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...
Autores principales: | , , , , |
---|---|
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 |