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|a Atallah, Hisham E.
|e author
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|a Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
|e contributor
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|a McGovern Institute for Brain Research at MIT
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|a Atallah, Hisham E.
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|a McCool, Andrew D.
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|a Howe, Mark W.
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|a Graybiel, Ann M.
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|a McCool, Andrew D.
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|a Howe, Mark W.
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|a Graybiel, Ann M.
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|a Atallah, Hisham E.
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|a McCool, Andrew D.
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|a Howe, Mark W.
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|a Graybiel, Ann M.
|e author
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|a Neurons in the Ventral Striatum Exhibit Cell-Type-Specific Representations of Outcome during Learning
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|b Elsevier,
|c 2016-05-09T14:09:18Z.
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|z Get fulltext
|u http://hdl.handle.net/1721.1/102425
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|a The ventromedial striatum (VMS) is a node in circuits underpinning both affect and reinforcement learning. The cellular bases of these functions and especially their potential linkages have been unclear. VMS cholinergic interneurons, however, have been singled out as being related both to affect and to reinforcement-based conditioning, raising the possibility that unique aspects of their signaling could account for these functions. Here we show that VMS tonically active neurons (TANs), including putative cholinergic interneurons, generate unique bidirectional outcome responses during reward-based learning, reporting both positive (reward) and negative (reward omission) outcomes when behavioral change is prompted by switches in reinforcement contingencies. VMS output neurons (SPNs), by contrast, are nearly insensitive to switches in reinforcement contingencies, gradually losing outcome signaling while maintaining responses at trial initiation and goal approach. Thus, TANs and SPNs in the VMS provide distinct signals optimized for different aspects of the learning process.
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|a National Institutes of Health (U.S.) (Grant R01 MH060379)
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|a United States. Office of Naval Research (Grant N00014-04-1-0208)
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|a European Union (Grant 021716)
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|a Cure Huntington's Disease Initiative, Inc. (Grant A-5552)
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|a Nancy Lurie Marks Family Foundation
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|a William N. & Bernice E. Bumpus Foundation (Grant RRDA Pilot: 2013.1)
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|a en_US
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|a Article
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|t Neuron
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