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Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats

States of consciousness have been associated with information integration in the brain as modulated by anesthesia and the ascending arousal system. The present study was designed to test the hypothesis that electrical stimulation of the oral part of the pontine reticular nucleus (PnO) can augment in...

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Autores principales: Pillay, Siveshigan, Vizuete, Jeannette, Liu, Xiping, Juhasz, Gabor, Hudetz, Anthony G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932553/
https://www.ncbi.nlm.nih.gov/pubmed/24605091
http://dx.doi.org/10.3389/fnint.2014.00008
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author Pillay, Siveshigan
Vizuete, Jeannette
Liu, Xiping
Juhasz, Gabor
Hudetz, Anthony G.
author_facet Pillay, Siveshigan
Vizuete, Jeannette
Liu, Xiping
Juhasz, Gabor
Hudetz, Anthony G.
author_sort Pillay, Siveshigan
collection PubMed
description States of consciousness have been associated with information integration in the brain as modulated by anesthesia and the ascending arousal system. The present study was designed to test the hypothesis that electrical stimulation of the oral part of the pontine reticular nucleus (PnO) can augment information integration in the cerebral cortex of anesthetized rats. Extracellular unit activity and local field potentials were recorded in freely moving animals from parietal association (PtA) and secondary visual (V2) cortices via chronically implanted microwire arrays at three levels of anesthesia produced by desflurane: 3.5, 4.5, and 6.0% (where 4.5% corresponds to that critical for the loss of consciousness). Information integration was characterized by integration (multiinformation) and interaction entropy, estimated from the statistical distribution of coincident spike patterns. PnO stimulation elicited electrocortical activation as indicated by the reductions in δ- and θ-band powers at the intermediate level of anesthesia. PnO stimulation augmented integration from 1.13 ± 0.03 to 6.12 ± 1.98 × 10(3) bits and interaction entropy from 0.44 ± 0.11 to 2.18 ± 0.72 × 10(3) bits; these changes were most consistent in the PtA at all desflurane concentrations. Stimulation of the retina with discrete light flashes after PnO stimulation elicited an additional 166 ± 25 and 92 ± 12% increase in interaction entropy in V2 during light and intermediate levels. The results suggest that the PnO may modulate spontaneous ongoing and sensory stimulus-related cortical information integration under anesthesia.
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spelling pubmed-39325532014-03-06 Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats Pillay, Siveshigan Vizuete, Jeannette Liu, Xiping Juhasz, Gabor Hudetz, Anthony G. Front Integr Neurosci Neuroscience States of consciousness have been associated with information integration in the brain as modulated by anesthesia and the ascending arousal system. The present study was designed to test the hypothesis that electrical stimulation of the oral part of the pontine reticular nucleus (PnO) can augment information integration in the cerebral cortex of anesthetized rats. Extracellular unit activity and local field potentials were recorded in freely moving animals from parietal association (PtA) and secondary visual (V2) cortices via chronically implanted microwire arrays at three levels of anesthesia produced by desflurane: 3.5, 4.5, and 6.0% (where 4.5% corresponds to that critical for the loss of consciousness). Information integration was characterized by integration (multiinformation) and interaction entropy, estimated from the statistical distribution of coincident spike patterns. PnO stimulation elicited electrocortical activation as indicated by the reductions in δ- and θ-band powers at the intermediate level of anesthesia. PnO stimulation augmented integration from 1.13 ± 0.03 to 6.12 ± 1.98 × 10(3) bits and interaction entropy from 0.44 ± 0.11 to 2.18 ± 0.72 × 10(3) bits; these changes were most consistent in the PtA at all desflurane concentrations. Stimulation of the retina with discrete light flashes after PnO stimulation elicited an additional 166 ± 25 and 92 ± 12% increase in interaction entropy in V2 during light and intermediate levels. The results suggest that the PnO may modulate spontaneous ongoing and sensory stimulus-related cortical information integration under anesthesia. Frontiers Media S.A. 2014-02-24 /pmc/articles/PMC3932553/ /pubmed/24605091 http://dx.doi.org/10.3389/fnint.2014.00008 Text en Copyright © 2014 Pillay, Vizuete, Liu, Juhasz and Hudetz. http://creativecommons.org/licenses/by/3.0/ 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
Pillay, Siveshigan
Vizuete, Jeannette
Liu, Xiping
Juhasz, Gabor
Hudetz, Anthony G.
Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title_full Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title_fullStr Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title_full_unstemmed Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title_short Brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
title_sort brainstem stimulation augments information integration in the cerebral cortex of desflurane-anesthetized rats
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932553/
https://www.ncbi.nlm.nih.gov/pubmed/24605091
http://dx.doi.org/10.3389/fnint.2014.00008
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