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Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction

INTRODUCTION: The extinction of fear memories is an important component in regulating defensive behaviors, contributing toward adaptive processes essential for survival. The cerebellar medial nucleus (MCN) has bidirectional connections with the ventrolateral periaqueductal gray (vlPAG) and is implic...

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Autores principales: Paci, Elena, Lumb, Bridget M., Apps, Richard, Lawrenson, Charlotte L., Moran, Rosalyn J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229824/
https://www.ncbi.nlm.nih.gov/pubmed/37266394
http://dx.doi.org/10.3389/fnsys.2023.1148604
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author Paci, Elena
Lumb, Bridget M.
Apps, Richard
Lawrenson, Charlotte L.
Moran, Rosalyn J.
author_facet Paci, Elena
Lumb, Bridget M.
Apps, Richard
Lawrenson, Charlotte L.
Moran, Rosalyn J.
author_sort Paci, Elena
collection PubMed
description INTRODUCTION: The extinction of fear memories is an important component in regulating defensive behaviors, contributing toward adaptive processes essential for survival. The cerebellar medial nucleus (MCN) has bidirectional connections with the ventrolateral periaqueductal gray (vlPAG) and is implicated in the regulation of multiple aspects of fear, such as conditioned fear learning and the expression of defensive motor outputs. However, it is unclear how communication between the MCN and vlPAG changes during conditioned fear extinction. METHODS: We use dynamic causal models (DCMs) to infer effective connectivity between the MCN and vlPAG during auditory cue-conditioned fear retrieval and extinction in the rat. DCMs determine causal relationships between neuronal sources by using neurobiologically motivated models to reproduce the dynamics of post-synaptic potentials generated by synaptic connections within and between brain regions. Auditory event related potentials (ERPs) during the conditioned tone offset were recorded simultaneously from MCN and vlPAG and then modeled to identify changes in the strength of the synaptic inputs between these brain areas and the relationship to freezing behavior across extinction trials. The DCMs were structured to model evoked responses to best represent conditioned tone offset ERPs and were adapted to represent PAG and cerebellar circuitry. RESULTS: With the use of Parametric Empirical Bayesian (PEB) analysis we found that the strength of the information flow, mediated through enhanced synaptic efficacy from MCN to vlPAG was inversely related to freezing during extinction, i.e., communication from MCN to vlPAG increased with extinction. DISCUSSION: The results are consistent with the cerebellum contributing to predictive processes that underpin fear extinction.
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spelling pubmed-102298242023-06-01 Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction Paci, Elena Lumb, Bridget M. Apps, Richard Lawrenson, Charlotte L. Moran, Rosalyn J. Front Syst Neurosci Neuroscience INTRODUCTION: The extinction of fear memories is an important component in regulating defensive behaviors, contributing toward adaptive processes essential for survival. The cerebellar medial nucleus (MCN) has bidirectional connections with the ventrolateral periaqueductal gray (vlPAG) and is implicated in the regulation of multiple aspects of fear, such as conditioned fear learning and the expression of defensive motor outputs. However, it is unclear how communication between the MCN and vlPAG changes during conditioned fear extinction. METHODS: We use dynamic causal models (DCMs) to infer effective connectivity between the MCN and vlPAG during auditory cue-conditioned fear retrieval and extinction in the rat. DCMs determine causal relationships between neuronal sources by using neurobiologically motivated models to reproduce the dynamics of post-synaptic potentials generated by synaptic connections within and between brain regions. Auditory event related potentials (ERPs) during the conditioned tone offset were recorded simultaneously from MCN and vlPAG and then modeled to identify changes in the strength of the synaptic inputs between these brain areas and the relationship to freezing behavior across extinction trials. The DCMs were structured to model evoked responses to best represent conditioned tone offset ERPs and were adapted to represent PAG and cerebellar circuitry. RESULTS: With the use of Parametric Empirical Bayesian (PEB) analysis we found that the strength of the information flow, mediated through enhanced synaptic efficacy from MCN to vlPAG was inversely related to freezing during extinction, i.e., communication from MCN to vlPAG increased with extinction. DISCUSSION: The results are consistent with the cerebellum contributing to predictive processes that underpin fear extinction. Frontiers Media S.A. 2023-05-17 /pmc/articles/PMC10229824/ /pubmed/37266394 http://dx.doi.org/10.3389/fnsys.2023.1148604 Text en Copyright © 2023 Paci, Lumb, Apps, Lawrenson and Moran. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Paci, Elena
Lumb, Bridget M.
Apps, Richard
Lawrenson, Charlotte L.
Moran, Rosalyn J.
Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title_full Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title_fullStr Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title_full_unstemmed Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title_short Dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
title_sort dynamic causal modeling reveals increased cerebellar- periaqueductal gray communication during fear extinction
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229824/
https://www.ncbi.nlm.nih.gov/pubmed/37266394
http://dx.doi.org/10.3389/fnsys.2023.1148604
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