Modulation of 7 T fMRI Signal in the Cerebellar Cortex and Nuclei During Acquisition, Extinction, and Reacquisition of Conditioned Eyeblink Responses

Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster tha...

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Published inHuman brain mapping Vol. 38; no. 8; pp. 3957 - 3974
Main Authors Ernst, Thomas M., Thürling, Markus, Müller, Sarah, Kahl, Fabian, Maderwald, Stefan, Schlamann, Marc, Boele, Henk‐Jan, Koekkoek, Sebastiaan K. E., Diedrichsen, Jörn, De Zeeuw, Chris I., Ladd, Mark E., Timmann, Dagmar
Format Journal Article
LanguageEnglish
Published United States John Wiley & Sons, Inc 01.08.2017
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN1065-9471
1097-0193
1097-0193
DOI10.1002/hbm.23641

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Abstract Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957–3974, 2017. © 2017 Wiley Periodicals, Inc.
AbstractList Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957–3974, 2017 . © 2017 Wiley Periodicals, Inc.
Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957–3974, 2017. © 2017 Wiley Periodicals, Inc.
Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition-related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus-only trials. First-level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957-3974, 2017. © 2017 Wiley Periodicals, Inc.Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition-related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus-only trials. First-level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957-3974, 2017. © 2017 Wiley Periodicals, Inc.
Author Thürling, Markus
Schlamann, Marc
De Zeeuw, Chris I.
Ladd, Mark E.
Koekkoek, Sebastiaan K. E.
Kahl, Fabian
Boele, Henk‐Jan
Timmann, Dagmar
Müller, Sarah
Diedrichsen, Jörn
Ernst, Thomas M.
Maderwald, Stefan
AuthorAffiliation 6 Department for Computer Science University of Western Ontario London Ontario Canada
5 Department of Neuroscience Erasmus MC Rotterdam The Netherlands
1 Department of Neurology Essen University Hospital Essen Germany
4 Department of Neuroradiology University Hospital of Giessen, Justus‐Liebig‐University of Giessen Giessen Germany
3 Department for Diagnostic and Interventional Radiology and Neuroradiology Essen University Hospital, University of Duisburg‐Essen Essen Germany
8 Division of Medical Physics in Radiology German Cancer Research Center Heidelberg Germany
2 Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen Essen Germany
7 The Netherlands Institute for Neuroscience, Royal Academy of Arts & Sciences Amsterdam The Netherlands
AuthorAffiliation_xml – name: 6 Department for Computer Science University of Western Ontario London Ontario Canada
– name: 1 Department of Neurology Essen University Hospital Essen Germany
– name: 8 Division of Medical Physics in Radiology German Cancer Research Center Heidelberg Germany
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Keywords delay conditioning
deep cerebellar nuclei
cerebellar imaging
associative learning
human
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2012; 107
2001; 21
1990; 83
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2014; 108
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2009; 32
1984b; 4
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Snippet Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction...
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SubjectTerms Adolescent
Adult
Analysis of Variance
associative learning
Aversion learning
Blinking - physiology
Brain
Brain Mapping
Cerebellar Cortex - diagnostic imaging
Cerebellar Cortex - physiology
cerebellar imaging
Cerebellar Nuclei - diagnostic imaging
Cerebellar Nuclei - physiology
Cerebellar plasticity
Cerebellum
Conditioning
Conditioning, Eyelid - physiology
deep cerebellar nuclei
delay conditioning
Extinction behavior
Extinction, Psychological - physiology
Eyelid conditioning
Female
Functional magnetic resonance imaging
Hum
human
Humans
Image processing
Learning
Magnetic resonance imaging
Magnetic Resonance Imaging - instrumentation
Male
Memory
Modulation
Neuroimaging
Neuropsychological Tests
Nuclei
Resonance
Serial learning
Unconditioned stimulus
Young Adult
Title Modulation of 7 T fMRI Signal in the Cerebellar Cortex and Nuclei During Acquisition, Extinction, and Reacquisition of Conditioned Eyeblink Responses
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.23641
https://www.ncbi.nlm.nih.gov/pubmed/28474470
https://www.proquest.com/docview/1915749472
https://www.proquest.com/docview/1896036517
https://pubmed.ncbi.nlm.nih.gov/PMC6866767
Volume 38
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