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Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia

Modulation of brain state, e.g., by anesthesia, alters the correlation structure of spontaneous activity, especially in the delta band. This effect has largely been attributed to the [Formula: see text] slow oscillation that is characteristic of anesthesia and nonrapid eye movement (NREM) sleep. How...

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Autores principales: Brier, Lindsey M., Landsness, Eric C., Snyder, Abraham Z., Wright, Patrick W., Baxter, Grant A., Bauer, Adam Q., Lee, Jin-Moo, Culver, Joseph P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952529/
https://www.ncbi.nlm.nih.gov/pubmed/31930154
http://dx.doi.org/10.1117/1.NPh.6.3.035002
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author Brier, Lindsey M.
Landsness, Eric C.
Snyder, Abraham Z.
Wright, Patrick W.
Baxter, Grant A.
Bauer, Adam Q.
Lee, Jin-Moo
Culver, Joseph P.
author_facet Brier, Lindsey M.
Landsness, Eric C.
Snyder, Abraham Z.
Wright, Patrick W.
Baxter, Grant A.
Bauer, Adam Q.
Lee, Jin-Moo
Culver, Joseph P.
author_sort Brier, Lindsey M.
collection PubMed
description Modulation of brain state, e.g., by anesthesia, alters the correlation structure of spontaneous activity, especially in the delta band. This effect has largely been attributed to the [Formula: see text] slow oscillation that is characteristic of anesthesia and nonrapid eye movement (NREM) sleep. However, the effect of the slow oscillation on correlation structures and the spectral content of spontaneous activity across brain states (including NREM) has not been comprehensively examined. Further, discrepancies between activity dynamics observed with hemoglobin versus calcium (GCaMP6) imaging have not been reconciled. Lastly, whether the slow oscillation replaces functional connectivity (FC) patterns typical of the alert state, or superimposes on them, remains unclear. Here, we use wide-field calcium imaging to study spontaneous cortical activity in awake, anesthetized, and naturally sleeping mice. We find modest brain state-dependent changes in infraslow correlations but larger changes in GCaMP6 delta correlations. Principal component analysis of GCaMP6 sleep/anesthesia data in the delta band revealed that the slow oscillation is largely confined to the first three components. Removal of these components revealed a correlation structure strikingly similar to that observed during wake. These results indicate that, during NREM sleep/anesthesia, the slow oscillation superimposes onto a canonical FC architecture.
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spelling pubmed-69525292020-03-18 Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia Brier, Lindsey M. Landsness, Eric C. Snyder, Abraham Z. Wright, Patrick W. Baxter, Grant A. Bauer, Adam Q. Lee, Jin-Moo Culver, Joseph P. Neurophotonics Research Papers Modulation of brain state, e.g., by anesthesia, alters the correlation structure of spontaneous activity, especially in the delta band. This effect has largely been attributed to the [Formula: see text] slow oscillation that is characteristic of anesthesia and nonrapid eye movement (NREM) sleep. However, the effect of the slow oscillation on correlation structures and the spectral content of spontaneous activity across brain states (including NREM) has not been comprehensively examined. Further, discrepancies between activity dynamics observed with hemoglobin versus calcium (GCaMP6) imaging have not been reconciled. Lastly, whether the slow oscillation replaces functional connectivity (FC) patterns typical of the alert state, or superimposes on them, remains unclear. Here, we use wide-field calcium imaging to study spontaneous cortical activity in awake, anesthetized, and naturally sleeping mice. We find modest brain state-dependent changes in infraslow correlations but larger changes in GCaMP6 delta correlations. Principal component analysis of GCaMP6 sleep/anesthesia data in the delta band revealed that the slow oscillation is largely confined to the first three components. Removal of these components revealed a correlation structure strikingly similar to that observed during wake. These results indicate that, during NREM sleep/anesthesia, the slow oscillation superimposes onto a canonical FC architecture. Society of Photo-Optical Instrumentation Engineers 2019-07-13 2019-07 /pmc/articles/PMC6952529/ /pubmed/31930154 http://dx.doi.org/10.1117/1.NPh.6.3.035002 Text en © The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
spellingShingle Research Papers
Brier, Lindsey M.
Landsness, Eric C.
Snyder, Abraham Z.
Wright, Patrick W.
Baxter, Grant A.
Bauer, Adam Q.
Lee, Jin-Moo
Culver, Joseph P.
Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title_full Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title_fullStr Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title_full_unstemmed Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title_short Separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
title_sort separability of calcium slow waves and functional connectivity during wake, sleep, and anesthesia
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952529/
https://www.ncbi.nlm.nih.gov/pubmed/31930154
http://dx.doi.org/10.1117/1.NPh.6.3.035002
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