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Cerebellar contribution to threat probability in a SCA6 mouse model
Fear and anxiety have proven to be essential during the evolutionary process. However, the mechanisms involved in recognizing and categorizing threat probability (i.e. low to high) to elicit the appropriate defensive behavior are yet to be determined. In this study, we investigated the cerebellar co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652111/ https://www.ncbi.nlm.nih.gov/pubmed/35708512 http://dx.doi.org/10.1093/hmg/ddac135 |
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author | Bohne, Pauline Rybarski, Max Mourabit, Damian Boden-El Krause, Felix Mark, Melanie D |
author_facet | Bohne, Pauline Rybarski, Max Mourabit, Damian Boden-El Krause, Felix Mark, Melanie D |
author_sort | Bohne, Pauline |
collection | PubMed |
description | Fear and anxiety have proven to be essential during the evolutionary process. However, the mechanisms involved in recognizing and categorizing threat probability (i.e. low to high) to elicit the appropriate defensive behavior are yet to be determined. In this study, we investigated the cerebellar contribution in evoking appropriate defensive escape behavior using a purely cerebellar, neurodegenerative mouse model for spinocerebellar ataxia type 6 which is caused by an expanded CAG repeat in exon 47 of the P/Q type calcium channel α1A subunit. These mice overexpress the carboxy terminus (CT) of the P/Q type calcium channel containing an expanded 27 CAG repeat specifically in cerebellar Purkinje cells (CT-longQ27(PC)). We found that our CT-longQ27(PC) mice exhibit anxiolytic behavior in the open field, elevated plus maze and light/dark place preference tests, which could be recovered with more threatening conditions such as brighter lighting, meowing sounds and an ultrasound repellent. Their innate fear to find safety in the Barnes maze and visual cliff tests was also diminished with subsequent trials, which could be partially recovered with an ultrasound repellent in the Barnes maze. However, under higher threat conditions such as in the light/dark place preference with ultrasound repellent and in the looming tests, CT-longQ27(PC) mice responded with higher defensive escape behaviors as controls. Moreover, CT-longQ27(PC) mice displayed increased levels of CT-labeled aggregates compared with controls. Together these data suggest that cerebellar degeneration by overexpression of CT-longQ27(PC) is sufficient to impair defensive escape responses in those mice. |
format | Online Article Text |
id | pubmed-9652111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96521112022-11-14 Cerebellar contribution to threat probability in a SCA6 mouse model Bohne, Pauline Rybarski, Max Mourabit, Damian Boden-El Krause, Felix Mark, Melanie D Hum Mol Genet Original Article Fear and anxiety have proven to be essential during the evolutionary process. However, the mechanisms involved in recognizing and categorizing threat probability (i.e. low to high) to elicit the appropriate defensive behavior are yet to be determined. In this study, we investigated the cerebellar contribution in evoking appropriate defensive escape behavior using a purely cerebellar, neurodegenerative mouse model for spinocerebellar ataxia type 6 which is caused by an expanded CAG repeat in exon 47 of the P/Q type calcium channel α1A subunit. These mice overexpress the carboxy terminus (CT) of the P/Q type calcium channel containing an expanded 27 CAG repeat specifically in cerebellar Purkinje cells (CT-longQ27(PC)). We found that our CT-longQ27(PC) mice exhibit anxiolytic behavior in the open field, elevated plus maze and light/dark place preference tests, which could be recovered with more threatening conditions such as brighter lighting, meowing sounds and an ultrasound repellent. Their innate fear to find safety in the Barnes maze and visual cliff tests was also diminished with subsequent trials, which could be partially recovered with an ultrasound repellent in the Barnes maze. However, under higher threat conditions such as in the light/dark place preference with ultrasound repellent and in the looming tests, CT-longQ27(PC) mice responded with higher defensive escape behaviors as controls. Moreover, CT-longQ27(PC) mice displayed increased levels of CT-labeled aggregates compared with controls. Together these data suggest that cerebellar degeneration by overexpression of CT-longQ27(PC) is sufficient to impair defensive escape responses in those mice. Oxford University Press 2022-06-16 /pmc/articles/PMC9652111/ /pubmed/35708512 http://dx.doi.org/10.1093/hmg/ddac135 Text en © The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Bohne, Pauline Rybarski, Max Mourabit, Damian Boden-El Krause, Felix Mark, Melanie D Cerebellar contribution to threat probability in a SCA6 mouse model |
title | Cerebellar contribution to threat probability in a SCA6 mouse model |
title_full | Cerebellar contribution to threat probability in a SCA6 mouse model |
title_fullStr | Cerebellar contribution to threat probability in a SCA6 mouse model |
title_full_unstemmed | Cerebellar contribution to threat probability in a SCA6 mouse model |
title_short | Cerebellar contribution to threat probability in a SCA6 mouse model |
title_sort | cerebellar contribution to threat probability in a sca6 mouse model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652111/ https://www.ncbi.nlm.nih.gov/pubmed/35708512 http://dx.doi.org/10.1093/hmg/ddac135 |
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