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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...

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Autores principales: Tingley, David, Alexander, Andrew S., Kolbu, Sean, de Sa, Virginia R., Chiba, Andrea A., Nitz, Douglas A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
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.
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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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