Literature DB >> 28474470

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

Thomas M Ernst1,2, Markus Thürling1,2, Sarah Müller1, Fabian Kahl1, Stefan Maderwald2, Marc Schlamann3,4, Henk-Jan Boele5, Sebastiaan K E Koekkoek5, Jörn Diedrichsen6, Chris I De Zeeuw5,7, Mark E Ladd2,8, Dagmar Timmann1.   

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. © 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  associative learning; cerebellar imaging; deep cerebellar nuclei; delay conditioning; human

Mesh:

Year:  2017        PMID: 28474470      PMCID: PMC6866767          DOI: 10.1002/hbm.23641

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


  73 in total

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Authors:  M D Mauk
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2.  Acquisition of eyeblink conditioning is critically dependent on normal function in cerebellar cortical lobule HVI.

Authors:  P J Attwell; S Rahman; C H Yeo
Journal:  J Neurosci       Date:  2001-08-01       Impact factor: 6.167

3.  Long-term depression at the mossy fiber-deep cerebellar nucleus synapse.

Authors:  Wei Zhang; David J Linden
Journal:  J Neurosci       Date:  2006-06-28       Impact factor: 6.167

4.  Acquisition, extinction, and reacquisition of a cerebellar cortical memory trace.

Authors:  Dan-Anders Jirenhed; Fredrik Bengtsson; Germund Hesslow
Journal:  J Neurosci       Date:  2007-03-07       Impact factor: 6.167

Review 5.  Distributed synergistic plasticity and cerebellar learning.

Authors:  Zhenyu Gao; Boeke J van Beugen; Chris I De Zeeuw
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Review 6.  Cerebellar mechanisms of learning and plasticity revealed by delay eyelid conditioning.

Authors:  Michael D Mauk; Wenke Li; Andrei Khilkevich; Hunter Halverson
Journal:  Int Rev Neurobiol       Date:  2014       Impact factor: 3.230

7.  A functional anatomical study of associative learning in humans.

Authors:  S E Molchan; T Sunderland; A R McIntosh; P Herscovitch; B G Schreurs
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8.  Learning- and expectation-related changes in the human brain during motor learning.

Authors:  N Ramnani; I Toni; O Josephs; J Ashburner; R E Passingham
Journal:  J Neurophysiol       Date:  2000-12       Impact factor: 2.714

9.  Contextual control of the extinction of conditioned fear: tests for the associative value of the context.

Authors:  M E Bouton; D A King
Journal:  J Exp Psychol Anim Behav Process       Date:  1983-07

10.  Evolving Models of Pavlovian Conditioning: Cerebellar Cortical Dynamics in Awake Behaving Mice.

Authors:  Michiel M ten Brinke; Henk-Jan Boele; Jochen K Spanke; Jan-Willem Potters; Katja Kornysheva; Peer Wulff; Anna C H G IJpelaar; Sebastiaan K E Koekkoek; Chris I De Zeeuw
Journal:  Cell Rep       Date:  2015-11-19       Impact factor: 9.423

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  7 in total

1.  Extinction and Renewal of Conditioned Eyeblink Responses in Focal Cerebellar Disease.

Authors:  Katharina M Steiner; Yvonne Gisbertz; Dae-In Chang; Björn Koch; Ellen Uslar; Jens Claassen; Elke Wondzinski; Thomas M Ernst; Sophia L Göricke; Mario Siebler; Dagmar Timmann
Journal:  Cerebellum       Date:  2019-04       Impact factor: 3.847

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Authors:  Xiaoming Du; Laura M Rowland; Ann Summerfelt; Fow-Sen Choa; George F Wittenberg; Krista Wisner; Andrea Wijtenburg; Joshua Chiappelli; Peter Kochunov; L Elliot Hong
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3.  Neural Substrates Underlying Eyeblink Classical Conditioning in Adults With Alcohol Use Disorders.

Authors:  Dominic T Cheng; Laura C Rice; Mary E McCaul; Jessica J Rilee; Monica L Faulkner; Yi-Shin Sheu; Joanna R Mathena; John E Desmond
Journal:  Alcohol Clin Exp Res       Date:  2020-02-16       Impact factor: 3.928

4.  The cerebellum is involved in processing of predictions and prediction errors in a fear conditioning paradigm.

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Authors:  Carlos Alexandre Gomes; Katharina M Steiner; Nicolas Ludolph; Tamas Spisak; Thomas M Ernst; Oliver Mueller; Sophia L Göricke; Franziska Labrenz; Winfried Ilg; Nikolai Axmacher; Dagmar Timmann
Journal:  Hum Brain Mapp       Date:  2021-01-07       Impact factor: 5.038

6.  Cerebellar Activation Deficits in Schizophrenia During an Eyeblink Conditioning Task.

Authors:  Nancy B Lundin; Dae-Jin Kim; Rachel L Tullar; Alexandra B Moussa-Tooks; Jerillyn S Kent; Sharlene D Newman; John R Purcell; Amanda R Bolbecker; Brian F O'Donnell; William P Hetrick
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7.  Functional Compartmentalization of the Contribution of Hippocampal Subfields to Context-Dependent Extinction Learning.

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  7 in total

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