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Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle

Calcium is a critical second messenger in neurons that contributes to learning and memory, but how the coordination of action potentials of neuronal ensembles with the hippocampal local field potential (LFP) is reflected in dynamic calcium activity remains unclear. Here, we recorded hippocampal calc...

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Autores principales: Zhou, Heng, Neville, Kevin R, Goldstein, Nitsan, Kabu, Shushi, Kausar, Naila, Ye, Rong, Nguyen, Thuan Tinh, Gelwan, Noah, Hyman, Bradley T, Gomperts, Stephen N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435325/
https://www.ncbi.nlm.nih.gov/pubmed/30843520
http://dx.doi.org/10.7554/eLife.39777
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author Zhou, Heng
Neville, Kevin R
Goldstein, Nitsan
Kabu, Shushi
Kausar, Naila
Ye, Rong
Nguyen, Thuan Tinh
Gelwan, Noah
Hyman, Bradley T
Gomperts, Stephen N
author_facet Zhou, Heng
Neville, Kevin R
Goldstein, Nitsan
Kabu, Shushi
Kausar, Naila
Ye, Rong
Nguyen, Thuan Tinh
Gelwan, Noah
Hyman, Bradley T
Gomperts, Stephen N
author_sort Zhou, Heng
collection PubMed
description Calcium is a critical second messenger in neurons that contributes to learning and memory, but how the coordination of action potentials of neuronal ensembles with the hippocampal local field potential (LFP) is reflected in dynamic calcium activity remains unclear. Here, we recorded hippocampal calcium activity with endoscopic imaging of the genetically encoded fluorophore GCaMP6 with concomitant LFP in freely behaving mice. Dynamic calcium activity was greater in exploratory behavior and REM sleep than in quiet wakefulness and slow wave sleep, behavioral states that differ with respect to theta and septal cholinergic activity, and modulated at sharp wave ripples (SWRs). Chemogenetic activation of septal cholinergic neurons expressing the excitatory hM3Dq DREADD increased calcium activity and reduced SWRs. Furthermore, inhibition of muscarinic acetylcholine receptors (mAChRs) reduced calcium activity while increasing SWRs. These results demonstrate that hippocampal dynamic calcium activity depends on behavioral and theta state as well as endogenous mAChR activation.
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spelling pubmed-64353252019-03-27 Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle Zhou, Heng Neville, Kevin R Goldstein, Nitsan Kabu, Shushi Kausar, Naila Ye, Rong Nguyen, Thuan Tinh Gelwan, Noah Hyman, Bradley T Gomperts, Stephen N eLife Neuroscience Calcium is a critical second messenger in neurons that contributes to learning and memory, but how the coordination of action potentials of neuronal ensembles with the hippocampal local field potential (LFP) is reflected in dynamic calcium activity remains unclear. Here, we recorded hippocampal calcium activity with endoscopic imaging of the genetically encoded fluorophore GCaMP6 with concomitant LFP in freely behaving mice. Dynamic calcium activity was greater in exploratory behavior and REM sleep than in quiet wakefulness and slow wave sleep, behavioral states that differ with respect to theta and septal cholinergic activity, and modulated at sharp wave ripples (SWRs). Chemogenetic activation of septal cholinergic neurons expressing the excitatory hM3Dq DREADD increased calcium activity and reduced SWRs. Furthermore, inhibition of muscarinic acetylcholine receptors (mAChRs) reduced calcium activity while increasing SWRs. These results demonstrate that hippocampal dynamic calcium activity depends on behavioral and theta state as well as endogenous mAChR activation. eLife Sciences Publications, Ltd 2019-03-07 /pmc/articles/PMC6435325/ /pubmed/30843520 http://dx.doi.org/10.7554/eLife.39777 Text en © 2019, Zhou et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Zhou, Heng
Neville, Kevin R
Goldstein, Nitsan
Kabu, Shushi
Kausar, Naila
Ye, Rong
Nguyen, Thuan Tinh
Gelwan, Noah
Hyman, Bradley T
Gomperts, Stephen N
Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title_full Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title_fullStr Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title_full_unstemmed Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title_short Cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
title_sort cholinergic modulation of hippocampal calcium activity across the sleep-wake cycle
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435325/
https://www.ncbi.nlm.nih.gov/pubmed/30843520
http://dx.doi.org/10.7554/eLife.39777
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