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Task-phase-specific dynamics of basal forebrain neuronal ensembles
Cortically projecting basal forebrain neurons play a critical role in learning and attention, and their degeneration accompanies age-related impairments in cognition. Despite the impressive anatomical and cell-type complexity of this system, currently available data suggest that basal forebrain neur...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173808/ https://www.ncbi.nlm.nih.gov/pubmed/25309352 http://dx.doi.org/10.3389/fnsys.2014.00174 |
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author | Tingley, David Alexander, Andrew S. Kolbu, Sean de Sa, Virginia R. Chiba, Andrea A. Nitz, Douglas A. |
author_facet | Tingley, David Alexander, Andrew S. Kolbu, Sean de Sa, Virginia R. Chiba, Andrea A. Nitz, Douglas A. |
author_sort | Tingley, David |
collection | PubMed |
description | Cortically projecting basal forebrain neurons play a critical role in learning and attention, and their degeneration accompanies age-related impairments in cognition. Despite the impressive anatomical and cell-type complexity of this system, currently available data suggest that basal forebrain neurons lack complexity in their response fields, with activity primarily reflecting only macro-level brain states such as sleep and wake, onset of relevant stimuli and/or reward obtainment. The current study examined the spiking activity of basal forebrain neuron populations across multiple phases of a selective attention task, addressing, in particular, the issue of complexity in ensemble firing patterns across time. Clustering techniques applied to the full population revealed a large number of distinct categories of task-phase-specific activity patterns. Unique population firing-rate vectors defined each task phase and most categories of task-phase-specific firing had counterparts with opposing firing patterns. An analogous set of task-phase-specific firing patterns was also observed in a population of posterior parietal cortex neurons. Thus, consistent with the known anatomical complexity, basal forebrain population dynamics are capable of differentially modulating their cortical targets according to the unique sets of environmental stimuli, motor requirements, and cognitive processes associated with different task phases. |
format | Online Article Text |
id | pubmed-4173808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41738082014-10-10 Task-phase-specific dynamics of basal forebrain neuronal ensembles Tingley, David Alexander, Andrew S. Kolbu, Sean de Sa, Virginia R. Chiba, Andrea A. Nitz, Douglas A. Front Syst Neurosci Neuroscience Cortically projecting basal forebrain neurons play a critical role in learning and attention, and their degeneration accompanies age-related impairments in cognition. Despite the impressive anatomical and cell-type complexity of this system, currently available data suggest that basal forebrain neurons lack complexity in their response fields, with activity primarily reflecting only macro-level brain states such as sleep and wake, onset of relevant stimuli and/or reward obtainment. The current study examined the spiking activity of basal forebrain neuron populations across multiple phases of a selective attention task, addressing, in particular, the issue of complexity in ensemble firing patterns across time. Clustering techniques applied to the full population revealed a large number of distinct categories of task-phase-specific activity patterns. Unique population firing-rate vectors defined each task phase and most categories of task-phase-specific firing had counterparts with opposing firing patterns. An analogous set of task-phase-specific firing patterns was also observed in a population of posterior parietal cortex neurons. Thus, consistent with the known anatomical complexity, basal forebrain population dynamics are capable of differentially modulating their cortical targets according to the unique sets of environmental stimuli, motor requirements, and cognitive processes associated with different task phases. Frontiers Media S.A. 2014-09-24 /pmc/articles/PMC4173808/ /pubmed/25309352 http://dx.doi.org/10.3389/fnsys.2014.00174 Text en Copyright © 2014 Tingley, Alexander, Kolbu, de Sa, Chiba and Nitz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Tingley, David Alexander, Andrew S. Kolbu, Sean de Sa, Virginia R. Chiba, Andrea A. Nitz, Douglas A. Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title | Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title_full | Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title_fullStr | Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title_full_unstemmed | Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title_short | Task-phase-specific dynamics of basal forebrain neuronal ensembles |
title_sort | task-phase-specific dynamics of basal forebrain neuronal ensembles |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173808/ https://www.ncbi.nlm.nih.gov/pubmed/25309352 http://dx.doi.org/10.3389/fnsys.2014.00174 |
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