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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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. |
format | Online Article Text |
id | pubmed-9619307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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