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Linking brain activity across scales with simultaneous opto- and electrophysiology
The brain enables adaptive behavior via the dynamic coordination of diverse neuronal signals across spatial and temporal scales: from fast action potential patterns in microcircuits to slower patterns of distributed activity in brain-wide networks. Understanding principles of multiscale dynamics req...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472193/ https://www.ncbi.nlm.nih.gov/pubmed/37662552 http://dx.doi.org/10.1117/1.NPh.11.3.033403 |
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author | Lewis, Christopher M. Hoffmann, Adrian Helmchen, Fritjof |
author_facet | Lewis, Christopher M. Hoffmann, Adrian Helmchen, Fritjof |
author_sort | Lewis, Christopher M. |
collection | PubMed |
description | The brain enables adaptive behavior via the dynamic coordination of diverse neuronal signals across spatial and temporal scales: from fast action potential patterns in microcircuits to slower patterns of distributed activity in brain-wide networks. Understanding principles of multiscale dynamics requires simultaneous monitoring of signals in multiple, distributed network nodes. Combining optical and electrical recordings of brain activity is promising for collecting data across multiple scales and can reveal aspects of coordinated dynamics invisible to standard, single-modality approaches. We review recent progress in combining opto- and electrophysiology, focusing on mouse studies that shed new light on the function of single neurons by embedding their activity in the context of brain-wide activity patterns. Optical and electrical readouts can be tailored to desired scales to tackle specific questions. For example, fast dynamics in single cells or local populations recorded with multi-electrode arrays can be related to simultaneously acquired optical signals that report activity in specified subpopulations of neurons, in non-neuronal cells, or in neuromodulatory pathways. Conversely, two-photon imaging can be used to densely monitor activity in local circuits while sampling electrical activity in distant brain areas at the same time. The refinement of combined approaches will continue to reveal previously inaccessible and under-appreciated aspects of coordinated brain activity. |
format | Online Article Text |
id | pubmed-10472193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-104721932023-09-02 Linking brain activity across scales with simultaneous opto- and electrophysiology Lewis, Christopher M. Hoffmann, Adrian Helmchen, Fritjof Neurophotonics Special Section on Understanding of Neural Circuits with Neurophotonics The brain enables adaptive behavior via the dynamic coordination of diverse neuronal signals across spatial and temporal scales: from fast action potential patterns in microcircuits to slower patterns of distributed activity in brain-wide networks. Understanding principles of multiscale dynamics requires simultaneous monitoring of signals in multiple, distributed network nodes. Combining optical and electrical recordings of brain activity is promising for collecting data across multiple scales and can reveal aspects of coordinated dynamics invisible to standard, single-modality approaches. We review recent progress in combining opto- and electrophysiology, focusing on mouse studies that shed new light on the function of single neurons by embedding their activity in the context of brain-wide activity patterns. Optical and electrical readouts can be tailored to desired scales to tackle specific questions. For example, fast dynamics in single cells or local populations recorded with multi-electrode arrays can be related to simultaneously acquired optical signals that report activity in specified subpopulations of neurons, in non-neuronal cells, or in neuromodulatory pathways. Conversely, two-photon imaging can be used to densely monitor activity in local circuits while sampling electrical activity in distant brain areas at the same time. The refinement of combined approaches will continue to reveal previously inaccessible and under-appreciated aspects of coordinated brain activity. Society of Photo-Optical Instrumentation Engineers 2023-09-01 2024-09 /pmc/articles/PMC10472193/ /pubmed/37662552 http://dx.doi.org/10.1117/1.NPh.11.3.033403 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/Published by SPIE under a Creative Commons Attribution 4.0 International License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Special Section on Understanding of Neural Circuits with Neurophotonics Lewis, Christopher M. Hoffmann, Adrian Helmchen, Fritjof Linking brain activity across scales with simultaneous opto- and electrophysiology |
title | Linking brain activity across scales with simultaneous opto- and electrophysiology |
title_full | Linking brain activity across scales with simultaneous opto- and electrophysiology |
title_fullStr | Linking brain activity across scales with simultaneous opto- and electrophysiology |
title_full_unstemmed | Linking brain activity across scales with simultaneous opto- and electrophysiology |
title_short | Linking brain activity across scales with simultaneous opto- and electrophysiology |
title_sort | linking brain activity across scales with simultaneous opto- and electrophysiology |
topic | Special Section on Understanding of Neural Circuits with Neurophotonics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472193/ https://www.ncbi.nlm.nih.gov/pubmed/37662552 http://dx.doi.org/10.1117/1.NPh.11.3.033403 |
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