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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...

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Autores principales: Chakraborty, Subhojit, Ouhaz, Zakaria, Mason, Stuart, Mitchell, Anna S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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.
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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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