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Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation

Motor learning is essential to maintain accurate behavioral responses. We used a larval zebrafish model to study ocular motor learning behaviors. During a sustained period of optokinetic stimulation in 5-day-old wild-type zebrafish larvae the slow-phase eye velocity decreased over time. Then interes...

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Autores principales: Lin, Ting-Feng, Mohammadi, Mohammad, Fathalla, Ahmed M., Pul, Duygu, Lüthi, Dennis, Romano, Fausto, Straumann, Dominik, Cullen, Kathleen E., Chacron, Maurice J., Huang, Melody Ying-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910917/
https://www.ncbi.nlm.nih.gov/pubmed/31836778
http://dx.doi.org/10.1038/s41598-019-55457-4
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author Lin, Ting-Feng
Mohammadi, Mohammad
Fathalla, Ahmed M.
Pul, Duygu
Lüthi, Dennis
Romano, Fausto
Straumann, Dominik
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
author_facet Lin, Ting-Feng
Mohammadi, Mohammad
Fathalla, Ahmed M.
Pul, Duygu
Lüthi, Dennis
Romano, Fausto
Straumann, Dominik
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
author_sort Lin, Ting-Feng
collection PubMed
description Motor learning is essential to maintain accurate behavioral responses. We used a larval zebrafish model to study ocular motor learning behaviors. During a sustained period of optokinetic stimulation in 5-day-old wild-type zebrafish larvae the slow-phase eye velocity decreased over time. Then interestingly, a long-lasting and robust negative optokinetic afternystagmus (OKAN) was evoked upon light extinction. The slow-phase velocity, the quick-phase frequency, and the decay time constant of the negative OKAN were dependent on the stimulus duration and the adaptation to the preceding optokinetic stimulation. Based on these results, we propose a sensory adaptation process during continued optokinetic stimulation, which, when the stimulus is removed, leads to a negative OKAN as the result of a changed retinal slip velocity set point, and thus, a sensorimotor memory. The pronounced negative OKAN in larval zebrafish not only provides a practical solution to the hitherto unsolved problems of observing negative OKAN, but also, and most importantly, can be readily applied as a powerful model for studying sensorimotor learning and memory in vertebrates.
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spelling pubmed-69109172019-12-16 Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation Lin, Ting-Feng Mohammadi, Mohammad Fathalla, Ahmed M. Pul, Duygu Lüthi, Dennis Romano, Fausto Straumann, Dominik Cullen, Kathleen E. Chacron, Maurice J. Huang, Melody Ying-Yu Sci Rep Article Motor learning is essential to maintain accurate behavioral responses. We used a larval zebrafish model to study ocular motor learning behaviors. During a sustained period of optokinetic stimulation in 5-day-old wild-type zebrafish larvae the slow-phase eye velocity decreased over time. Then interestingly, a long-lasting and robust negative optokinetic afternystagmus (OKAN) was evoked upon light extinction. The slow-phase velocity, the quick-phase frequency, and the decay time constant of the negative OKAN were dependent on the stimulus duration and the adaptation to the preceding optokinetic stimulation. Based on these results, we propose a sensory adaptation process during continued optokinetic stimulation, which, when the stimulus is removed, leads to a negative OKAN as the result of a changed retinal slip velocity set point, and thus, a sensorimotor memory. The pronounced negative OKAN in larval zebrafish not only provides a practical solution to the hitherto unsolved problems of observing negative OKAN, but also, and most importantly, can be readily applied as a powerful model for studying sensorimotor learning and memory in vertebrates. Nature Publishing Group UK 2019-12-13 /pmc/articles/PMC6910917/ /pubmed/31836778 http://dx.doi.org/10.1038/s41598-019-55457-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Ting-Feng
Mohammadi, Mohammad
Fathalla, Ahmed M.
Pul, Duygu
Lüthi, Dennis
Romano, Fausto
Straumann, Dominik
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title_full Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title_fullStr Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title_full_unstemmed Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title_short Negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
title_sort negative optokinetic afternystagmus in larval zebrafish demonstrates set-point adaptation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910917/
https://www.ncbi.nlm.nih.gov/pubmed/31836778
http://dx.doi.org/10.1038/s41598-019-55457-4
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