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

ERPs cerebellum dynamic causal modeling (DCM) extinction fear periaqueductal gray

Journal

Frontiers in systems neuroscience
ISSN: 1662-5137
Titre abrégé: Front Syst Neurosci
Pays: Switzerland
ID NLM: 101477946

Informations de publication

Date de publication:
2023
Historique:
received: 20 01 2023
accepted: 12 04 2023
medline: 2 6 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: epublish

Résumé

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. 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. 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. The results are consistent with the cerebellum contributing to predictive processes that underpin fear extinction.

Identifiants

pubmed: 37266394
doi: 10.3389/fnsys.2023.1148604
pmc: PMC10229824
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1148604

Informations de copyright

Copyright © 2023 Paci, Lumb, Apps, Lawrenson and Moran.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Elena Paci (E)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Bridget M Lumb (BM)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Richard Apps (R)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Charlotte L Lawrenson (CL)

School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, United Kingdom.

Rosalyn J Moran (RJ)

Department of Neuroimaging, King's College London, London, United Kingdom.

Classifications MeSH