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Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region

A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether fr...

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Autores principales: van der Zouwen, Cornelis Immanuel, Boutin, Joël, Fougère, Maxime, Flaive, Aurélie, Vivancos, Mélanie, Santuz, Alessandro, Akay, Turgay, Sarret, Philippe, Ryczko, Dimitri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062873/
https://www.ncbi.nlm.nih.gov/pubmed/33897379
http://dx.doi.org/10.3389/fncir.2021.639900
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author van der Zouwen, Cornelis Immanuel
Boutin, Joël
Fougère, Maxime
Flaive, Aurélie
Vivancos, Mélanie
Santuz, Alessandro
Akay, Turgay
Sarret, Philippe
Ryczko, Dimitri
author_facet van der Zouwen, Cornelis Immanuel
Boutin, Joël
Fougère, Maxime
Flaive, Aurélie
Vivancos, Mélanie
Santuz, Alessandro
Akay, Turgay
Sarret, Philippe
Ryczko, Dimitri
author_sort van der Zouwen, Cornelis Immanuel
collection PubMed
description A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether freely behaving mice could brake or turn, based on environmental cues during MLR stimulation. We photostimulated the cuneiform nucleus (part of the MLR) in mice expressing channelrhodopsin in Vglut2-positive neurons in a Cre-dependent manner (Vglut2-ChR2-EYFP) using optogenetics. We detected locomotor movements using deep learning. We used patch-clamp recordings to validate the functional expression of channelrhodopsin and neuroanatomy to visualize the stimulation sites. In the linear corridor, gait diagram and limb kinematics were similar during spontaneous and optogenetic-evoked locomotion. In the open-field arena, optogenetic stimulation of the MLR evoked locomotion, and increasing laser power increased locomotor speed. Mice could brake and make sharp turns (~90°) when approaching a corner during MLR stimulation in the open-field arena. The speed during the turn was scaled with the speed before the turn, and with the turn angle. Patch-clamp recordings in Vglut2-ChR2-EYFP mice show that blue light evoked short-latency spiking in MLR neurons. Our results strengthen the idea that different brainstem neurons convey braking/turning and MLR speed commands in mammals. Our study also shows that Vglut2-positive neurons of the cuneiform nucleus are a relevant target to increase locomotor activity without impeding the ability to brake and turn when approaching obstacles, thus ensuring smooth and adaptable navigation. Our observations may have clinical relevance since cuneiform nucleus stimulation is increasingly considered to improve locomotion function in pathological states such as Parkinson’s disease, spinal cord injury, or stroke.
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spelling pubmed-80628732021-04-24 Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region van der Zouwen, Cornelis Immanuel Boutin, Joël Fougère, Maxime Flaive, Aurélie Vivancos, Mélanie Santuz, Alessandro Akay, Turgay Sarret, Philippe Ryczko, Dimitri Front Neural Circuits Neuroscience A key function of the mesencephalic locomotor region (MLR) is to control the speed of forward symmetrical locomotor movements. However, the ability of freely moving mammals to integrate environmental cues to brake and turn during MLR stimulation is poorly documented. Here, we investigated whether freely behaving mice could brake or turn, based on environmental cues during MLR stimulation. We photostimulated the cuneiform nucleus (part of the MLR) in mice expressing channelrhodopsin in Vglut2-positive neurons in a Cre-dependent manner (Vglut2-ChR2-EYFP) using optogenetics. We detected locomotor movements using deep learning. We used patch-clamp recordings to validate the functional expression of channelrhodopsin and neuroanatomy to visualize the stimulation sites. In the linear corridor, gait diagram and limb kinematics were similar during spontaneous and optogenetic-evoked locomotion. In the open-field arena, optogenetic stimulation of the MLR evoked locomotion, and increasing laser power increased locomotor speed. Mice could brake and make sharp turns (~90°) when approaching a corner during MLR stimulation in the open-field arena. The speed during the turn was scaled with the speed before the turn, and with the turn angle. Patch-clamp recordings in Vglut2-ChR2-EYFP mice show that blue light evoked short-latency spiking in MLR neurons. Our results strengthen the idea that different brainstem neurons convey braking/turning and MLR speed commands in mammals. Our study also shows that Vglut2-positive neurons of the cuneiform nucleus are a relevant target to increase locomotor activity without impeding the ability to brake and turn when approaching obstacles, thus ensuring smooth and adaptable navigation. Our observations may have clinical relevance since cuneiform nucleus stimulation is increasingly considered to improve locomotion function in pathological states such as Parkinson’s disease, spinal cord injury, or stroke. Frontiers Media S.A. 2021-04-09 /pmc/articles/PMC8062873/ /pubmed/33897379 http://dx.doi.org/10.3389/fncir.2021.639900 Text en Copyright © 2021 van der Zouwen, Boutin, Fougère, Flaive, Vivancos, Santuz, Akay, Sarret and Ryczko. https://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
van der Zouwen, Cornelis Immanuel
Boutin, Joël
Fougère, Maxime
Flaive, Aurélie
Vivancos, Mélanie
Santuz, Alessandro
Akay, Turgay
Sarret, Philippe
Ryczko, Dimitri
Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title_full Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title_fullStr Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title_full_unstemmed Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title_short Freely Behaving Mice Can Brake and Turn During Optogenetic Stimulation of the Mesencephalic Locomotor Region
title_sort freely behaving mice can brake and turn during optogenetic stimulation of the mesencephalic locomotor region
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062873/
https://www.ncbi.nlm.nih.gov/pubmed/33897379
http://dx.doi.org/10.3389/fncir.2021.639900
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