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Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum
The nucleus accumbens core (NAc) is important for integrating and providing information to downstream areas about the timing and value of anticipated reward. Although NAc is one of the first brain regions to be affected by drugs of abuse, we still do not know how neural correlates related to reward...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180050/ https://www.ncbi.nlm.nih.gov/pubmed/29728645 http://dx.doi.org/10.1038/s41386-018-0058-0 |
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author | Burton, Amanda C. Bissonette, Gregory B. Vazquez, Daniela Blume, Elyse M. Donnelly, Maria Heatley, Kendall C. Hinduja, Abhishek Roesch, Matthew R. |
author_facet | Burton, Amanda C. Bissonette, Gregory B. Vazquez, Daniela Blume, Elyse M. Donnelly, Maria Heatley, Kendall C. Hinduja, Abhishek Roesch, Matthew R. |
author_sort | Burton, Amanda C. |
collection | PubMed |
description | The nucleus accumbens core (NAc) is important for integrating and providing information to downstream areas about the timing and value of anticipated reward. Although NAc is one of the first brain regions to be affected by drugs of abuse, we still do not know how neural correlates related to reward expectancy are affected by previous cocaine self-administration. To address this issue, we recorded from single neurons in the NAc of rats that had previously self-administered cocaine or sucrose (control). Neural recordings were then taken while rats performed an odor-guided decision-making task in which we independently manipulated value of expected reward by changing the delay to or size of reward across a series of trial blocks. We found that previous cocaine self-administration made rats more impulsive, biasing choice behavior toward more immediate reward. Further, compared to controls, cocaine-exposed rats showed significantly fewer neurons in the NAc that were responsive during odor cues and reward delivery, and in the reward-responsive neurons that remained, diminished directional and value encoding was observed. Lastly, we found that after cocaine exposure, reward-related firing during longer delays was reduced compared to controls. These results demonstrate that prior cocaine self-administration alters reward-expectancy encoding in NAc, which could contribute to poor decision making observed after chronic cocaine use. |
format | Online Article Text |
id | pubmed-6180050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-61800502018-10-15 Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum Burton, Amanda C. Bissonette, Gregory B. Vazquez, Daniela Blume, Elyse M. Donnelly, Maria Heatley, Kendall C. Hinduja, Abhishek Roesch, Matthew R. Neuropsychopharmacology Article The nucleus accumbens core (NAc) is important for integrating and providing information to downstream areas about the timing and value of anticipated reward. Although NAc is one of the first brain regions to be affected by drugs of abuse, we still do not know how neural correlates related to reward expectancy are affected by previous cocaine self-administration. To address this issue, we recorded from single neurons in the NAc of rats that had previously self-administered cocaine or sucrose (control). Neural recordings were then taken while rats performed an odor-guided decision-making task in which we independently manipulated value of expected reward by changing the delay to or size of reward across a series of trial blocks. We found that previous cocaine self-administration made rats more impulsive, biasing choice behavior toward more immediate reward. Further, compared to controls, cocaine-exposed rats showed significantly fewer neurons in the NAc that were responsive during odor cues and reward delivery, and in the reward-responsive neurons that remained, diminished directional and value encoding was observed. Lastly, we found that after cocaine exposure, reward-related firing during longer delays was reduced compared to controls. These results demonstrate that prior cocaine self-administration alters reward-expectancy encoding in NAc, which could contribute to poor decision making observed after chronic cocaine use. Springer International Publishing 2018-04-10 2018-11 /pmc/articles/PMC6180050/ /pubmed/29728645 http://dx.doi.org/10.1038/s41386-018-0058-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Burton, Amanda C. Bissonette, Gregory B. Vazquez, Daniela Blume, Elyse M. Donnelly, Maria Heatley, Kendall C. Hinduja, Abhishek Roesch, Matthew R. Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title | Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title_full | Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title_fullStr | Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title_full_unstemmed | Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title_short | Previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
title_sort | previous cocaine self-administration disrupts reward expectancy encoding in ventral striatum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180050/ https://www.ncbi.nlm.nih.gov/pubmed/29728645 http://dx.doi.org/10.1038/s41386-018-0058-0 |
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