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Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice

In vivo electrophysiology is the gold standard technique used to investigate sub-second neural dynamics in freely behaving animals. However, monitoring cell-type-specific population activity is not a trivial task. Over the last decade, fiber photometry based on genetically encoded calcium indicators...

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Autores principales: Patel, Amisha A., McAlinden, Niall, Mathieson, Keith, Sakata, Shuzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047771/
https://www.ncbi.nlm.nih.gov/pubmed/32153363
http://dx.doi.org/10.3389/fnins.2020.00148
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author Patel, Amisha A.
McAlinden, Niall
Mathieson, Keith
Sakata, Shuzo
author_facet Patel, Amisha A.
McAlinden, Niall
Mathieson, Keith
Sakata, Shuzo
author_sort Patel, Amisha A.
collection PubMed
description In vivo electrophysiology is the gold standard technique used to investigate sub-second neural dynamics in freely behaving animals. However, monitoring cell-type-specific population activity is not a trivial task. Over the last decade, fiber photometry based on genetically encoded calcium indicators (GECIs) has been widely adopted as a versatile tool to monitor cell-type-specific population activity in vivo. However, this approach suffers from low temporal resolution. Here, we combine these two approaches to monitor both sub-second field potentials and cell-type-specific population activity in freely behaving mice. By developing an economical custom-made system and constructing a hybrid implant of an electrode and a fiber optic cannula, we simultaneously monitor artifact-free mesopontine field potentials and calcium transients in cholinergic neurons across the sleep-wake cycle. We find that mesopontine cholinergic activity co-occurs with sub-second pontine waves, called P-waves, during rapid eye movement sleep. Given the simplicity of our approach, simultaneous electrophysiological recording and cell-type-specific imaging provides a novel and valuable tool for interrogating state-dependent neural circuit dynamics in vivo.
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spelling pubmed-70477712020-03-09 Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice Patel, Amisha A. McAlinden, Niall Mathieson, Keith Sakata, Shuzo Front Neurosci Neuroscience In vivo electrophysiology is the gold standard technique used to investigate sub-second neural dynamics in freely behaving animals. However, monitoring cell-type-specific population activity is not a trivial task. Over the last decade, fiber photometry based on genetically encoded calcium indicators (GECIs) has been widely adopted as a versatile tool to monitor cell-type-specific population activity in vivo. However, this approach suffers from low temporal resolution. Here, we combine these two approaches to monitor both sub-second field potentials and cell-type-specific population activity in freely behaving mice. By developing an economical custom-made system and constructing a hybrid implant of an electrode and a fiber optic cannula, we simultaneously monitor artifact-free mesopontine field potentials and calcium transients in cholinergic neurons across the sleep-wake cycle. We find that mesopontine cholinergic activity co-occurs with sub-second pontine waves, called P-waves, during rapid eye movement sleep. Given the simplicity of our approach, simultaneous electrophysiological recording and cell-type-specific imaging provides a novel and valuable tool for interrogating state-dependent neural circuit dynamics in vivo. Frontiers Media S.A. 2020-02-21 /pmc/articles/PMC7047771/ /pubmed/32153363 http://dx.doi.org/10.3389/fnins.2020.00148 Text en Copyright © 2020 Patel, McAlinden, Mathieson and Sakata. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Patel, Amisha A.
McAlinden, Niall
Mathieson, Keith
Sakata, Shuzo
Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title_full Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title_fullStr Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title_full_unstemmed Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title_short Simultaneous Electrophysiology and Fiber Photometry in Freely Behaving Mice
title_sort simultaneous electrophysiology and fiber photometry in freely behaving mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047771/
https://www.ncbi.nlm.nih.gov/pubmed/32153363
http://dx.doi.org/10.3389/fnins.2020.00148
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