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Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release

Recent computational models of sign tracking (ST) and goal tracking (GT) have accounted for observations that dopamine (DA) is not necessary for all forms of learning and have provided a set of predictions to further their validity. Among these, a central prediction is that manipulating the intertri...

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Autores principales: Lee, Brian, Gentry, Ronny N., Bissonette, Gregory B., Herman, Rae J., Mallon, John J., Bryden, Daniel W., Calu, Donna J., Schoenbaum, Geoffrey, Coutureau, Etienne, Marchand, Alain R., Khamassi, Mehdi, Roesch, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175531/
https://www.ncbi.nlm.nih.gov/pubmed/30256785
http://dx.doi.org/10.1371/journal.pbio.2004015
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author Lee, Brian
Gentry, Ronny N.
Bissonette, Gregory B.
Herman, Rae J.
Mallon, John J.
Bryden, Daniel W.
Calu, Donna J.
Schoenbaum, Geoffrey
Coutureau, Etienne
Marchand, Alain R.
Khamassi, Mehdi
Roesch, Matthew R.
author_facet Lee, Brian
Gentry, Ronny N.
Bissonette, Gregory B.
Herman, Rae J.
Mallon, John J.
Bryden, Daniel W.
Calu, Donna J.
Schoenbaum, Geoffrey
Coutureau, Etienne
Marchand, Alain R.
Khamassi, Mehdi
Roesch, Matthew R.
author_sort Lee, Brian
collection PubMed
description Recent computational models of sign tracking (ST) and goal tracking (GT) have accounted for observations that dopamine (DA) is not necessary for all forms of learning and have provided a set of predictions to further their validity. Among these, a central prediction is that manipulating the intertrial interval (ITI) during autoshaping should change the relative ST-GT proportion as well as DA phasic responses. Here, we tested these predictions and found that lengthening the ITI increased ST, i.e., behavioral engagement with conditioned stimuli (CS) and cue-induced phasic DA release. Importantly, DA release was also present at the time of reward delivery, even after learning, and DA release was correlated with time spent in the food cup during the ITI. During conditioning with shorter ITIs, GT was prominent (i.e., engagement with food cup), and DA release responded to the CS while being absent at the time of reward delivery after learning. Hence, shorter ITIs restored the classical DA reward prediction error (RPE) pattern. These results validate the computational hypotheses, opening new perspectives on the understanding of individual differences in Pavlovian conditioning and DA signaling.
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spelling pubmed-61755312018-10-19 Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release Lee, Brian Gentry, Ronny N. Bissonette, Gregory B. Herman, Rae J. Mallon, John J. Bryden, Daniel W. Calu, Donna J. Schoenbaum, Geoffrey Coutureau, Etienne Marchand, Alain R. Khamassi, Mehdi Roesch, Matthew R. PLoS Biol Short Reports Recent computational models of sign tracking (ST) and goal tracking (GT) have accounted for observations that dopamine (DA) is not necessary for all forms of learning and have provided a set of predictions to further their validity. Among these, a central prediction is that manipulating the intertrial interval (ITI) during autoshaping should change the relative ST-GT proportion as well as DA phasic responses. Here, we tested these predictions and found that lengthening the ITI increased ST, i.e., behavioral engagement with conditioned stimuli (CS) and cue-induced phasic DA release. Importantly, DA release was also present at the time of reward delivery, even after learning, and DA release was correlated with time spent in the food cup during the ITI. During conditioning with shorter ITIs, GT was prominent (i.e., engagement with food cup), and DA release responded to the CS while being absent at the time of reward delivery after learning. Hence, shorter ITIs restored the classical DA reward prediction error (RPE) pattern. These results validate the computational hypotheses, opening new perspectives on the understanding of individual differences in Pavlovian conditioning and DA signaling. Public Library of Science 2018-09-26 /pmc/articles/PMC6175531/ /pubmed/30256785 http://dx.doi.org/10.1371/journal.pbio.2004015 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Short Reports
Lee, Brian
Gentry, Ronny N.
Bissonette, Gregory B.
Herman, Rae J.
Mallon, John J.
Bryden, Daniel W.
Calu, Donna J.
Schoenbaum, Geoffrey
Coutureau, Etienne
Marchand, Alain R.
Khamassi, Mehdi
Roesch, Matthew R.
Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title_full Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title_fullStr Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title_full_unstemmed Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title_short Manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
title_sort manipulating the revision of reward value during the intertrial interval increases sign tracking and dopamine release
topic Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175531/
https://www.ncbi.nlm.nih.gov/pubmed/30256785
http://dx.doi.org/10.1371/journal.pbio.2004015
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