. contributed unpublished reagents/analytic tools; A.G.R. analyzed data; A.G.R. and M.J.K. wrote the paper. G.H.B. and M.J.K. contributed equally to this work. |
ISSN: | 0270-6474 1529-2401 1529-2401 |
DOI: | 10.1523/JNEUROSCI.5445-13.2014 |