Literature DB >> 2718098

Classical conditioning in rabbits using pontine nucleus stimulation as a conditioned stimulus and inferior olive stimulation as an unconditioned stimulus.

J E Steinmetz1, D G Lavond, R F Thompson.   

Abstract

Classical conditioning of skeletal muscle responses was accomplished by pairing microstimulation of the pontine nuclei as a conditioned stimulus (CS) with microstimulation of the dorsal accessory olive as an unconditioned stimulus (US). A conditioned response identical in form to the behavioral response elicited by the olivary stimulation was established when the CS was forward paired with the US, and behavioral extinction occurred with CS-alone presentations or unpaired CS-US presentations. Conditioned responding could not be established or maintained when the CS and US were simultaneously presented or when the US preceded the CS (i.e., backward paired). Complete lesions of the interpositus nucleus abolished both conditioned and unconditioned responses. These findings support the idea that plasticity associated with classical conditioning of skeletal muscle responses occurs in regions of the cerebellum that receive convergent CS and US input.

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Mesh:

Year:  1989        PMID: 2718098     DOI: 10.1002/syn.890030308

Source DB:  PubMed          Journal:  Synapse        ISSN: 0887-4476            Impact factor:   2.562


  73 in total

1.  Developmental changes in eye-blink conditioning and neuronal activity in the inferior olive.

Authors:  D A Nicholson; J H Freeman
Journal:  J Neurosci       Date:  2000-11-01       Impact factor: 6.167

Review 2.  Ontogenetic changes in the neural mechanisms of eyeblink conditioning.

Authors:  J H Freeman; D A Nicholson
Journal:  Integr Physiol Behav Sci       Date:  2001 Jan-Mar

Review 3.  Parallel neural systems for classical conditioning: support from computational modeling.

Authors:  M T Allen; C E Myers; M A Gluck
Journal:  Integr Physiol Behav Sci       Date:  2001 Jan-Mar

4.  Central regulation of cerebellar climbing fibre input during motor learning.

Authors:  Richard Apps; Stephen Lee
Journal:  J Physiol       Date:  2002-05-15       Impact factor: 5.182

Review 5.  Exploring prefrontal cortical memory mechanisms with eyeblink conditioning.

Authors:  Craig Weiss; John F Disterhoft
Journal:  Behav Neurosci       Date:  2011-06       Impact factor: 1.912

6.  Synapse formation is associated with memory storage in the cerebellum.

Authors:  Jeffrey A Kleim; John H Freeman; Rochelle Bruneau; Brian C Nolan; Natalie R Cooper; Alison Zook; Drew Walters
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-16       Impact factor: 11.205

7.  Developmental changes in eyeblink conditioning and neuronal activity in the pontine nuclei.

Authors:  John H Freeman; Adam S Muckler
Journal:  Learn Mem       Date:  2003 Sep-Oct       Impact factor: 2.460

8.  Developmental changes in the neural mechanisms of eyeblink conditioning.

Authors:  John H Freeman; Daniel A Nicholson
Journal:  Behav Cogn Neurosci Rev       Date:  2004-03

Review 9.  Nothing can be coincidence: synaptic inhibition and plasticity in the cerebellar nuclei.

Authors:  Jason R Pugh; Indira M Raman
Journal:  Trends Neurosci       Date:  2009-01-27       Impact factor: 13.837

10.  Blockade of GABAA receptors in the interpositus nucleus modulates expression of conditioned excitation but not conditioned inhibition of the eyeblink response.

Authors:  Brian C Nolan; Daniel A Nicholson; John H Freeman
Journal:  Integr Physiol Behav Sci       Date:  2002 Oct-Dec
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