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Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice
The optokinetic response (OKR), a reflexive eye movement evoked by a motion of the visual field, is known to adapt its strength to cope with an environmental change throughout life, which is a type of cerebellum-dependent learning. Previous studies suggested that OKR learning induces changes in in-v...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542746/ https://www.ncbi.nlm.nih.gov/pubmed/33028375 http://dx.doi.org/10.1186/s13041-020-00678-2 |
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author | Kim, Yong Gyu Kim, Sang Jeong |
author_facet | Kim, Yong Gyu Kim, Sang Jeong |
author_sort | Kim, Yong Gyu |
collection | PubMed |
description | The optokinetic response (OKR), a reflexive eye movement evoked by a motion of the visual field, is known to adapt its strength to cope with an environmental change throughout life, which is a type of cerebellum-dependent learning. Previous studies suggested that OKR learning induces changes in in-vivo spiking activity and synaptic transmission of the cerebellar Purkinje cell (PC). Despite the recent emphasis on the importance of the intrinsic excitability related to learning and memory, the direct correlation between the intrinsic excitability of PCs and OKR learning has not been tested. In the present study, by utilizing the whole-cell patch-clamp recording, we compared the responses of cerebellar PCs to somatic current injection between the control and learned groups. We found that the neurons from the learned group showed a significant reduction in mean firing rate compared with neurons in the control group. In the analysis of single action potential (AP), we revealed that the rheobase current for the generation of single AP was increased by OKR learning, while AP threshold, AP amplitude, and afterhyperpolarization amplitude were not altered. Taken together, our result suggests that the decrease in the intrinsic excitability was induced in the cerebellar PC of learned group by an increase in the current threshold for generating AP. |
format | Online Article Text |
id | pubmed-7542746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75427462020-10-08 Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice Kim, Yong Gyu Kim, Sang Jeong Mol Brain Micro Report The optokinetic response (OKR), a reflexive eye movement evoked by a motion of the visual field, is known to adapt its strength to cope with an environmental change throughout life, which is a type of cerebellum-dependent learning. Previous studies suggested that OKR learning induces changes in in-vivo spiking activity and synaptic transmission of the cerebellar Purkinje cell (PC). Despite the recent emphasis on the importance of the intrinsic excitability related to learning and memory, the direct correlation between the intrinsic excitability of PCs and OKR learning has not been tested. In the present study, by utilizing the whole-cell patch-clamp recording, we compared the responses of cerebellar PCs to somatic current injection between the control and learned groups. We found that the neurons from the learned group showed a significant reduction in mean firing rate compared with neurons in the control group. In the analysis of single action potential (AP), we revealed that the rheobase current for the generation of single AP was increased by OKR learning, while AP threshold, AP amplitude, and afterhyperpolarization amplitude were not altered. Taken together, our result suggests that the decrease in the intrinsic excitability was induced in the cerebellar PC of learned group by an increase in the current threshold for generating AP. BioMed Central 2020-10-07 /pmc/articles/PMC7542746/ /pubmed/33028375 http://dx.doi.org/10.1186/s13041-020-00678-2 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Micro Report Kim, Yong Gyu Kim, Sang Jeong Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title | Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title_full | Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title_fullStr | Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title_full_unstemmed | Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title_short | Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice |
title_sort | decreased intrinsic excitability of cerebellar purkinje cells following optokinetic learning in mice |
topic | Micro Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542746/ https://www.ncbi.nlm.nih.gov/pubmed/33028375 http://dx.doi.org/10.1186/s13041-020-00678-2 |
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