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Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium

Experience-dependent brain circuit plasticity underlies various sensorimotor learning and memory processes. Recently, a novel set-point adaptation mechanism was identified that accounts for the pronounced negative optokinetic afternystagmus (OKAN) following a sustained period of unidirectional optok...

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Autores principales: Lin, Ting-Feng, Mohammadi, Mohammad, Cullen, Kathleen E., Chacron, Maurice J., Huang, Melody Ying-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619307/
https://www.ncbi.nlm.nih.gov/pubmed/36325052
http://dx.doi.org/10.1016/j.isci.2022.105335
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author Lin, Ting-Feng
Mohammadi, Mohammad
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
author_facet Lin, Ting-Feng
Mohammadi, Mohammad
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
author_sort Lin, Ting-Feng
collection PubMed
description Experience-dependent brain circuit plasticity underlies various sensorimotor learning and memory processes. Recently, a novel set-point adaptation mechanism was identified that accounts for the pronounced negative optokinetic afternystagmus (OKAN) following a sustained period of unidirectional optokinetic nystagmus (OKN) in larval zebrafish. To investigate the physiological significance of optokinetic set-point adaptation, animals in the current study were exposed to a direction-alternating optokinetic stimulation paradigm that better resembles their visual experience in nature. Our results reveal that not only was asymmetric alternating stimulation sufficient to induce the set-point adaptation and the resulting negative OKAN, but most strikingly, under symmetric alternating stimulation some animals displayed an inherent bias of the OKN gain in one direction, and that was compensated by the similar set-point adaptation. This finding, supported by mathematical modeling, suggests that set-point adaptation allows animals to cope with asymmetric optokinetic behaviors evoked by either external stimuli or innate oculomotor biases.
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spelling pubmed-96193072022-11-01 Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium Lin, Ting-Feng Mohammadi, Mohammad Cullen, Kathleen E. Chacron, Maurice J. Huang, Melody Ying-Yu iScience Article Experience-dependent brain circuit plasticity underlies various sensorimotor learning and memory processes. Recently, a novel set-point adaptation mechanism was identified that accounts for the pronounced negative optokinetic afternystagmus (OKAN) following a sustained period of unidirectional optokinetic nystagmus (OKN) in larval zebrafish. To investigate the physiological significance of optokinetic set-point adaptation, animals in the current study were exposed to a direction-alternating optokinetic stimulation paradigm that better resembles their visual experience in nature. Our results reveal that not only was asymmetric alternating stimulation sufficient to induce the set-point adaptation and the resulting negative OKAN, but most strikingly, under symmetric alternating stimulation some animals displayed an inherent bias of the OKN gain in one direction, and that was compensated by the similar set-point adaptation. This finding, supported by mathematical modeling, suggests that set-point adaptation allows animals to cope with asymmetric optokinetic behaviors evoked by either external stimuli or innate oculomotor biases. Elsevier 2022-10-12 /pmc/articles/PMC9619307/ /pubmed/36325052 http://dx.doi.org/10.1016/j.isci.2022.105335 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Lin, Ting-Feng
Mohammadi, Mohammad
Cullen, Kathleen E.
Chacron, Maurice J.
Huang, Melody Ying-Yu
Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title_full Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title_fullStr Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title_full_unstemmed Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title_short Optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
title_sort optokinetic set-point adaptation functions as an internal dynamic calibration mechanism for oculomotor disequilibrium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9619307/
https://www.ncbi.nlm.nih.gov/pubmed/36325052
http://dx.doi.org/10.1016/j.isci.2022.105335
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