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A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell
The nucleus accumbens shell (NAcSh) is critically important for reward valuations, yet it remains unclear how valuation information is integrated in this region to drive behaviour during reinforcement learning. Using an optogenetic spatial self-stimulation task in mice, here we show that contingent...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886947/ https://www.ncbi.nlm.nih.gov/pubmed/36717646 http://dx.doi.org/10.1038/s42003-023-04429-6 |
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author | Lind, Erin B. Sweis, Brian M. Asp, Anders J. Esguerra, Manuel Silvis, Keelia A. David Redish, A. Thomas, Mark J. |
author_facet | Lind, Erin B. Sweis, Brian M. Asp, Anders J. Esguerra, Manuel Silvis, Keelia A. David Redish, A. Thomas, Mark J. |
author_sort | Lind, Erin B. |
collection | PubMed |
description | The nucleus accumbens shell (NAcSh) is critically important for reward valuations, yet it remains unclear how valuation information is integrated in this region to drive behaviour during reinforcement learning. Using an optogenetic spatial self-stimulation task in mice, here we show that contingent activation of different excitatory inputs to the NAcSh change expression of different reward-related behaviours. Our data indicate that medial prefrontal inputs support place preference via repeated actions, ventral hippocampal inputs consistently promote place preferences, basolateral amygdala inputs produce modest place preferences but as a byproduct of increased sensitivity to time investments, and paraventricular inputs reduce place preferences yet do not produce full avoidance behaviour. These findings suggest that each excitatory input provides distinct information to the NAcSh, and we propose that this reflects the reinforcement of different credit assignment functions. Our finding of a quadruple dissociation of NAcSh input-specific behaviours provides insights into how types of information carried by distinct inputs to the NAcSh could be integrated to help drive reinforcement learning and situationally appropriate behavioural responses. |
format | Online Article Text |
id | pubmed-9886947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98869472023-02-01 A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell Lind, Erin B. Sweis, Brian M. Asp, Anders J. Esguerra, Manuel Silvis, Keelia A. David Redish, A. Thomas, Mark J. Commun Biol Article The nucleus accumbens shell (NAcSh) is critically important for reward valuations, yet it remains unclear how valuation information is integrated in this region to drive behaviour during reinforcement learning. Using an optogenetic spatial self-stimulation task in mice, here we show that contingent activation of different excitatory inputs to the NAcSh change expression of different reward-related behaviours. Our data indicate that medial prefrontal inputs support place preference via repeated actions, ventral hippocampal inputs consistently promote place preferences, basolateral amygdala inputs produce modest place preferences but as a byproduct of increased sensitivity to time investments, and paraventricular inputs reduce place preferences yet do not produce full avoidance behaviour. These findings suggest that each excitatory input provides distinct information to the NAcSh, and we propose that this reflects the reinforcement of different credit assignment functions. Our finding of a quadruple dissociation of NAcSh input-specific behaviours provides insights into how types of information carried by distinct inputs to the NAcSh could be integrated to help drive reinforcement learning and situationally appropriate behavioural responses. Nature Publishing Group UK 2023-01-30 /pmc/articles/PMC9886947/ /pubmed/36717646 http://dx.doi.org/10.1038/s42003-023-04429-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lind, Erin B. Sweis, Brian M. Asp, Anders J. Esguerra, Manuel Silvis, Keelia A. David Redish, A. Thomas, Mark J. A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title | A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title_full | A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title_fullStr | A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title_full_unstemmed | A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title_short | A quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
title_sort | quadruple dissociation of reward-related behaviour in mice across excitatory inputs to the nucleus accumbens shell |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9886947/ https://www.ncbi.nlm.nih.gov/pubmed/36717646 http://dx.doi.org/10.1038/s42003-023-04429-6 |
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