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Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation

Prolonged mesolimbic dopamine concentration changes have been detected during spatial navigation, but little is known about the conditions that engender this signaling profile or how it develops with learning. To address this, we monitored dopamine concentration changes in the nucleus accumbens core...

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Autores principales: Collins, Anne L., Greenfield, Venuz Y., Bye, Jeffrey K., Linker, Kay E., Wang, Alice S., Wassum, Kate M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751524/
https://www.ncbi.nlm.nih.gov/pubmed/26869075
http://dx.doi.org/10.1038/srep20231
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author Collins, Anne L.
Greenfield, Venuz Y.
Bye, Jeffrey K.
Linker, Kay E.
Wang, Alice S.
Wassum, Kate M.
author_facet Collins, Anne L.
Greenfield, Venuz Y.
Bye, Jeffrey K.
Linker, Kay E.
Wang, Alice S.
Wassum, Kate M.
author_sort Collins, Anne L.
collection PubMed
description Prolonged mesolimbic dopamine concentration changes have been detected during spatial navigation, but little is known about the conditions that engender this signaling profile or how it develops with learning. To address this, we monitored dopamine concentration changes in the nucleus accumbens core of rats throughout acquisition and performance of an instrumental action sequence task. Prolonged dopamine concentration changes were detected that ramped up as rats executed each action sequence and declined after earned reward collection. With learning, dopamine concentration began to rise increasingly earlier in the execution of the sequence and ultimately backpropagated away from stereotyped sequence actions, becoming only transiently elevated by the most distal and unexpected reward predictor. Action sequence-related dopamine signaling was reactivated in well-trained rats if they became disengaged in the task and in response to an unexpected change in the value, but not identity of the earned reward. Throughout training and test, dopamine signaling correlated with sequence performance. These results suggest that action sequences can engender a prolonged mode of dopamine signaling in the nucleus accumbens core and that such signaling relates to elements of the motivation underlying sequence execution and is dynamic with learning, overtraining and violations in reward expectation.
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spelling pubmed-47515242016-02-22 Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation Collins, Anne L. Greenfield, Venuz Y. Bye, Jeffrey K. Linker, Kay E. Wang, Alice S. Wassum, Kate M. Sci Rep Article Prolonged mesolimbic dopamine concentration changes have been detected during spatial navigation, but little is known about the conditions that engender this signaling profile or how it develops with learning. To address this, we monitored dopamine concentration changes in the nucleus accumbens core of rats throughout acquisition and performance of an instrumental action sequence task. Prolonged dopamine concentration changes were detected that ramped up as rats executed each action sequence and declined after earned reward collection. With learning, dopamine concentration began to rise increasingly earlier in the execution of the sequence and ultimately backpropagated away from stereotyped sequence actions, becoming only transiently elevated by the most distal and unexpected reward predictor. Action sequence-related dopamine signaling was reactivated in well-trained rats if they became disengaged in the task and in response to an unexpected change in the value, but not identity of the earned reward. Throughout training and test, dopamine signaling correlated with sequence performance. These results suggest that action sequences can engender a prolonged mode of dopamine signaling in the nucleus accumbens core and that such signaling relates to elements of the motivation underlying sequence execution and is dynamic with learning, overtraining and violations in reward expectation. Nature Publishing Group 2016-02-12 /pmc/articles/PMC4751524/ /pubmed/26869075 http://dx.doi.org/10.1038/srep20231 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Collins, Anne L.
Greenfield, Venuz Y.
Bye, Jeffrey K.
Linker, Kay E.
Wang, Alice S.
Wassum, Kate M.
Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title_full Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title_fullStr Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title_full_unstemmed Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title_short Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
title_sort dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751524/
https://www.ncbi.nlm.nih.gov/pubmed/26869075
http://dx.doi.org/10.1038/srep20231
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