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Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour
The pivotal role of the periaqueductal grey (PAG) in fear learning is reinforced by the identification of neurons in male rat ventrolateral PAG (vlPAG) that encode fear memory through signalling the onset and offset of an auditory-conditioned stimulus during presentation of the unreinforced conditio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923669/ https://www.ncbi.nlm.nih.gov/pubmed/35287795 http://dx.doi.org/10.7554/eLife.76278 |
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author | Lawrenson, Charlotte Paci, Elena Pickford, Jasmine Drake, Robert AR Lumb, Bridget M Apps, Richard |
author_facet | Lawrenson, Charlotte Paci, Elena Pickford, Jasmine Drake, Robert AR Lumb, Bridget M Apps, Richard |
author_sort | Lawrenson, Charlotte |
collection | PubMed |
description | The pivotal role of the periaqueductal grey (PAG) in fear learning is reinforced by the identification of neurons in male rat ventrolateral PAG (vlPAG) that encode fear memory through signalling the onset and offset of an auditory-conditioned stimulus during presentation of the unreinforced conditioned tone (CS+) during retrieval. Some units only display CS+ onset or offset responses, and the two signals differ in extinction sensitivity, suggesting that they are independent of each other. In addition, understanding cerebellar contributions to survival circuits is advanced by the discovery that (i) reversible inactivation of the medial cerebellar nucleus (MCN) during fear consolidation leads in subsequent retrieval to (a) disruption of the temporal precision of vlPAG offset, but not onset responses to CS+, and (b) an increase in duration of freezing behaviour. And (ii) chemogenetic manipulation of the MCN-vlPAG projection during fear acquisition (a) reduces the occurrence of fear-related ultrasonic vocalisations, and (b) during subsequent retrieval, slows the extinction rate of fear-related freezing. These findings show that the cerebellum is part of the survival network that regulates fear memory processes at multiple timescales and in multiple ways, raising the possibility that dysfunctional interactions in the cerebellar-survival network may underlie fear-related disorders and comorbidities. |
format | Online Article Text |
id | pubmed-8923669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-89236692022-03-16 Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour Lawrenson, Charlotte Paci, Elena Pickford, Jasmine Drake, Robert AR Lumb, Bridget M Apps, Richard eLife Neuroscience The pivotal role of the periaqueductal grey (PAG) in fear learning is reinforced by the identification of neurons in male rat ventrolateral PAG (vlPAG) that encode fear memory through signalling the onset and offset of an auditory-conditioned stimulus during presentation of the unreinforced conditioned tone (CS+) during retrieval. Some units only display CS+ onset or offset responses, and the two signals differ in extinction sensitivity, suggesting that they are independent of each other. In addition, understanding cerebellar contributions to survival circuits is advanced by the discovery that (i) reversible inactivation of the medial cerebellar nucleus (MCN) during fear consolidation leads in subsequent retrieval to (a) disruption of the temporal precision of vlPAG offset, but not onset responses to CS+, and (b) an increase in duration of freezing behaviour. And (ii) chemogenetic manipulation of the MCN-vlPAG projection during fear acquisition (a) reduces the occurrence of fear-related ultrasonic vocalisations, and (b) during subsequent retrieval, slows the extinction rate of fear-related freezing. These findings show that the cerebellum is part of the survival network that regulates fear memory processes at multiple timescales and in multiple ways, raising the possibility that dysfunctional interactions in the cerebellar-survival network may underlie fear-related disorders and comorbidities. eLife Sciences Publications, Ltd 2022-03-15 /pmc/articles/PMC8923669/ /pubmed/35287795 http://dx.doi.org/10.7554/eLife.76278 Text en © 2022, Lawrenson, Paci et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Lawrenson, Charlotte Paci, Elena Pickford, Jasmine Drake, Robert AR Lumb, Bridget M Apps, Richard Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title | Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title_full | Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title_fullStr | Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title_full_unstemmed | Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title_short | Cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
title_sort | cerebellar modulation of memory encoding in the periaqueductal grey and fear behaviour |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923669/ https://www.ncbi.nlm.nih.gov/pubmed/35287795 http://dx.doi.org/10.7554/eLife.76278 |
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