Cargando…

Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus

In larval xenopus, locomotor-induced oculomotor behavior produces gaze-stabilizing eye movements to counteract the disruptive effects of tail undulation during swimming. While neuronal circuitries responsible for feed-forward intrinsic spino-extraocular signaling have recently been described, the re...

Descripción completa

Detalles Bibliográficos
Autores principales: Bacqué-Cazenave, Julien, Courtand, Gilles, Beraneck, Mathieu, Lambert, François M., Combes, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216112/
https://www.ncbi.nlm.nih.gov/pubmed/30420798
http://dx.doi.org/10.3389/fncir.2018.00095
_version_ 1783368283841363968
author Bacqué-Cazenave, Julien
Courtand, Gilles
Beraneck, Mathieu
Lambert, François M.
Combes, Denis
author_facet Bacqué-Cazenave, Julien
Courtand, Gilles
Beraneck, Mathieu
Lambert, François M.
Combes, Denis
author_sort Bacqué-Cazenave, Julien
collection PubMed
description In larval xenopus, locomotor-induced oculomotor behavior produces gaze-stabilizing eye movements to counteract the disruptive effects of tail undulation during swimming. While neuronal circuitries responsible for feed-forward intrinsic spino-extraocular signaling have recently been described, the resulting oculomotor behavior remains poorly understood. Conveying locomotor CPG efference copy, the spino-extraocular motor command coordinates the multi-segmental rostrocaudal spinal rhythmic activity with the extraocular motor activity. By recording sequences of xenopus tadpole free swimming, we quantified the temporal calibration of conjugate eye movements originating from spino-extraocular motor coupled activity during pre-metamorphic tail-based undulatory swimming. Our results show that eye movements are produced only during robust propulsive forward swimming activity and increase with the amplitude of tail movements. The use of larval isolated in vitro and semi-intact fixed head preparations revealed that spinal locomotor networks driving the rostral portion of the tail set the precise timing of the spino-extraocular motor coupling by adjusting the phase relationship between spinal segment and extraocular rhythmic activity with the swimming frequency. The resulting spinal-evoked oculomotor behavior produced conjugated eye movements that were in phase opposition with the mid-caudal part of the tail. This time adjustment is independent of locomotor activity in the more caudal spinal parts of the tail. Altogether our findings demonstrate that locomotor feed-forward spino-extraocular signaling produce conjugate eye movements that compensate specifically the undulation of the mid-caudal tail during active swimming. Finally, this study constitutes the first extensive behavioral quantification of spino-extraocular motor coupling, which sets the basis for understanding the mechanisms of locomotor-induced oculomotor behavior in larval frog.
format Online
Article
Text
id pubmed-6216112
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62161122018-11-12 Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus Bacqué-Cazenave, Julien Courtand, Gilles Beraneck, Mathieu Lambert, François M. Combes, Denis Front Neural Circuits Neuroscience In larval xenopus, locomotor-induced oculomotor behavior produces gaze-stabilizing eye movements to counteract the disruptive effects of tail undulation during swimming. While neuronal circuitries responsible for feed-forward intrinsic spino-extraocular signaling have recently been described, the resulting oculomotor behavior remains poorly understood. Conveying locomotor CPG efference copy, the spino-extraocular motor command coordinates the multi-segmental rostrocaudal spinal rhythmic activity with the extraocular motor activity. By recording sequences of xenopus tadpole free swimming, we quantified the temporal calibration of conjugate eye movements originating from spino-extraocular motor coupled activity during pre-metamorphic tail-based undulatory swimming. Our results show that eye movements are produced only during robust propulsive forward swimming activity and increase with the amplitude of tail movements. The use of larval isolated in vitro and semi-intact fixed head preparations revealed that spinal locomotor networks driving the rostral portion of the tail set the precise timing of the spino-extraocular motor coupling by adjusting the phase relationship between spinal segment and extraocular rhythmic activity with the swimming frequency. The resulting spinal-evoked oculomotor behavior produced conjugated eye movements that were in phase opposition with the mid-caudal part of the tail. This time adjustment is independent of locomotor activity in the more caudal spinal parts of the tail. Altogether our findings demonstrate that locomotor feed-forward spino-extraocular signaling produce conjugate eye movements that compensate specifically the undulation of the mid-caudal tail during active swimming. Finally, this study constitutes the first extensive behavioral quantification of spino-extraocular motor coupling, which sets the basis for understanding the mechanisms of locomotor-induced oculomotor behavior in larval frog. Frontiers Media S.A. 2018-10-29 /pmc/articles/PMC6216112/ /pubmed/30420798 http://dx.doi.org/10.3389/fncir.2018.00095 Text en Copyright © 2018 Bacqué-Cazenave, Courtand, Beraneck, Lambert and Combes. 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
Bacqué-Cazenave, Julien
Courtand, Gilles
Beraneck, Mathieu
Lambert, François M.
Combes, Denis
Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title_full Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title_fullStr Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title_full_unstemmed Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title_short Temporal Relationship of Ocular and Tail Segmental Movements Underlying Locomotor-Induced Gaze Stabilization During Undulatory Swimming in Larval Xenopus
title_sort temporal relationship of ocular and tail segmental movements underlying locomotor-induced gaze stabilization during undulatory swimming in larval xenopus
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216112/
https://www.ncbi.nlm.nih.gov/pubmed/30420798
http://dx.doi.org/10.3389/fncir.2018.00095
work_keys_str_mv AT bacquecazenavejulien temporalrelationshipofocularandtailsegmentalmovementsunderlyinglocomotorinducedgazestabilizationduringundulatoryswimminginlarvalxenopus
AT courtandgilles temporalrelationshipofocularandtailsegmentalmovementsunderlyinglocomotorinducedgazestabilizationduringundulatoryswimminginlarvalxenopus
AT beraneckmathieu temporalrelationshipofocularandtailsegmentalmovementsunderlyinglocomotorinducedgazestabilizationduringundulatoryswimminginlarvalxenopus
AT lambertfrancoism temporalrelationshipofocularandtailsegmentalmovementsunderlyinglocomotorinducedgazestabilizationduringundulatoryswimminginlarvalxenopus
AT combesdenis temporalrelationshipofocularandtailsegmentalmovementsunderlyinglocomotorinducedgazestabilizationduringundulatoryswimminginlarvalxenopus