Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783486462214275072 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6952529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT brierlindseym separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT landsnessericc separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT snyderabrahamz separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT wrightpatrickw separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT baxtergranta separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT baueradamq separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT leejinmoo separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia AT culverjosephp separabilityofcalciumslowwavesandfunctionalconnectivityduringwakesleepandanesthesia |