Cargando…
Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex
In an uncertain world, the ability to predict and update the relationships between environmental cues and outcomes is a fundamental element of adaptive behaviour. This type of learning is typically thought to depend on prediction error, the difference between expected and experienced events and in t...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075902/ https://www.ncbi.nlm.nih.gov/pubmed/31703234 http://dx.doi.org/10.1038/s41386-019-0564-8 |
_version_ | 1783507111922106368 |
---|---|
author | Werlen, Emilie Shin, Soon-Lim Gastambide, Francois Francois, Jennifer Tricklebank, Mark D. Marston, Hugh M. Huxter, John R. Gilmour, Gary Walton, Mark E. |
author_facet | Werlen, Emilie Shin, Soon-Lim Gastambide, Francois Francois, Jennifer Tricklebank, Mark D. Marston, Hugh M. Huxter, John R. Gilmour, Gary Walton, Mark E. |
author_sort | Werlen, Emilie |
collection | PubMed |
description | In an uncertain world, the ability to predict and update the relationships between environmental cues and outcomes is a fundamental element of adaptive behaviour. This type of learning is typically thought to depend on prediction error, the difference between expected and experienced events and in the reward domain that has been closely linked to mesolimbic dopamine. There is also increasing behavioural and neuroimaging evidence that disruption to this process may be a cross-diagnostic feature of several neuropsychiatric and neurological disorders in which dopamine is dysregulated. However, the precise relationship between haemodynamic measures, dopamine and reward-guided learning remains unclear. To help address this issue, we used a translational technique, oxygen amperometry, to record haemodynamic signals in the nucleus accumbens (NAc) and orbitofrontal cortex (OFC), while freely moving rats performed a probabilistic Pavlovian learning task. Using a model-based analysis approach to account for individual variations in learning, we found that the oxygen signal in the NAc correlated with a reward prediction error, whereas in the OFC it correlated with an unsigned prediction error or salience signal. Furthermore, an acute dose of amphetamine, creating a hyperdopaminergic state, disrupted rats’ ability to discriminate between cues associated with either a high or a low probability of reward and concomitantly corrupted prediction error signalling. These results demonstrate parallel but distinct prediction error signals in NAc and OFC during learning, both of which are affected by psychostimulant administration. Furthermore, they establish the viability of tracking and manipulating haemodynamic signatures of reward-guided learning observed in human fMRI studies by using a proxy signal for BOLD in a freely behaving rodent. |
format | Online Article Text |
id | pubmed-7075902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-70759022020-03-18 Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex Werlen, Emilie Shin, Soon-Lim Gastambide, Francois Francois, Jennifer Tricklebank, Mark D. Marston, Hugh M. Huxter, John R. Gilmour, Gary Walton, Mark E. Neuropsychopharmacology Article In an uncertain world, the ability to predict and update the relationships between environmental cues and outcomes is a fundamental element of adaptive behaviour. This type of learning is typically thought to depend on prediction error, the difference between expected and experienced events and in the reward domain that has been closely linked to mesolimbic dopamine. There is also increasing behavioural and neuroimaging evidence that disruption to this process may be a cross-diagnostic feature of several neuropsychiatric and neurological disorders in which dopamine is dysregulated. However, the precise relationship between haemodynamic measures, dopamine and reward-guided learning remains unclear. To help address this issue, we used a translational technique, oxygen amperometry, to record haemodynamic signals in the nucleus accumbens (NAc) and orbitofrontal cortex (OFC), while freely moving rats performed a probabilistic Pavlovian learning task. Using a model-based analysis approach to account for individual variations in learning, we found that the oxygen signal in the NAc correlated with a reward prediction error, whereas in the OFC it correlated with an unsigned prediction error or salience signal. Furthermore, an acute dose of amphetamine, creating a hyperdopaminergic state, disrupted rats’ ability to discriminate between cues associated with either a high or a low probability of reward and concomitantly corrupted prediction error signalling. These results demonstrate parallel but distinct prediction error signals in NAc and OFC during learning, both of which are affected by psychostimulant administration. Furthermore, they establish the viability of tracking and manipulating haemodynamic signatures of reward-guided learning observed in human fMRI studies by using a proxy signal for BOLD in a freely behaving rodent. Springer International Publishing 2019-11-08 2020-04 /pmc/articles/PMC7075902/ /pubmed/31703234 http://dx.doi.org/10.1038/s41386-019-0564-8 Text en © The Author(s) 2019 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 Werlen, Emilie Shin, Soon-Lim Gastambide, Francois Francois, Jennifer Tricklebank, Mark D. Marston, Hugh M. Huxter, John R. Gilmour, Gary Walton, Mark E. Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title | Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title_full | Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title_fullStr | Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title_full_unstemmed | Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title_short | Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
title_sort | amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075902/ https://www.ncbi.nlm.nih.gov/pubmed/31703234 http://dx.doi.org/10.1038/s41386-019-0564-8 |
work_keys_str_mv | AT werlenemilie amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT shinsoonlim amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT gastambidefrancois amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT francoisjennifer amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT tricklebankmarkd amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT marstonhughm amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT huxterjohnr amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT gilmourgary amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex AT waltonmarke amphetaminedisruptshaemodynamiccorrelatesofpredictionerrorsinnucleusaccumbensandorbitofrontalcortex |