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Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro

Acetylcholine is the primary neuromodulator involved in cortical arousal in mammals. Cholinergic modulation is involved in conscious awareness, memory formation and attention – processes that involve intercommunication between different cortical regions. Such communication is achieved in part throug...

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Detalles Bibliográficos
Autores principales: Roopun, Anita K., LeBeau, Fiona E.N., Rammell, James, Cunningham, Mark O., Traub, Roger D., Whittington, Miles A.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856628/
https://www.ncbi.nlm.nih.gov/pubmed/20407636
http://dx.doi.org/10.3389/fncir.2010.00008
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author Roopun, Anita K.
LeBeau, Fiona E.N.
Rammell, James
Cunningham, Mark O.
Traub, Roger D.
Whittington, Miles A.
author_facet Roopun, Anita K.
LeBeau, Fiona E.N.
Rammell, James
Cunningham, Mark O.
Traub, Roger D.
Whittington, Miles A.
author_sort Roopun, Anita K.
collection PubMed
description Acetylcholine is the primary neuromodulator involved in cortical arousal in mammals. Cholinergic modulation is involved in conscious awareness, memory formation and attention – processes that involve intercommunication between different cortical regions. Such communication is achieved in part through temporal structuring of neuronal activity by population rhythms, particularly in the beta and gamma frequency ranges (12–80 Hz). Here we demonstrate, using in vitro and in silico models, that spectrally identical patterns of beta2 and gamma rhythms are generated in primary sensory areas and polymodal association areas by fundamentally different local circuit mechanisms: Glutamatergic excitation induced beta2 frequency population rhythms only in layer 5 association cortex whereas cholinergic neuromodulation induced this rhythm only in layer 5 primary sensory cortex. This region-specific sensitivity of local circuits to cholinergic modulation allowed for control of the extent of cortical temporal interactions. Furthermore, the contrasting mechanisms underlying these beta2 rhythms produced a high degree of directionality, favouring an influence of association cortex over primary auditory cortex.
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spelling pubmed-28566282010-04-20 Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro Roopun, Anita K. LeBeau, Fiona E.N. Rammell, James Cunningham, Mark O. Traub, Roger D. Whittington, Miles A. Front Neural Circuits Neuroscience Acetylcholine is the primary neuromodulator involved in cortical arousal in mammals. Cholinergic modulation is involved in conscious awareness, memory formation and attention – processes that involve intercommunication between different cortical regions. Such communication is achieved in part through temporal structuring of neuronal activity by population rhythms, particularly in the beta and gamma frequency ranges (12–80 Hz). Here we demonstrate, using in vitro and in silico models, that spectrally identical patterns of beta2 and gamma rhythms are generated in primary sensory areas and polymodal association areas by fundamentally different local circuit mechanisms: Glutamatergic excitation induced beta2 frequency population rhythms only in layer 5 association cortex whereas cholinergic neuromodulation induced this rhythm only in layer 5 primary sensory cortex. This region-specific sensitivity of local circuits to cholinergic modulation allowed for control of the extent of cortical temporal interactions. Furthermore, the contrasting mechanisms underlying these beta2 rhythms produced a high degree of directionality, favouring an influence of association cortex over primary auditory cortex. Frontiers Research Foundation 2010-03-22 /pmc/articles/PMC2856628/ /pubmed/20407636 http://dx.doi.org/10.3389/fncir.2010.00008 Text en Copyright © 2010 Roopun, LeBeau, Rammell, Cunningham, Traub and Whittington. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Roopun, Anita K.
LeBeau, Fiona E.N.
Rammell, James
Cunningham, Mark O.
Traub, Roger D.
Whittington, Miles A.
Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title_full Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title_fullStr Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title_full_unstemmed Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title_short Cholinergic Neuromodulation Controls Directed Temporal Communication in Neocortex in Vitro
title_sort cholinergic neuromodulation controls directed temporal communication in neocortex in vitro
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856628/
https://www.ncbi.nlm.nih.gov/pubmed/20407636
http://dx.doi.org/10.3389/fncir.2010.00008
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