Literature DB >> 18322108

Extinction of a classically conditioned response: red nucleus and interpositus.

Karla Robleto1, Richard F Thompson.   

Abstract

It is well established that the cerebellum and its associated circuitry are essential for classical conditioning of the eyeblink response and other discrete motor responses (e.g., limb flexion, head turn, etc.) learned with an aversive unconditioned stimulus. However, brain mechanisms underlying extinction of these responses are still relatively unclear. Behavioral studies have demonstrated extinction to be an active learning process distinct from acquisition. Accordingly, this current understanding of extinction has guided neural studies that have tried to identify possible brain structures that could support this new learning. However, whether extinction engages the same brain sites necessary for acquisition is not yet clear. This poses an overriding problem for understanding brain mechanisms necessary for extinction because such analysis cannot be done without first identifying brain sites and pathways involved in this phenomenon. Equally elusive is the validity of a behavioral theory of extinction that can account for the properties of extinction. In this study, we looked at the involvement of the interpositus and the red nucleus in extinction. Results show that, although inactivation of both nuclei blocks response expression, only inactivation of the interpositus has a detrimental effect on extinction. Moreover, this detrimental effect was completely removed when inactivation of the interpositus was paired with electrical stimulation of the red nucleus. These findings speak to the important role of cerebellar structures in the extinction of discrete motor responses and provide important insight as to the validity of a particular theory of extinction.

Mesh:

Year:  2008        PMID: 18322108      PMCID: PMC6671190          DOI: 10.1523/JNEUROSCI.4781-07.2008

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  12 in total

1.  Multiple sites of extinction for a single learned response.

Authors:  Brian E Kalmbach; Michael D Mauk
Journal:  J Neurophysiol       Date:  2011-09-21       Impact factor: 2.714

Review 2.  Spike-coding mechanisms of cerebellar temporal processing in classical conditioning and voluntary movements.

Authors:  Kenji Yamaguchi; Yoshio Sakurai
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

3.  Inactivation of the interpositus nucleus blocks the acquisition of conditioned responses and timing changes in conditioning-specific reflex modification of the rabbit eyeblink response.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Neurobiol Learn Mem       Date:  2018-07-24       Impact factor: 2.877

4.  Inactivation of the interpositus nucleus during unpaired extinction does not prevent extinction of conditioned eyeblink responses or conditioning-specific reflex modification.

Authors:  Lauren B Burhans; Bernard G Schreurs
Journal:  Behav Neurosci       Date:  2019-03-14       Impact factor: 1.912

5.  Comparison of auditory and visual conditioning stimuli in delay eyeblink conditioning in healthy young adults.

Authors:  Adam B Steinmetz; Chad R Edwards; Joseph E Steinmetz; William P Hetrick
Journal:  Learn Behav       Date:  2009-11       Impact factor: 1.986

6.  Neurobiological basis of failure to recall extinction memory in posttraumatic stress disorder.

Authors:  Mohammed R Milad; Roger K Pitman; Cameron B Ellis; Andrea L Gold; Lisa M Shin; Natasha B Lasko; Mohamed A Zeidan; Kathryn Handwerger; Scott P Orr; Scott L Rauch
Journal:  Biol Psychiatry       Date:  2009-09-12       Impact factor: 13.382

7.  Effects of extinction on classical conditioning and conditioning-specific reflex modification of rabbit heart rate.

Authors:  Lauren B Burhans; Carrie Smith-Bell; Bernard G Schreurs
Journal:  Behav Brain Res       Date:  2009-09-09       Impact factor: 3.332

Review 8.  BEHAVIORAL AND NEUROBIOLOGICAL MECHANISMS OF PAVLOVIAN AND INSTRUMENTAL EXTINCTION LEARNING.

Authors:  Mark E Bouton; Stephen Maren; Gavan P McNally
Journal:  Physiol Rev       Date:  2020-09-24       Impact factor: 37.312

9.  A reversal learning task detects cognitive deficits in a Dachshund model of late-infantile neuronal ceroid lipofuscinosis.

Authors:  D N Sanders; S Kanazono; F A Wininger; R E H Whiting; C A Flournoy; J R Coates; L J Castaner; D P O'Brien; M L Katz
Journal:  Genes Brain Behav       Date:  2011-08-07       Impact factor: 3.708

10.  Recruitment in retractor bulbi muscle during eyeblink conditioning: EMG analysis and common-drive model.

Authors:  N F Lepora; J Porrill; C H Yeo; C Evinger; P Dean
Journal:  J Neurophysiol       Date:  2009-08-12       Impact factor: 2.714

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