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Cannabinoids modulate associative cerebellar learning via alterations in behavioral state
Cannabinoids are notorious and profound modulators of behavioral state. In the brain, endocannabinoids act via Type 1-cannabinoid receptors (CB1) to modulate synaptic transmission and mediate multiple forms of synaptic plasticity. CB1 knockout (CB1KO) mice display a range of behavioral phenotypes, i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575324/ https://www.ncbi.nlm.nih.gov/pubmed/33077026 http://dx.doi.org/10.7554/eLife.61821 |
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author | Albergaria, Catarina Silva, N Tatiana Darmohray, Dana M Carey, Megan R |
author_facet | Albergaria, Catarina Silva, N Tatiana Darmohray, Dana M Carey, Megan R |
author_sort | Albergaria, Catarina |
collection | PubMed |
description | Cannabinoids are notorious and profound modulators of behavioral state. In the brain, endocannabinoids act via Type 1-cannabinoid receptors (CB1) to modulate synaptic transmission and mediate multiple forms of synaptic plasticity. CB1 knockout (CB1KO) mice display a range of behavioral phenotypes, in particular hypoactivity and various deficits in learning and memory, including cerebellum-dependent delay eyeblink conditioning. Here we find that the apparent effects of CB1 deletion on cerebellar learning are not due to direct effects on CB1-dependent plasticity, but rather, arise as a secondary consequence of altered behavioral state. Hypoactivity of CB1KO mice accounts for their impaired eyeblink conditioning across both animals and trials. Moreover, learning in these mutants is rescued by walking on a motorized treadmill during training. Finally, cerebellar granule-cell-specific CB1KOs exhibit normal eyeblink conditioning, and both global and granule-cell-specific CB1KOs display normal cerebellum-dependent locomotor coordination and learning. These findings highlight the modulation of behavioral state as a powerful independent means through which individual genes contribute to complex behaviors. |
format | Online Article Text |
id | pubmed-7575324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75753242020-10-21 Cannabinoids modulate associative cerebellar learning via alterations in behavioral state Albergaria, Catarina Silva, N Tatiana Darmohray, Dana M Carey, Megan R eLife Neuroscience Cannabinoids are notorious and profound modulators of behavioral state. In the brain, endocannabinoids act via Type 1-cannabinoid receptors (CB1) to modulate synaptic transmission and mediate multiple forms of synaptic plasticity. CB1 knockout (CB1KO) mice display a range of behavioral phenotypes, in particular hypoactivity and various deficits in learning and memory, including cerebellum-dependent delay eyeblink conditioning. Here we find that the apparent effects of CB1 deletion on cerebellar learning are not due to direct effects on CB1-dependent plasticity, but rather, arise as a secondary consequence of altered behavioral state. Hypoactivity of CB1KO mice accounts for their impaired eyeblink conditioning across both animals and trials. Moreover, learning in these mutants is rescued by walking on a motorized treadmill during training. Finally, cerebellar granule-cell-specific CB1KOs exhibit normal eyeblink conditioning, and both global and granule-cell-specific CB1KOs display normal cerebellum-dependent locomotor coordination and learning. These findings highlight the modulation of behavioral state as a powerful independent means through which individual genes contribute to complex behaviors. eLife Sciences Publications, Ltd 2020-10-20 /pmc/articles/PMC7575324/ /pubmed/33077026 http://dx.doi.org/10.7554/eLife.61821 Text en © 2020, Albergaria et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Albergaria, Catarina Silva, N Tatiana Darmohray, Dana M Carey, Megan R Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title | Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title_full | Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title_fullStr | Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title_full_unstemmed | Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title_short | Cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
title_sort | cannabinoids modulate associative cerebellar learning via alterations in behavioral state |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575324/ https://www.ncbi.nlm.nih.gov/pubmed/33077026 http://dx.doi.org/10.7554/eLife.61821 |
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