Cholinergic modulation of sensory processing in awake mouse cortex

Abstract Cholinergic modulation of brain activity is fundamental for awareness and conscious sensorimotor behaviours, but deciphering the timing and significance of acetylcholine actions for these behaviours is challenging. The widespread nature of cholinergic projections to the cortex means that ne...

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Main Authors: Javier Jimenez-Martin, Daniil Potapov, Kay Potapov, Thomas Knöpfel, Ruth M. Empson
Format: Article
Language:English
Published: Nature Publishing Group 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-96696-8
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spelling doaj-73730454205d4df7a402ff43b1062d0f2021-09-05T11:31:20ZengNature Publishing GroupScientific Reports2045-23222021-09-0111112010.1038/s41598-021-96696-8Cholinergic modulation of sensory processing in awake mouse cortexJavier Jimenez-Martin0Daniil Potapov1Kay Potapov2Thomas Knöpfel3Ruth M. Empson4Department of Physiology, Biomedical Sciences, Brain Health Research Centre and Brain Research NZ, University of OtagoDepartment of Physiology, Biomedical Sciences, Brain Health Research Centre and Brain Research NZ, University of OtagoDepartment of Physiology, Biomedical Sciences, Brain Health Research Centre and Brain Research NZ, University of OtagoFaculty of Medicine, Department of Brain Sciences, Imperial College LondonDepartment of Physiology, Biomedical Sciences, Brain Health Research Centre and Brain Research NZ, University of OtagoAbstract Cholinergic modulation of brain activity is fundamental for awareness and conscious sensorimotor behaviours, but deciphering the timing and significance of acetylcholine actions for these behaviours is challenging. The widespread nature of cholinergic projections to the cortex means that new insights require access to specific neuronal populations, and on a time-scale that matches behaviourally relevant cholinergic actions. Here, we use fast, voltage imaging of L2/3 cortical pyramidal neurons exclusively expressing the genetically-encoded voltage indicator Butterfly 1.2, in awake, head-fixed mice, receiving sensory stimulation, whilst manipulating the cholinergic system. Altering muscarinic acetylcholine function re-shaped sensory-evoked fast depolarisation and subsequent slow hyperpolarisation of L2/3 pyramidal neurons. A consequence of this re-shaping was disrupted adaptation of the sensory-evoked responses, suggesting a critical role for acetylcholine during sensory discrimination behaviour. Our findings provide new insights into how the cortex processes sensory information and how loss of acetylcholine, for example in Alzheimer’s Disease, disrupts sensory behaviours.https://doi.org/10.1038/s41598-021-96696-8
collection DOAJ
language English
format Article
sources DOAJ
author Javier Jimenez-Martin
Daniil Potapov
Kay Potapov
Thomas Knöpfel
Ruth M. Empson
spellingShingle Javier Jimenez-Martin
Daniil Potapov
Kay Potapov
Thomas Knöpfel
Ruth M. Empson
Cholinergic modulation of sensory processing in awake mouse cortex
Scientific Reports
author_facet Javier Jimenez-Martin
Daniil Potapov
Kay Potapov
Thomas Knöpfel
Ruth M. Empson
author_sort Javier Jimenez-Martin
title Cholinergic modulation of sensory processing in awake mouse cortex
title_short Cholinergic modulation of sensory processing in awake mouse cortex
title_full Cholinergic modulation of sensory processing in awake mouse cortex
title_fullStr Cholinergic modulation of sensory processing in awake mouse cortex
title_full_unstemmed Cholinergic modulation of sensory processing in awake mouse cortex
title_sort cholinergic modulation of sensory processing in awake mouse cortex
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-09-01
description Abstract Cholinergic modulation of brain activity is fundamental for awareness and conscious sensorimotor behaviours, but deciphering the timing and significance of acetylcholine actions for these behaviours is challenging. The widespread nature of cholinergic projections to the cortex means that new insights require access to specific neuronal populations, and on a time-scale that matches behaviourally relevant cholinergic actions. Here, we use fast, voltage imaging of L2/3 cortical pyramidal neurons exclusively expressing the genetically-encoded voltage indicator Butterfly 1.2, in awake, head-fixed mice, receiving sensory stimulation, whilst manipulating the cholinergic system. Altering muscarinic acetylcholine function re-shaped sensory-evoked fast depolarisation and subsequent slow hyperpolarisation of L2/3 pyramidal neurons. A consequence of this re-shaping was disrupted adaptation of the sensory-evoked responses, suggesting a critical role for acetylcholine during sensory discrimination behaviour. Our findings provide new insights into how the cortex processes sensory information and how loss of acetylcholine, for example in Alzheimer’s Disease, disrupts sensory behaviours.
url https://doi.org/10.1038/s41598-021-96696-8
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