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Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making
Distributed brain networks govern adaptive decision‐making, new learning and rapid updating of information. However, the functional contribution of the rhesus macaque monkey parvocellular nucleus of the mediodorsal thalamus (MDpc) in these key higher cognitive processes remains unknown. This study i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519510/ https://www.ncbi.nlm.nih.gov/pubmed/30022540 http://dx.doi.org/10.1111/ejn.14078 |
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author | Chakraborty, Subhojit Ouhaz, Zakaria Mason, Stuart Mitchell, Anna S. |
author_facet | Chakraborty, Subhojit Ouhaz, Zakaria Mason, Stuart Mitchell, Anna S. |
author_sort | Chakraborty, Subhojit |
collection | PubMed |
description | Distributed brain networks govern adaptive decision‐making, new learning and rapid updating of information. However, the functional contribution of the rhesus macaque monkey parvocellular nucleus of the mediodorsal thalamus (MDpc) in these key higher cognitive processes remains unknown. This study investigated the impact of MDpc damage in cognition. Preoperatively, animals were trained on an object‐in‐place scene discrimination task that assesses rapid learning of novel information within each session. Bilateral neurotoxic (NMDA and ibotenic acid) MDpc lesions did not impair new learning unless the monkey had also sustained damage to the magnocellular division of the MD (MDmc). Contralateral unilateral MDpc and MDmc damage also impaired new learning, while selective unilateral MDmc damage produced new learning deficits that eventually resolved with repeated testing. In contrast, during food reward (satiety) devaluation, monkeys with either bilateral MDpc damage or combined MDpc and MDmc damage showed attenuated food reward preferences compared to unoperated control monkeys; the selective unilateral MDmc damage left performance intact. Our preliminary results demonstrate selective dissociable roles for the two adjacent nuclei of the primate MD, namely, MDpc, as part of a frontal cortical network, and the MDmc, as part of a frontal‐temporal cortical network, in learning, memory and the cognitive control of behavioural choices after changes in reward value. Moreover, the functional cognitive deficits produced after differing MD damage show that the different subdivisions of the MD thalamus support distributed neural networks to rapidly and fluidly incorporate task‐relevant information, in order to optimise the animals’ ability to receive rewards. |
format | Online Article Text |
id | pubmed-6519510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65195102019-05-23 Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making Chakraborty, Subhojit Ouhaz, Zakaria Mason, Stuart Mitchell, Anna S. Eur J Neurosci Ray Guillery Special Issue Distributed brain networks govern adaptive decision‐making, new learning and rapid updating of information. However, the functional contribution of the rhesus macaque monkey parvocellular nucleus of the mediodorsal thalamus (MDpc) in these key higher cognitive processes remains unknown. This study investigated the impact of MDpc damage in cognition. Preoperatively, animals were trained on an object‐in‐place scene discrimination task that assesses rapid learning of novel information within each session. Bilateral neurotoxic (NMDA and ibotenic acid) MDpc lesions did not impair new learning unless the monkey had also sustained damage to the magnocellular division of the MD (MDmc). Contralateral unilateral MDpc and MDmc damage also impaired new learning, while selective unilateral MDmc damage produced new learning deficits that eventually resolved with repeated testing. In contrast, during food reward (satiety) devaluation, monkeys with either bilateral MDpc damage or combined MDpc and MDmc damage showed attenuated food reward preferences compared to unoperated control monkeys; the selective unilateral MDmc damage left performance intact. Our preliminary results demonstrate selective dissociable roles for the two adjacent nuclei of the primate MD, namely, MDpc, as part of a frontal cortical network, and the MDmc, as part of a frontal‐temporal cortical network, in learning, memory and the cognitive control of behavioural choices after changes in reward value. Moreover, the functional cognitive deficits produced after differing MD damage show that the different subdivisions of the MD thalamus support distributed neural networks to rapidly and fluidly incorporate task‐relevant information, in order to optimise the animals’ ability to receive rewards. John Wiley and Sons Inc. 2018-08-16 2019-04 /pmc/articles/PMC6519510/ /pubmed/30022540 http://dx.doi.org/10.1111/ejn.14078 Text en © 2018 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Ray Guillery Special Issue Chakraborty, Subhojit Ouhaz, Zakaria Mason, Stuart Mitchell, Anna S. Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title | Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title_full | Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title_fullStr | Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title_full_unstemmed | Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title_short | Macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
title_sort | macaque parvocellular mediodorsal thalamus: dissociable contributions to learning and adaptive decision‐making |
topic | Ray Guillery Special Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519510/ https://www.ncbi.nlm.nih.gov/pubmed/30022540 http://dx.doi.org/10.1111/ejn.14078 |
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