Literature DB >> 2073949

Activity of deep cerebellar nuclear cells during classical conditioning of nictitating membrane extension in rabbits.

N E Berthier1, J W Moore.   

Abstract

The activity of neurons in the interposed and dentate nuclei of the cerebellum was investigated during differential classical conditioning of the rabbit eye blink nictitating membrane response. Forty-seven percent of the 165 cells in the study responded to the orbital stimulation used as the unconditioned stimulus (US). The latency distribution of US-elicited responses was bimodal with peaks at 7 and 19 ms. Twenty-one percent of the cells responded with short latencies to the tones used as conditioned stimuli (CSs). These cells typically responded to both the reinforced and nonreinforced CSs. Forty-one percent of the cells responded on conditioned response (CR) trials but not on trials without CRs. The average lead of the neural response to the CR was 71.4 ms. Cells that responded on CR trials were more likely to respond to the CSs, or to the CSs and the US, than cells that did not respond on CR trials. For about half of the cells that responded on CR trials the latency of response followed trial-by-trial variations of CR latency. For the remainder, the response was time-locked to CS-onset. Cells whose responses paralleled the CR may be involved in the initiation or modulation of the CR, while those whose responses were time-locked to the CS may be involved in sensory processing underlying the initiation of the movement. The pathways that may underlie the US- and CS-elicited responses are also discussed.

Entities:  

Mesh:

Year:  1990        PMID: 2073949     DOI: 10.1007/BF00232192

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  43 in total

1.  Responses of single units in cerebellar vermis of the cat to monaural and binaural stimuli.

Authors:  L M Aitkin; J Boyd
Journal:  J Neurophysiol       Date:  1975-03       Impact factor: 2.714

2.  Reacquisition of classical conditioning after removal of cerebellar cortex.

Authors:  D G Lavond; J E Steinmetz; M H Yokaitis; R F Thompson
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

3.  Frequency sensitivities of auditory neurons in the cerebellum of the cat.

Authors:  C M Huang; R Burkard
Journal:  Brain Res       Date:  1986-04-16       Impact factor: 3.252

4.  Activity of dentate neurons during arm movements triggered by visual, auditory, and somesthetic stimuli in the monkey.

Authors:  C E Chapman; G Spidalieri; Y Lamarre
Journal:  J Neurophysiol       Date:  1986-02       Impact factor: 2.714

5.  Fast ballistic arm movements triggered by visual, auditory, and somesthetic stimuli in the monkey. I. Activity of precentral cortical neurons.

Authors:  Y Lamarre; L Busby; G Spidalieri
Journal:  J Neurophysiol       Date:  1983-12       Impact factor: 2.714

6.  Acoustic input to the lateral pontine nuclei.

Authors:  L M Aitkin; J Boyd
Journal:  Hear Res       Date:  1978-10       Impact factor: 3.208

7.  Trigeminal primary afferents project bilaterally to dorsal horn and ipsilaterally to cerebellum, reticular formation, and cuneate, solitary, supratrigeminal and vagal nuclei.

Authors:  M F Jacquin; K Semba; R W Rhoades; M D Egger
Journal:  Brain Res       Date:  1982-08-26       Impact factor: 3.252

8.  Classical conditioning of the nictitating membrane response of the rabbit. I. Lesions of the cerebellar nuclei.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

9.  Fractured cutaneous projections to the granule cell layer of the posterior cerebellar hemisphere of the domestic cat.

Authors:  J Kassel; G M Shambes; W Welker
Journal:  J Comp Neurol       Date:  1984-05-20       Impact factor: 3.215

10.  Classical conditioning of the nictitating membrane response of the rabbit. IV. Lesions of the inferior olive.

Authors:  C H Yeo; M J Hardiman; M Glickstein
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

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  40 in total

1.  Developmental changes in eye-blink conditioning and neuronal activity in the cerebellar interpositus nucleus.

Authors:  J H Freeman; D A Nicholson
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

Review 2.  Classical eyeblink conditioning: clinical models and applications.

Authors:  J E Steinmetz; J A Tracy; J T Green
Journal:  Integr Physiol Behav Sci       Date:  2001 Jul-Sep

3.  Cerebellar cortical inhibition and classical eyeblink conditioning.

Authors:  Shaowen Bao; Lu Chen; Jeansok J Kim; Richard F Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

4.  fMRI of the conscious rabbit during unilateral classical eyeblink conditioning reveals bilateral cerebellar activation.

Authors:  Michael J Miller; Nan-kuei Chen; Limin Li; Brian Tom; Craig Weiss; John F Disterhoft; Alice M Wyrwicz
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

Review 5.  The role of interpositus nucleus in eyelid conditioned responses.

Authors:  J M Delgado-García; A Gruart
Journal:  Cerebellum       Date:  2002-12       Impact factor: 3.847

Review 6.  Using eyeblink classical conditioning as a test of the functional consequences of exposure of the developing cerebellum to alcohol.

Authors:  John T Green
Journal:  Integr Physiol Behav Sci       Date:  2003 Jan-Mar

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.  Timing and causality in the generation of learned eyelid responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Front Integr Neurosci       Date:  2011-08-30

9.  Dynamic changes in the cerebellar-interpositus/red-nucleus-motoneuron pathway during motor learning.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

10.  Lock-and-key mechanisms of cerebellar memory recall based on rebound currents.

Authors:  Daniel Z Wetmore; Eran A Mukamel; Mark J Schnitzer
Journal:  J Neurophysiol       Date:  2007-08-01       Impact factor: 2.714

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