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Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex
Fluctuations in brain and behavioral state are supported by broadly projecting neuromodulatory systems. In this study, we use mesoscale two-photon calcium imaging to examine spontaneous activity of cholinergic and noradrenergic axons in awake mice in order to determine the interaction between arousa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238096/ https://www.ncbi.nlm.nih.gov/pubmed/37102362 http://dx.doi.org/10.7554/eLife.81826 |
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author | Collins, Lindsay Francis, John Emanuel, Brett McCormick, David A |
author_facet | Collins, Lindsay Francis, John Emanuel, Brett McCormick, David A |
author_sort | Collins, Lindsay |
collection | PubMed |
description | Fluctuations in brain and behavioral state are supported by broadly projecting neuromodulatory systems. In this study, we use mesoscale two-photon calcium imaging to examine spontaneous activity of cholinergic and noradrenergic axons in awake mice in order to determine the interaction between arousal/movement state transitions and neuromodulatory activity across the dorsal cortex at distances separated by up to 4 mm. We confirm that GCaMP6s activity within axonal projections of both basal forebrain cholinergic and locus coeruleus noradrenergic neurons track arousal, indexed as pupil diameter, and changes in behavioral engagement, as reflected by bouts of whisker movement and/or locomotion. The broad coordination in activity between even distant axonal segments indicates that both of these systems can communicate, in part, through a global signal, especially in relation to changes in behavioral state. In addition to this broadly coordinated activity, we also find evidence that a subpopulation of both cholinergic and noradrenergic axons may exhibit heterogeneity in activity that appears to be independent of our measures of behavioral state. By monitoring the activity of cholinergic interneurons in the cortex, we found that a subpopulation of these cells also exhibit state-dependent (arousal/movement) activity. These results demonstrate that cholinergic and noradrenergic systems provide a prominent and broadly synchronized signal related to behavioral state, and therefore may contribute to state-dependent cortical activity and excitability. |
format | Online Article Text |
id | pubmed-10238096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-102380962023-06-03 Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex Collins, Lindsay Francis, John Emanuel, Brett McCormick, David A eLife Neuroscience Fluctuations in brain and behavioral state are supported by broadly projecting neuromodulatory systems. In this study, we use mesoscale two-photon calcium imaging to examine spontaneous activity of cholinergic and noradrenergic axons in awake mice in order to determine the interaction between arousal/movement state transitions and neuromodulatory activity across the dorsal cortex at distances separated by up to 4 mm. We confirm that GCaMP6s activity within axonal projections of both basal forebrain cholinergic and locus coeruleus noradrenergic neurons track arousal, indexed as pupil diameter, and changes in behavioral engagement, as reflected by bouts of whisker movement and/or locomotion. The broad coordination in activity between even distant axonal segments indicates that both of these systems can communicate, in part, through a global signal, especially in relation to changes in behavioral state. In addition to this broadly coordinated activity, we also find evidence that a subpopulation of both cholinergic and noradrenergic axons may exhibit heterogeneity in activity that appears to be independent of our measures of behavioral state. By monitoring the activity of cholinergic interneurons in the cortex, we found that a subpopulation of these cells also exhibit state-dependent (arousal/movement) activity. These results demonstrate that cholinergic and noradrenergic systems provide a prominent and broadly synchronized signal related to behavioral state, and therefore may contribute to state-dependent cortical activity and excitability. eLife Sciences Publications, Ltd 2023-04-27 /pmc/articles/PMC10238096/ /pubmed/37102362 http://dx.doi.org/10.7554/eLife.81826 Text en © 2023, Collins et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Collins, Lindsay Francis, John Emanuel, Brett McCormick, David A Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title | Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title_full | Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title_fullStr | Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title_full_unstemmed | Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title_short | Cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
title_sort | cholinergic and noradrenergic axonal activity contains a behavioral-state signal that is coordinated across the dorsal cortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238096/ https://www.ncbi.nlm.nih.gov/pubmed/37102362 http://dx.doi.org/10.7554/eLife.81826 |
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